Skip to main content


Front. Chem., 24 July 2015
Sec. Crop Biology and Sustainability
Volume 3 - 2015 |

Seed dormancy is modulated in recently evolved chlorsulfuron-resistant Turkish biotypes of wild mustard (Sinapis arvensis)

Muhamet Topuz1,2 Yildiz Nemli2 Tahira Fatima1 Autar K. Mattoo1*
  • 1Sustainable Agricultural Systems Laboratory, Agricultural Research Service, United States Department of Agriculture, Henry A. Wallace Beltsville Agricultural Research Center, Beltsville, MD, USA
  • 2Plant Protection Research Station, Department of Plant Protection, Ege University, Izmir, Turkey

Biotypes of the broad-leaved wild mustard (Sinapis arvensis L.) found in wheat fields of Aegean and Marmara region of Turkey were characterized and shown to have developed resistance to sulfonylurea (chlorsulfuron), an inhibitor of acetolactate synthase (ALS). DNA sequence analysis of the ALS genes from two such resistant (“R”) biotypes, KNF-R1 and KNF-R2, revealed point mutations, CCT (Pro 197) to TCT (Ser 197) in KNF-R1 and CCT (Pro 197) to ACT (Thr 197) in KNF-R2; these substitutions are consistent with the presence of chlorsulfuron-insensitive ALS enzyme activity in the “R” S. arvensis biotypes. An additional phenotype of chlorsulfuron resistance in the Turkish S. arvensis “R” biotypes was revealed in the form of an altered seed dormancy behavior over 4–48 months of dry storage (after-ripening) compared to the susceptible (“S”) biotypes. Seeds of the “S” biotypes dry stored for 4 months had a higher initial germination, which sharply decreased with storage time, while the seeds of the “R” biotypes had lower germination after 4-months storage, rising sharply and peaking thereafter by 24 months' of dry storage. The “R” biotype seeds continued to maintain a higher germination percentage even after 48 months of after-ripening. The seed weight of “R” and “S” biotypes after-ripened for 4 months was similar but those after-ripened for 48 months differed, “R” seeds were significantly heavier than those of the “S” seeds. Differential seed germinability between “S” and “R” biotypes was found not a case of differential viability, temperature regimen or non-response to pro-germination hormone GA3. These studies are of relevance to ecological fitness of herbicide-resistant biotypes in terms of seed viability and germination.


Maximizing crop yields are vital for feeding the burgeoning population in the world. Major obstacles to increasing crop productivity include weed competition (as high as 100 billion dollars a year or even more), and maintaining seed vigor of the cash crop upon storage since seed germination decreases upon aging (Kocsy, 2015). For instance, wheat yield losses are proportional to increased weed density ($department/deptdocs.nsf/all/crop1280), since the latter compete for soil nutrients, water, space and light. Weeds have therefore been a major management constraint for agriculturists, farmers, and crop biologists alike. The discovery of sulfonylureas as inhibitors of acetolactate synthase (ALS) [EC], also known as acetohydroxyacid synthase (AHAS), which catalyzes the first committed step in the biosynthesis of branched-chain amino acids (valine, leucine, and isoleucine), led to sulfonylureas-based herbicides as effective weed management tool for a number of crops including wheat (Umbarger, 1978; Tranel and Wright, 2002).

Chlorsulfuron was formulated as an herbicide and introduced into agriculture worldwide over 30 years ago to control growth of monocot and dicot weed species. Its frequent use, however, led to weed resistant biotypes, such as prickly lettuce (Lactuca seriola L.) (Mallory-Smith et al., 1990) and kochia (Kochia scoparia L. Schrad.) (Primiani et al., 1990). The resistance to chlorsulfuron was linked to point mutation(s) in the ALS gene, which prevented herbicide binding to the ALS enzyme (Mallory-Smith et al., 1990; Martinez-Ghersa et al., 2000), as well as to enhanced ability to catabolize the herbicide (Primiani et al., 1990). By 2015, 246 plant species (103 monocots and 143 dicot) are reported to have developed resistance to ALS inhibitors (Heap, 2015).

The relevance of herbicide resistance is of tremendous concern for weed management including the possibility of their altered ecological fitness in regard to their growth, competitive ability and seed production and seed germination ability (Gressel and Segel, 1978; Tranel and Wright, 2002; Vila-Aiub et al., 2005). Little information is available on the fitness of chlorsulfuron-resistant weeds, although an early report found seeds of chlorsulfuron-resistant kochia biotype to germinate faster than the susceptible biotype (Dyer et al., 1993).

Wheat is grown in Turkey in ~9.4 m ha, occupying about 45% of the total arable land (FAOSTAT Database; The application of sulfonylurea herbicides has successfully managed weeds in Turkish agriculture (including wheat, rice, and maize cultivations) in the past for over 30 years. Among these weeds, wild mustard (Sinapis arvensis L.) is of noted importance causing substantial yield losses in wheat even when present at low seeding rate (60 plants/m2) (Gillespie and Nalewaja, 1988). Another study conducted on S. arvensis at seeding rates of 54 and 108 plants m−2 found 12–20 and 20–56% reductions in wheat yields, respectively ($department/deptdocs.nsf/all/crop1280).

S. arvensis is frequently observed in the wheat growing Aegean and Marmara region of Turkey (Boz, 2000; Topuz and Nemli, 2001). Two of its biotypes, called KNF-R1 and KNF-R2, were identified as being resistant to sulfonylurea application in the Bandırma-Balıkesir province of the latter wheat-growing region. Here, we characterize chlorsulfuron resistance in these Turkish S. arvensis biotypes at physiological and molecular levels, linking resistance to known mutation(s) in the ALS gene and a chlorsulfuron-insensitive ALS enzyme. Further, we show an additional phenotype of chlorsulfuron resistant S. arvensis biotypes in the form of an altered seed dormancy behavior compared to the susceptible biotypes. These studies are of relevance to ecological fitness of herbicide-resistant biotypes in terms of seed viability and germination.

Materials and Methods

Plant Material

Wild mustard (S. arvensis) seeds were collected from surviving weeds in wheat fields sprayed with chlorsulfuron in Bandırma-Balıkesir provinces of Marmara region (latitude 40° 19′ 6″ N and longitude 27° 58′ 40″ E), Turkey. Two resistant (R) biotypes (labeled as KNF-R1 and KNF-R2) were collected from wheat fields in Kulefli, ~4 km apart, about 8 km southwest of Bandırma airport. These fields had a history of chlorsulfuron applications for weed control for several years. Chlorsulfuron-susceptible (“S”) biotypes (labeled as MR-S biotype for herbicide resistance studies; and MR-S1 and MR-S2 for seed germination studies) were collected from ditch banks next to wheat fields from which KNF-R1 and KNF-R2 biotypes originated. Seeds of each biotype were collected from five plants, bulked, air dried at room temperature, and then stored at 4°C until use.

Whole Plant Herbicide Dose-Response Studies

Dose-response data for chlorsulfuron were generated from experiments carried out both in Turkey and the USA. The remaining experiments were performed solely in the USA. In Turkey, the experiments were carried out in open net houses covered by polyethylene at the Plant Protection Research Institute, Izmir/Bornova. The seeds were directly seeded in 20 × 20 × 20 cm pots containing turf (obtained after sieving decomposed tree leaf litter):soil:sand (2:1:1 ratio), at three plants per pot. Experiments in the USA were carried out in a temperature-controlled greenhouse at the USDA, Henry A. Wallace Beltsville Agricultural Research Center, Maryland (latitude 39° 1′ 39.35″ N and longitude 76° 55'35.40W). Seeds were sown in Metro-mix 360 (Scotts-Sierra Horticultural Products, Marysville, OH, USA) in plastic containers. At the cotyledon stage, the seedlings were transplanted into 10 × 10 × 10 cm plastic pots (1 plant per pot in quadruplicate) on the same media. Temperature regime was 21°C/16°C day/night with 16 h photoperiod supplemented with 230 μmol m2 s−1 illumination. Plants were watered daily and treated at 3–4 leaf stage with chlorsulfuron (Glean/Glean®) using a hand sprayer (Turkey) or pressurized sprayer (USA), both equipped with a flat fan nozzle (8001E), calibrated to deliver 300 L ha-1 of spray solution at 210 kPa. Chlorsulfuron was applied at rates (indicated in the text) that were 0.5–8 times the recommended application rates in Turkey (10 g a.i ha−1), and from 0.25 to 128 times in the USA based on a calculated minimum rate of 10 g a.i ha−1. The untreated controls were sprayed with water instead of the herbicide. The effects of the applied herbicides were evaluated 21 days after the treatment (DAT). The shoots were cut at soil level to collect the biomass, which was then air dried at 65°C for 72 h to determine dry weight. Plant pots were arranged in a randomized complete block design, with five replications in Turkey and four replications in USA, and experiments were repeated twice. Whole plant herbicide cross-resistance was studied with trifensulfuron-methyl (doses equivalent to 4.35, 8.7, 17.4, 34.8, and 69.6 g a.i ha−1; Harmony® GT, 750 g a.i kg-1, Du Pont). Chlorsulfuron resistant (KNF-R1 and KNF-R2) and susceptible (MR-S) biotypes were grown as described above and treated at the 3–4 leaf stage for cross resistance pattern for trifensulfuron-methyl. In all the experiments, untreated controls were sprayed with water. Herbicides were applied with a pressurized sprayer with a flat fan nozzle as described above.

Acetolactate Synthase (ALS) Enzyme Assay

Leaves were excised from the resistant KNF-R1 and KNF-R2, and susceptible MR-S S. arvensis biotypes, and processed for the preparation of cell-free extracts, protein precipitation with ammonium sulfate and desalting on Sephadex G-25 column as previously described (Ray, 1984). ALS [EC] activity was determined in 60% ammonium sulfate precipitated protein fraction (after desalting). Total protein content was determined by the Bradford method (Bradford, 1976). The ALS enzyme assay was carried out with slight modifications as previously described (Rashid et al., 2003). The reaction assay mixture contained, in a final volume of 500 μL, desalted (NH4)2SO4-precipitated protein (100 μg), 300 μL of the assay medium (83.3 mM potassium phosphate, pH 7.0, containing 167 mM sodium pyruvate,16.7 mM MgCl2,1.67 mM thiamine pyrophosphate and 16.6 μL FAD), and H2O or herbicide. The herbicide concentrations were varied from 0 to 100 nM. The reaction mixtures were incubated at 35°C for 60 min and the enzymatic reaction stopped by adding 50 μl of 6 N H2SO4. After incubation at 60°C for 15 min, 25 μl of 3N NaOH were added to each tube, and pH adjusted to 7.0. The samples were microfuged for 5 min. After adding 500 μl each of creatine (Sigma, C0780, 5.45 g l−1 in water) and 1-napthol (54.5 g l−1 in freshly prepared 2.5 N NaOH), the tubes were incubated at 60°C. The samples were microfuged for 1 min and then absorbance of the color developed was measured spectrophotometrically at 525 nm (Molecular Devices Spectra Max Plus384). The experiment was repeated 3 times.

ALS Gene Sequencing

Genomic DNA was extracted from young leaves, excised from a total of 5 plants from each biotype, as previously described (Delaporta et al., 1983) and quantified spectrophotometrically. The ALS gene from MR-S, KNF-R1, and KNF-R2 biotypes was PCR amplified and the PCR products sequenced to determine the sites where mutations may have arisen. Three overlapping regions were amplified using primer sets (Tan and Medd, 2002) (Table 1) and conditions as described (Warwick et al., 2005). The PCR amplification reaction contained 100 ng genomic DNA, primers (each 0.5 μM), 200 μM dNTP, 1.5 mM MgCl2 and 2 μl (5 units/μl) Go Taq® Flexi DNA Polymerase (Promega cat No: M8291) in a final volume of 100 μl. PCR products were separated on 1.5% low melting agarose gels and purified using Qiaquick® Gel Purification Kit (Qiagen, 28704). Direct cycle sequencing was outsourced to MWG, North Carolina (USA). Each PCR product was sequenced with both forward and reverse primers. Nucleotide and amino acid positions were numbered based on the amino acid sequence of ALS from Arabidopsis thaliana (Sathasivan et al., 1990).


Table 1. List of primers used to amplify the ALS gene of S. arvensis biotypes.

Seed Preparation for Germination Studies

Experiments carried out in the laboratory, growth chamber and greenhouse followed completely randomized design with four replications, and were repeated twice. Seeds were stored at 4°C for the times indicated in the text. Prior to use, seeds from S. arvensis resistant and susceptible biotypes were surface sterilized for 1 min in 70% ethanol followed by two 5 min immersions in 0.3% sodium hypochlorite and then thoroughly rinsed with sterile water (Yajima et al., 2004). The same seed lots and germination chambers were used throughout the germination assays.

In the laboratory, seeds were placed in 12-well petri dishes with 2 seeds per well (24 seeds petri-dish−1) on sterile double filter paper, previously moistened with sterile water (0.6 ml well−1). Dormancy and viability tests were carried out in the absence and presence of gibberellic acid (GA3) at 0.1–10 mM. GA3 was first dissolved in isopropyl alcohol, and then diluted with water to achieve indicated concentrations. Controls included sterile water. The petri dishes were sealed with parafilm and stored in the dark at 22°C ± 2 °C. Germination of seeds (aged 3 and 8 years) was assessed daily, in the dark, for 14 days; germinated seeds were counted and removed. Germination was defined as any seed where the seed coat was found broken and the radicle was visible.

For experiments carried out in a temperature-controlled greenhouse (Henry A. Wallace Beltsville Agricultural Research Center, MD), seeds were sown on Metro-mix 360 (Scotts-Sierra Horticultural Products, Marysville, OH) in plastic containers (36 seeds replicate−1), watered daily and germination evaluated for 21 days at 12 h intervals. Temperature regime was 21°C/16°C day/night with 16 h photoperiod supplemented with 230 μmol m2 s−1 illumination. The germinated seeds were counted and removed from the containers.

The effect of different temperature regimes (5, 10, and15°C) on seed germination was carried out in a growth chamber under 16 h light/8 h dark photoperiod.

Effect of After-Ripening Time on Seed Weight and Seed Germination Rate

Lots of 100 seeds each were randomly taken from two resistant (“R”) and two susceptible (“S”) biotypes for measuring weight of seeds that were dry-stored (after-ripening) for 4 months and 4 years. Seeds of (“R”) and (“S”) biotypes were evaluated for germination rates in a greenhouse taking seed lots stored for 4 months, 2 years, and 4 years (after-ripening time). Seeds were sown on Metro-mix 360 (Scotts-Sierra Horticultural Products, Marysville, OH) in plastic containers (36 seeds replicate−1), watered daily and germination evaluated for 21 days at 12 h intervals.

Statistical Analysis

The data on percentage of seeds that germinated on each plate were statistically analyzed using SPSS 15.0 for windows. Data were logarithmically transformed and then subjected to analysis of variance to determine the significance of differences between means at the 5% level of probability using the Duncan test. For further analysis, germinating seedlings were scored and converted to mean germination percentage and the standard errors of the means calculated. Dose-response curves (for chlorsulfuron) for the whole plant bioassay were plotted and statistically analyzed by SAS (1999) using a non-linear regression (Seefeldt et al., 1995) since seeds germinated at variable rates.


Establishing Herbicide Resistance in Turkish S. arvensis Biotypes

The shoot dry weight (SDW), used as a measure of growth response, of the sensitive (MR-S) and resistant (KNF-R1 and KNF-R2) Turkish S. arvensis biotypes to application of indicated doses of chlorsulfuron was tested both in Turkey (Figure 1A) and USA (Figure 1B). In Turkish trials, the MR-S biotype was found sensitive to the lowest applied chlorsulfuron dose while both the resistant biotypes, KNF-R1 and KNF-R2, were recalcitrant to chlorsulfuron concentrations as high as 80 g a.i ha−1. In the USA greenhouse experiments, chlorsulfuron levels used were higher, varying a thousand-fold (0–1280 g a.i ha−1). The MR-S biotype was found highly sensitive to the lowest herbicide concentration of 2.5 g a.i ha−1 as compared to its untreated control while the SDW of KNF-R1 and KNF-R2 biotypes was not affected up to a dose of 80 g a.i ha−1, as also seen in the Turkish trials (compare Figure 1B with Figure 1A). However, a progressive decrease in SDW was apparent even in KNF-R1 and KNF-R2 biotypes at chlorsulfuron concentration of 160 g a.i ha−1 and higher (Figure 1B).


Figure 1. Differential effects on the shoot dry weight (SDW) of wild mustard (S. arvensis) biotypes, MR-S (•), KNF-R1 (◦), and KNF-R2 (▾) in response to sprays with increasing concentrations of the ALS inhibitor, chlorsulfuron (A, B) or trifensulfuron-methyl (C) shown in log values. (A) Net-house in Izmir, Turkey; chlorsulfuron rates tested (0–80 g a.i.ha−1). Seeds used were dry-stored for 6–9 months. (B,C) Greenhouse at Beltsville, MD, USA; in (B) chlorsulfuron rates tested (0–320 g.a.i ha−1). Seeds used were dry stored for 24 months. Vertical bars represent standard error [n = 10, for (A,B); n = 8, for (C)].

Cross resistance of the three biotypes used here was also tested using other related herbicides - trifensulfuron-methyl (thifensulfuron), metsulfuron-methyl and imazamethabenz-methyl (IMI), and an unrelated herbicide 2,4-D (Jugulam et al., 2005). The MR-S biotype was found susceptible to all of these inhibitors while the KNF-R1 and KNF-R2 biotypes were found resistant also to the trifensulfuron-methyl (Figure 1C) but not to IMI, metsulfuron-methyl, or to the plant growth regulator 2,4-D (data not shown). The dose-response curves for trifensulfuron-methyl on the SDW of the three biotypes paralleled those obtained with chlorsulfuron (compare Figures 1A,B with Figure 1C).

Acetolactate Synthase Activity Isolated from Chlorsulfuron-Resistant S. arvensis Biotypes is Insensitive to Chlorsulfuron

Next, acetolactate synthase (ALS) activity was determined in the 60% ammonium sulfate precipitated protein fraction of soluble leaf extracts from KNF-R1, KNF-R2, and MR-S biotypes in the absence and presence of chlorsulfuron (Figure 2A). The ALS enzyme activity isolated from MR-S biotype was found sensitive to low concentrations of chlorsulfuron, 5 nM herbicide causing 50% inhibition of the enzyme activity. In contrast, ALS enzyme activity isolated from KNF-R1 and KNF-R2 biotypes was completely insensitive to chlorsulfuron, even at concentrations as high as 100 nM (Figure 2A). These in vitro data complement the in vivo dose response on the SDW of the three biotypes, and relate chlorsulfuron resistance of KNF-R1 and KNF-R 2 S. arvensis biotypes to an altered ALS protein.


Figure 2. (A) Acetolactate synthase (ALS) activity of resistant biotypes, KNF-R1 and KNF-R2, is not inhibited by chlorsulfuron. (B) Nucleotide positions, amino acids and ALS gene mutations in S. arvensis “R” biotypes, KNF-R1 and KNF-R2, in comparison to the “S” biotype MR-S using A. thaliana als sequence as standard. (C) Representation of the sequences around the mutation in ALS gene of “R” biotypes which results in amino acid substitution. In KNF-R1, the mutation C–T represents Pro197 (CCT) to Ser (TCT) substitution while in KNF-R2 the C–A change representing Pro197 (CCT) to Thr (ACT) substitution. The ALS gene from susceptible MR-S biotype did not harbor any of these mutations.

ALS Gene from Chlorsulfuron-resistant S. arvensis Biotypes Harbors Mutations

To test our contention that the ALS protein in KNF-R1 and KNF-R2 S. arvensis biotypes is altered, we carried out molecular analysis by first amplifying the ALS genes of all the three biotypes using PCR, and then the PCR products were sequenced. The sequences we obtained lacked 62–64 nucleotides from the 5′ end of the gene but included all the regions of the ALS gene previously shown to have mutations that confer resistance to chlorsulfuron (Tranel and Wright, 2002). Overall, DNA sequence analysis showed a total of 16 nucleotide mutations among the S. arvensis biotypes, fourteen of which were determined to be silent, i.e., when translated these did not result in a change in the amino acid (Figures 2B,C). ALS gene sequences varied slightly among the three biotypes, with some polymorphism being apparent (Figure 2C). The ALS gene of Turkish S. arvensis biotypes showed ~1% polymorphism, similar to that detected previously (Warwick et al., 2005). Amino acid substitution of Glu290 (GAG) to Ser290 (AGT) in MR-S biotype and Gly290 (GGT) in KNF-R1 and KNF-R2 biotypes was apparent but this amino acid change in ALS gene is not known to be associated with resistance phenomenon and is highly variable (Warwick et al., 2005). Notably, the single point mutation that resulted in an amino acid substitution was found at nucleotide position 589 in the ALS gene from “R” biotypes, KNF-R1 and KNF-R2 (Figure 2C). In the KNF-R1 ALS gene, the mutation C to T represents Pro197 (CCT) to Ser (TCT) substitution while in KNF-R2 the C to A change represents Pro197 (CCT) to Thr (ACT) substitution (Figure 2C). The ALS gene from susceptible MR-S biotype did not show any of these mutations (Figure 2C).

Chlorsulfuron-Resistant Turkish S. arvensis Biotypes are Altered in Seed Dormancy Behavior

Seed dormancy, germination, and emergence are important agronomic characteristics of weeds, which play a key role in agricultural productivity, determining competition and success of a staple crop and its weeds in an agroecosystem (Koger et al., 2004; Weitbrecht et al., 2011). Occasional reference to a possible link between herbicide resistance and seed dormancy has appeared in the literature but data are less dense. Therefore, we tested whether newly evolved chlorsulfuron resistance of S. arvensis, associated with altered ALS gene/enzyme, has any impact on the seed germination ability as compared to the sensitive biotypes.

Over a few years during which these studies were conducted, we consistently observed variability in the germination rate of seeds of chlorsulfuron susceptible (S) vs. resistant (R) S. arvensis biotypes. Therefore, we carried out controlled, long-term experiments (in the USA) and compared seed germination rates of S. arvensis (“R”) and (“S”) biotypes after a period of 4 months, and after 2 and 4 years of dry storage. The seeds of “S” biotypes, MR-S1 and MR-S2, dry stored for 4-months had, respectively, a germination rate of 38.0 and 23.0% (Figure 3A), which decreased to 8 and 18% at 2 years (Figure 3B), and after 48-months' dry storage it was 13 and18.5% (Figure 3C). In contrast, the resistant biotypes, KNF-R1 and KNF-R2, showed an opposite germination trend to that of “S” biotypes. The germination rate of 4-months dry stored seeds of R1 and R2 biotypes was, respectively, 12.5 and 30.5% (Figure 3A), which increased to 68.0 and 56.7% at 2 years of storage (Figure 3B), and by 4 years of dry storage period it was 66.5 and 32.2% (Figure 3C). It is noted here that the seeds of “R” biotypes dry stored for 4 years germinated 24 h sooner than the “S” biotypes.


Figure 3. Cumulative seed germination (%) in relation to progressive emergence of S. arvensis chlorsulfuron-resistant “R” [KNF-R1 (∇), KNF-R2 (▾)], and susceptible “S” [MR-S1 (•) and MR-S2 (◦)] biotype seeds. Seeds used were dry stored for: (A), 4 months; (B), 2 years (24 months); (C), 4 years (48 months). Vertical bars represent standard error (n = 6).

To further confirm the results from experiments carried out in the greenhouse, we compared germination of seeds from the “S” and “R” biotypes, dry stored for 2-3 years, at room temperature in the laboratory and at 22°C in the greenhouse. In the laboratory experiments, significantly higher percentage (74–75%) of seeds from “R” biotypes, KNF-R2 and KNF-R1, germinated compared to low % germination (26.9–27.1%) of “S” biotype counterparts, MR-S2 and MR-S1 (Figure 4A). A similar germination pattern was observed under controlled greenhouse conditions where germination of “R” biotypes was 81.9 and 75.0% in KNF-R1 and KNF-R2, respectively, compared to respective 26.8 and 24.3% in MR-S1 and MR-S2 (Figure 4B).


Figure 4. Cumulative seed germination (%) of S. arvensis chlorsulfuron-resistant “R,” KNF-R1 and KNF-R2, vs. susceptible “S” biotypes, MR-S1 and MR-S2, under controlled laboratory (A) and greenhouse conditions (B). In both tests, seeds used had been dry stored for 2–3 years. Vertical bars represent standard error [n = 12 for (A); n = 6 for (B)].

Different Seed Germination Potential of “S” and “R” S. arvensis Biotypes is not Altered by Suboptimal Temperature Regime

We next investigated if low temperature regime—5, 10, and 15°C—altered the germination potential of the “S” and “R” biotypes. These experiments were performed in a temperature-controlled growth chamber using seeds that had undergone dry storage for between 2.2 and 3 years. At 5°C, seeds from neither S. arvensis “R” and “S” biotypes germinated (data not shown). However, at both 10°C and 15°C the maximum cumulative germination was clearly advantageous in favor of “R” compared to “S” biotypes, being, respectively, 48.2–63.8% (10°C) and 50.0–53.2% (15°C) in “R” biotypes vs. 15.9–17.5% (10°C) and 29.1–30.7% (15°C) in “S” biotypes (Figures 5A,B; Supplemental Figure 1).


Figure 5. Emerging progression of chlorsulfuron-resistant “R,” KNF-R1 (∇) and KNF-R2 (▾), and susceptible “S,” MR-S1 (•) and MR-S2 (◦), S. arvensis biotypes sowed in a growth chamber held constant at 10°C (A) and 15°C (B). Cumulative seed germination (%) is presented as supplemental material (Supplemental Figure 1). Seed lots used had been dry-stored for 30–36 months. Vertical bars represent standard error (n = 6).

Differential Seed Germination of “S” and “R” S. arvensis Biotypes is not a Question of Seed Viability or Weight Difference

Seed weight of S. arvensis “S” and “R” biotypes measured after dry storage (after-ripened) of 4 months and 4 years are given in Figures 6A,B, respectively. The 4-months dry stored seeds from both lines had similar weight. However, seeds of “S” biotype dry stored for 4 years weighed lesser than the 4-month stored seeds (compare Figure 6B with A, MR-S1 and MR-S2) whereas during the same duration in dry storage, the “R” biotypes weighed more, being significantly heavier than their “S” counterparts (Figures 6A,B).


Figure 6. Mean seed mass of S. arvensis susceptible (MR-S1 and MR-S2) and resistant (KNF-R1 and KNF-R2) biotypes after 4 months (A) and 4 years (48 months) (B) of dry storage. Vertical bars represent standard error (n = 3; 100 seeds in 3 batches from each of the four biotypes were weighed).

To further ensure that the seeds of both “S” and “R” biotypes were viable, we tested the effects of a range, low to high concentrations, of the plant hormone gibberellic acid (GA3) on germination of seeds stored for 3 and 8 years. GA3 application to “S” biotype seeds dry stored for 3 years effectively increased their ability to germinate, raising it from 38.8% without GA3 to ~80% and higher at 1–5 mM GA3 reaching % germination value close to the untreated “R” biotype seeds (Figure 7A). Since we had the “S” and “R” biotypes in dry storage for 8 years, we also compared the effects of GA3 on them as well, especially because we had noted a decreasing trend in the germination of even the “R” biotype seeds dry stored for 4 years (see Figure 3C). By 8 years of dry storage, the germination rate of untreated seeds of MR-S2 biotype and KNF-R2 biotype was ~8 and ~26%, respectively. Both these biotypes responded to GA3 treatment by vigorous germination that increased with each higher dose of the GA3 (Figure 7B). The concentration of GA3 required to generate maximal effect on germination potential in these biotypes was found to vary, 5 mM was saturating for “R” biotype while 10 mM was optimal for the “S” biotype—the curve for “S” biotype, however, had not reached saturation (Figure 7B).


Figure 7. Gibberellic acid (GA3) application restores seed germination potential in chlorsulfuron-susceptible S. arvensis biotypes. (A) MR-S1 (open bars) and MR-S2 (serrated bars). Germination (%) of chlorsulfuron-resistant seeds (KNF-R1 and KNF-R2) is shown in “Control” next to the “S” biotypes. Seeds used in (A) had been dry stored for 3 years. In (B) the response curves to increasing concentrations of GA3 are shown with seeds of MR-S2 (■) and KNF-R2 (□) S. arvensis biotypes dry stored for 8 years. Vertical bars represent standard error (n = 3).


Wild mustard (S. arvensis L.) is a prolific weed in wheat fields, causing substantial yield loss to the crop. Field management for S. arvensis has involved the use of chlorsulfuron herbicides that inhibit acetolactate synthase (ALS) and impair the synthesis of three prominent branched-chain amino acids—valine, leucine, and isoleucine (as stated in the Introduction). However, resistance to this herbicide among weeds has been observed worldwide and generally attributed to amino acid substitutions in the ALS gene (Guttieri et al., 1992; Boutsalis et al., 1999; Gressel, 2002). Weed populations exposed to single-mechanism based herbicides that have longer residual life in the soil develop resistance and, in turn, can incur a fitness cost (Coustau et al., 2000; Tranel and Wright, 2002). The chlorsulfuron-resistant biotypes studied here originated from areas in Turkey, where wheat is mainly grown as a monoculture or in rotation with sunflower. These fields had a history of several years' consecutive use of the chlorsulfuron herbicide. We show and confirm that resistance to chlorsulfuron [ALS (AHAS)-inhibiting herbicides] in Turkish biotypes is associated with altered target site mutations in the ALS gene, corresponding to amino acid substitutions, Pro197 (CCT) to Ser (TCT), or Thr (ACT), as is known for many other species. These findings are consistent with our in vitro experiments showing that ALS enzyme activity in S. arvensis KNF-R1 and KNFR-2 biotypes, and not the susceptible biotypes, is insensitive to chlorsulfuron. The Pro to Ser (ALS from KNF-R1 biotype) or Thr (ALS from KNF-R2 biotype) substitutions are consistent with previously reported Pro substitution to Ser in Corn poppy (Papaver rhoeas L.) (Prado et al., 2004) and wild mustard (S. arvensis L.) (Warwick et al., 2005), Ala, Arg, Gln, Leu, Lys, Met, Ser, Thr, or Trp in Kochia (K. scoparia L.) (Guttieri et al., 1995; Warwick et al., 2008), or Ala/Thr in wild radish (R. raphanistrum L.) (Tan and Medd, 2002).

The newly evolved chlorsulfuron-resistant S. arvensis biotypes with mutated ALS gene became a resource to delineate effects on seed germination and weight in comparison to the susceptible biotypes. Interestingly, the time in dry storage (after-ripening) had a major and differential effect on the germinability of seeds from susceptible vs. resistant S. arvensis biotypes. The maximum cumulative germination was found to be different between “R” and “S” seeds after dry storage periods from 4 months to 4 years. Seeds from both biotypes held for 4 months in dry storage showed the “S” biotype seeds to record a higher germination than the seed from “R” biotype. However, as the dry storage period was prolonged the germinability of S biotype seeds sharply decreased with longer storage time. Surprisingly, the seeds from “R” biotypes recorded highest germination potential at 24 months dry storage, which slightly dropped at 4 years of dry storage and yet was significantly higher than the “S” biotype seeds. These data on variable germinability of S. arvensis being linked to the different biotypes may explain the diverse data on seed germination of this species in the literature. For example, a study on S. arvensis seeds immediately after harvest found quite low (7.2%) germinability compared to 28% in those stored for a year (Donald and Hoerauf, 1985), while in another study (Andersson and Milberg, 1998) S. arvensis seed germination varied as much as 20–90%. Although it is known that seed dormancy determines germination timing, little is known about how this process is regulated (Xiang et al., 2014).

Differential seed germinability between “S” and “R” biotypes was not due to differential viability, temperature regimen, or non-responsiveness to pro-germination hormone GA3, and likely associated with the “R” biotype phenotype due to single amino acid substitution, Pro197 (CCT) to Ser (TCT) or Thr (ACT), in the ALS gene. Thus, while the S. arvensis seeds dry stored for 4 months weighed the same irrespective of being sensitive (“S”) or resistant (“R”) to chlorsulfuron, however, after dry storage for 4 years the “R” seeds were significantly heavier than the “S” ones. Interestingly, seed weight and seed germination potential of “S” biotypes apparently correlated—as the seed weight was lost, the germination capacity also decreased. The “R” biotype seeds showed higher germination capacity at 10 and 15°C than the seeds of “S” biotype. This observation bodes well for the fitness of “R” biotype seeds since wild mustard germinates in two flushes, one in spring and the other in autumn both periods of cooler temperatures (Edwards, 1980).

Final evidence for the viability of “S” biotype seeds came from the response pattern of their germination upon application of GA3. GA3 treatment of “S” biotype seeds dry stored for 36 months resulted in high germinability, reaching a capacity near to that seen with untreated “R” biotype seeds. A comparison of germinability of “S” and “R” biotype seeds dry stored for 8 years demonstrated similar response to exogenous GA3, the “R” biotype seed germination saturating at 5 mM GA3 while the “S” biotype seeds showed a linear response which appeared to lead them to match the potential of the “R” seeds. Application of the GA3 antagonist in seed germination, abscisic acid (ABA), to “R” biotype seeds inhibited their germination (data not shown), suggesting that the germination differences between the two types of seeds may be due to differences in the endogenous ratio of ABA/GA3. In preliminary studies, ABA concentrations in the seeds of MR-S1 and MR-S2 S. arvensis biotypes were found to be 143–237% higher than the corresponding “R” biotype seeds (unpublished data). However, this remains to be further established. Thus, the ABA/GA hormone postulate (Karssen and Laçka, 1986) might apply to the differential seed germination between “S” and “R” biotypes of S. arvensis. In this regard, it is known that GA application is necessary to break dormancy in wild mustard germination (Karssen and Laçka, 1986; Duran and Retamal, 1989). These results are consistent with the findings on chlorsulfuron-resistant lettuce (Lactuca sativa L.), where the “R” near-isogenic line showed faster germination than the “S” line (Mallory–Smith et al., 1992), and on Bromus tectorum “R” biotypes, which germinated earlier than the “S” biotypes at low temperature (5°C); however, no differences in germination occurred at higher temperatures (Park et al., 2004).

The observation that the S. arvensis “R” biotype seeds were significantly heavier than those from the “S” biotypes upon dry storage for 4 years might seem intriguing. However, in this regard it is interesting to note that recent molecular studies with “dry” quiescent seeds showed the latter to be metabolically active as revealed by transcriptomics and protein dynamics (Leubner-Metzger, 2005). Surprisingly, dynamic processes within “dry” seed seem to characterize germination potential, with after-ripening being associated with specific gene networks (Carrera et al., 2008). Further, there is sparse information on post-transcriptional regulation and post-translational modification of proteins in dry seeds, which need to be addressed to throw light on the (molecular) mechanisms that regulate after-ripening (Holdsworth et al., 2007).

Studies on the environmental factors on seed germination/emergence are important for predicting when weeds in the growing season might emerge in order to put an effective weed management in place. To improve their competitive ability in agricultural farms, it is thought that annual weeds adjust the timing and rate of seed germination (Martinez-Ghersa et al., 2000). The degree of competition between the weed and the crop is dependent upon the relative time of their emergence, whichever germinates or emerges first is expected to have the upper hand by employing more time to establish and gainfully compete for space, light, and nutrients over the other (Neve et al., 2003).

The Turkish chlorsulfuron-resistant S. arvensis biotypes studied here have the ability to germinate faster in high percentages at cold temperature regimes, and sustain their germinability over a long dry storage time compared to their susceptible counterparts. It would imply that these resistant weeds would be more competitive in the field conditions compared to “S” biotypes. Rapid germination at low temperatures may be a characteristic trait associated with ALS target site resistance (Pro-197/-Ser/-Arg/-Thr), which was postulated to turn into either a fitness advantage or disadvantage depending upon the prevailing agroecological conditions (Park et al., 2004). Moreover, the rapid and high rates of seed germination of chlorsulfuron (ALS inhibitor) resistant S. arvensis “R” biotypes could also be “successfully” exploited in weed management strategies to safeguard the crop by draining the “R” weed seed bank. Relative fitness studies on other weeds have shown that the ALS “R” biotypes are not associated with growth penalty, rather under some conditions they may have fitness advantages compared to “S” biotypes (Gressel and Segel, 1990; Maxwell et al., 1990; Thomson et al., 1994; Christoffoleti et al., 1997). Data presented here on comparative seed germination between “R” and “S” biotypes of S. arvensis suggest that the altered target site trait conferring resistance to ALS inhibitor, chlorsulfuron in particular, in “R” biotypes does not result in a growth penalty.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


We thank Mary Camp (USDA-ARS Beltsville,Md) for statistical analysis of the data, Dr. Ahmet Uludağ for technical advice on some dose-response experiments, Prof. Jonathan Gressel for creative discussions, Dr. Vijaya Shukla for help with gene sequence submissions to Genbank, and Dr. Steven Mirsky and Dr. Bhavneet Kaur for constructive comments on the manuscript. The accession numbers of the ALS gene sequences deposited in Genbank are: MR-S (FJ655877), KNF–R1 (FJ655876), KNF-R2 (FJ 655875). Mention of trade names or commercial products in this article is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture (USDA). USDA is an Equal Opportunity Provider and Employer.

Supplementary Material

The Supplementary Material for this article can be found online at:


Andersson, L., and Milberg, P. (1998). Variation in seed dormancy among plants, populations and years of seed collection. Seed Sci. Res. 8, 29–38.

Google Scholar

Boutsalis, P., Karotam, J., and Powles, S. B. (1999). Molecular basis of resistance to acetolactate synthase-inhibiting herbicides in Sisymbrium orientale and Brassica tournefortii. Pesticide Sci. 55, 507–516.

Google Scholar

Boz, Ö. (2000). The determination of the weed species and their density and frequency in the wheat areas of Aydın province. J. Turk. Weed Sci. 3, 1–11.

Bradford, M. M. (1976). A rapid and sensitive method for the quantification of microgram quantities of protein using the principle of protein-dye binding. Anal. Biochem. 72, 248–252.

PubMed Abstract | Google Scholar

Carrera, E., Holman, T., Medhurst, A., Dietrich, D., Footitt, S., Theodoulou, F. L., et al. (2008). Seed after-ripening is a discrete developmental pathway associated with specific gene networks in Arabidopsis. Plant J. 53, 214–224. doi: 10.1111/j.1365-313X.2007.03331.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Christoffoleti, P. J., Westra, P., and Moore, F. (1997). Growth analysis of sulfonylurea resistant and susceptible kochia (Kochia scoparia). Weed Sci. 45, 691–695.

Google Scholar

Coustau, C., Chevillon, C., and French-Constant, R. (2000). Resistance to xenobiotics and parasites: can we count the cost? Trends Ecol Evol. 15, 378–383. doi: 10.1016/S0169-5347(00)01929-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Delaporta, S. L., Wood, J., and Hicks, J. B. (1983). A plant DNA minipreparation. Plant Mol. Biol. 1, 19–21.

Google Scholar

Donald, W. W., and Hoerauf, R. (1985). Enhanced germination and emergence of dormant wild mustard (S. arvensis) seed by two substituted phthalimides. Weed Sci. 33, 894–902.

Google Scholar

Duran, J. M., and Retamal, N. (1989). Coat structure and regulation of dormancy in Sinapis arvensis L. seeds. J. Plant Physiol. 135, 218–222.

Google Scholar

Dyer, W. E., Chee, P. W., and Fay, P. (1993). Rapid germination of sulfonylurea–resistant Kochia scoparia accessions is associated with elevated seed levels of branched-chain amino acids. Weed Sci. 41, 18–22.

Google Scholar

Edwards, M. M. (1980). Aspects of the population ecology of charlock. J. Appl. Ecol. 17, 151–172.

Google Scholar

Gillespie, G. R., and Nalewaja, J. D. (1988). Economic control of weeds in wheat, Triticum aestivum. Weed Technol. 2, 257–261

Google Scholar

Gressel, J. (2002). Molecular Biology of Weed Control. London: Taylor & Francis.

Google Scholar

Gressel, J., and Segel, L. A. (1978). The paucity of plants evolving genetic resistance to herbicides: possible reasons and implications. J. Theor. Biol. 75, 349–371.

PubMed Abstract | Google Scholar

Gressel, J., and Segel, L. A. (1990). Modeling the effectiveness of herbicide rotations and mixtures as strategies to delay or preclude resistance. Weed Tecnol. 4, 186–198.

Google Scholar

Guttieri, M. J., Eberlein, C. V., Mallory-Smith, C. A., Thill, D. C., and Hoffman, D. L. (1992). DNA sequence variation in Domain A of the acetolactate synthase genes of herbicide-resistant and -susceptible weed biotypes. Weed Sci. 40, 670–676.

Google Scholar

Guttieri, M. J., Eberlein, C. V., and Thill, D. C., (1995). Diverse mutations in the acetolactate synthase gene confer chlorsulfuron resistance in Kochia (Kochia scoparia) biotypes. Weed Sci. 43, 175–178.

Google Scholar

Heap, I. (2015). The International Survey of Herbicide Resistant Weeds. Available online at:

Holdsworth, M. J., Finch-Savage, W. E., Grappin, P., and Dominique, J. (2007). Post-genomics dissection of seed dormancy and germination. Trends Plant Sci. 13, 7–13. doi: 10.1016/j.tplants.2007.11.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Jugulam, M., Mclean, M. D., and Hall, J. C. (2005). Inheritance of picloram and 2,4-D resistance in wild mustard (Brassica kaber). Weed Sci. 53, 417–423. doi: 10.1614/WS-04-149R

CrossRef Full Text | Google Scholar

Karssen, C. M., and Laçka, E. (1986). “A revision of hormone balance theory of seed dormancy: studies on gibberellin and/or abscisic acid-deficient mutants of Arabidopsis thaliana,” in Plant Growth Substances, ed M. Bopp (Berlin: Springer-Verlag), 315–323.

Kocsy, G. (2015). Die or survive? – redox changes as seed viability markers. Plant Cell Environ. 38, 1008–1010. doi: 10.1111/pce.12515

PubMed Abstract | CrossRef Full Text | Google Scholar

Koger, C. H., Reddy, N., and Poston, D. H. (2004). Factors affecting seed germination, seedling emergence, and survival of texasweed (Caperonia palustris). Weed Sci. 52, 989–995. doi: 10.1614/WS-03-139R2

CrossRef Full Text | Google Scholar

Leubner-Metzger, G. (2005). β-1,3-glucanase gene expression in low hydrated seeds as a mechanism for dormancy release during tobacco after-ripening. Plant J. 41, 133–145. doi: 10.1111/j.1365-313X.2004.02284.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Mallory–Smith, C. A., Thill, D. C., Alcocer-Ruthling, M., and Thomson, C. (1992). “Growth comparisons of sulfonylurea resistant and susceptible biotypes,” in Proceedings of the First International Weed Control Congress, Vol. 2 (Melbourne, VIC: Weed Science Society of Victoria), 301–303.

Mallory-Smith, C. A., Thill, D. C., and Dial, M. J. (1990). Identification of sulfonylurea herbicide resistant prickly lettuce (Lactuca seriola). Weed Technol. 4, 163–168.

Google Scholar

Martinez-Ghersa, M. A., Ghersa, C. M., Benech-Arnold, R. L., Mac Donough, R., and Sanches, R. A. (2000). Adaptive traits regulating dormancy and germination of invasive plants. Plant Species Biol. 15, 127–137. doi: 10.1046/j.1442-1984.2000.00033.x

CrossRef Full Text | Google Scholar

Maxwell, B. D., Roush, M. L., and Radosevich, S. R. (1990). Predicting the evaluation and dynamics of herbicide resistance in weed populations. Weed Technol. 2–13.

PubMed Abstract | Google Scholar

Neve, P., Diggle, A. J., Smith, F. P., and Powles, S. B. (2003). Simulating evolution of glyphosate resistance in Lolium rigidum I: population biology of a rare resistance trait. Weed Res. 43, 404–417. doi: 10.1046/j.0043-1737.2003.00358.x

CrossRef Full Text | Google Scholar

Park, K. W., Mallory-Smith, C. A., Ball, D. A., and Mueller-Warrant, G. (2004). Ecological fitness of acetolactate synthase inhibitor-resistant and susceptible downy brome (Bromus tectorum) biotypes. Weed Sci. 52, 768–773. doi: 10.1614/WS-04-081R

CrossRef Full Text | Google Scholar

Prado, D. M., Osuna, D. M., Prado, R. D., and Franco, A. R. (2004). Molecular basis of resistance to sulfonylureas in Papaver rhoeas. Pesticide Biochem. Physiol. 79, 10–17. doi: 10.1016/j.pestbp.2004.01.003

CrossRef Full Text | Google Scholar

Primiani, M., Cotterman, M. J. C., and Saari, L. L. (1990). Resistance of kochia (Kochia scoparia) to sulfonylurea and imidazolinone herbicides. Weed Technol. 4, 169–172.

PubMed Abstract | Google Scholar

Rashid, A., Newman., J. C., O'Donovan, J. T., Robinson, D., Maurice, D., et al. (2003). Sulfonylurea herbicide resistance in Sonchus asper biotypes in Alberta, Canada. Weed Res. 43, 214–220. doi: 10.1046/j.1365-3180.2003.00336.x

CrossRef Full Text | Google Scholar

Ray, T. B. (1984). Site of action of chlorsulfuron. Plant Physiol. 75, 827–831.

PubMed Abstract | Google Scholar

SAS. (1999). Statistical Analysis Systems, SAS/STAT User's guide, Version 8. Cary, NC: Statistical Analysis Systems Institute.

Sathasivan, K., Haughn, G. W., and Murai, N. (1990). Nucleotide sequence of a mutant acetolactate synthase gene from an imidazolinone-resıstant Arabidopsis thaliana var. Columbia. Nucleic Acids Res. 18, 2188.

PubMed Abstract | Google Scholar

Seefeldt, S. S., Jensen, J. E., and Fuerst, E. P. (1995). Log-logistic analysis of herbicide dose-response relationships. Weed Technol. 9, 218–227.

Google Scholar

Tan, M. K., and Medd, R. W. (2002). Characterisation of the acetolactate synthase (ALS) gene of Raphanus raphanistrum L. and the molecular assay of mutations associated with herbicide resistance. Plant Sci. 163, 195–205. doi: 10.1016/S0168-9452(02)00082-1

CrossRef Full Text | Google Scholar

Thomson, C. R., Thill, D. C., and Shafii, B. (1994). Germination characteristics of sulfonylurea resistant and susceptible Kochia scoparia. Weed Sci. 42, 172–179.

Topuz, M., and Nemli, Y. (2001). Preliminary Studies on the Density of some Important Weed Seed Species in the Soil and Determination of the Relationship Between Soil Seed Bank and Weed Flora in Cereal Areas of Manyas (Balıkesir) Province. M.Sc. Thesis (2000), Ege University, Izmir.

Tranel, P. J., and Wright, T. R. (2002). Resistance of weeds to ALS-inhibiting herbicides: what have we learned? Weed Sci. 50, 700–712. doi: 10.1614/0043-1745(2002)050[0700:rrowta];2

CrossRef Full Text | Google Scholar

Umbarger, H. E. (1978). Amino acid biosynthesis and its regulation. Ann. Rev. Biochem. 47, 533–606.

PubMed Abstract | Google Scholar

Vila-Aiub, M. M., Neve, P., Steadman, K. J., and Powles, S. B. (2005). Ecological fitness of a multiple herbicide-resistant Lolium rigidum population; dynamics of seed germination and seedling emergence of resistance and susceptible phenotypes. J. Appl. Ecol. 42, 288–298. doi: 10.1111/j.1365-2664.2005.01017.x

CrossRef Full Text | Google Scholar

Warwick, S. I., Sauder, C., and Beckie, H. J. (2005). Resistance in Canadian biotypes of wild mustard (Sinapis arvensis) to acetolactate synthase inhibiting herbicides. Weed Sci. 53, 631–639. doi: 10.1614/WS-05-003R1.1

CrossRef Full Text | Google Scholar

Warwick, S. I., Xu, R., Sauder, C., and Beckie, H. J. (2008). Acetolactate synthase target-site mutations and single nucleotide polymorphism genotyping in ALS-resistant kochia (Kochia scoparia). Weed Sci. 56, 797–806. doi: 10.1614/WS-08-045.1

CrossRef Full Text | Google Scholar

Weitbrecht, K., Muller, K., and Leubner-Metzger, G. (2011). First off the mark: early seed germination. J. Exp. Bot. 62, 3289–3309. doi: 10.1093/jxb/err030

PubMed Abstract | CrossRef Full Text | Google Scholar

Xiang, Y., Nakabayashi, K., Ding, J., He, F., Bentsink, L., and Soppe, W. J. J. (2014). Reduced Dormancy5 encodes a protein phosphatase 2C that is required for seed dormancy in Arabidopsis. Plant Cell 26, 4362–4375. doi: 10.1105/tpc.114.132811

PubMed Abstract | CrossRef Full Text | Google Scholar

Yajima, W., Hall, J. C., and Kav, N. V. (2004). Proteome level differences between auxinic herbicide susceptible and resistant wild mustard (Sinapis arvensis L.). J. Agri. Food Chem. 52, 5063–5070. doi: 10.1021/jf0495284

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Sinapis arvensis, ALS inhibitor, herbicide resistance, point mutations, seed dormancy, germination, gibberellins

Citation: Topuz M, Nemli Y, Fatima T and Mattoo AK (2015) Seed dormancy is modulated in recently evolved chlorsulfuron-resistant Turkish biotypes of wild mustard (Sinapis arvensis). Front. Chem. 3:46. doi: 10.3389/fchem.2015.00046

Received: 21 May 2015; Accepted: 09 July 2015;
Published: 24 July 2015.

Edited by:

Jimmy R. Botella, University of Queensland, Australia

Reviewed by:

Kenneth Wilson, University of Saskatchewan, Canada
Anirudha R. Dixit, NASA/John F Kennedy Space Center, USA

Copyright © 2015 Topuz, Nemli, Fatima and Mattoo. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Autar K. Mattoo, Sustainable Agricultural Systems Laboratory, Henry A. Wallace Beltsville Agricultural Research Center, USDA-ARS, Building 001, Beltsville, MD 20705-2350, USA,