Original Research ARTICLE
Maternal Haploids Are Preferentially Induced by CENH3-tailswap Transgenic Complementation in Maize
- Biology Research, Syngenta Crop Protection, Research Triangle Park, Durham, NC, USA
Doubled haploid plants are invaluable breeding tools but many crop species are recalcitrant to available haploid induction techniques. To test if haploid inducer lines can be engineered into crops, CENH3−∕− and CENH3:RNAi lines were complemented by AcGREEN-tailswap-CENH3 or AcGREEN-CENH3 transgenes. Haploid induction rates were determined following testcrosses to wild-type plants after independently controlling for inducer parent sex and transgene zygosity. CENH3 fusion proteins were localized to centromeres and did not cause vegetative defects or male sterility. CENH3:RNAi lines did not demonstrate consistent knockdown and rarely produced haploids. In contrast, many of the complemented CENH3−∕− lines produced haploids at low frequencies. The rate of gynogenic haploid induction reached a maximum of 3.6% in several hemizygous individuals when backcrossed as males. These results demonstrate that CENH3-tailswap transgenes can be used to engineer in vivo haploid induction systems into maize plants.
Doubled haploid (DH) generations facilitate production of pure homozygous seed in one generation, enabling breeders to bypass the seven or eight seasons of self-pollination that are normally required to produce inbred germplasm (Wêdzony et al., 2009). DH plants offer a shortcut to complete genome homozygosity, and they are valuable tools for trait introgression, QTL mapping, and direct cytoplasmic conversions (Chang and Coe, 2009). The DH process is initiated with the induction of haploid (1N) plants. Haploid plants are typically sterile because meiotic success requires homologous chromosome pairing. For haploids to set seed, floral cell lineages must undergo doubling (DNA replication without mitosis), which can be induced via treatment with a microtubule polymerization inhibitor such as colchicine. Doubled haploid cell lineages have two identical copies of a single genome, and self-pollinating DH plants set 100% inbred seed. While many crops in the cereals, brassicas and cucurbits are bred through DH generations, several important crop species remain recalcitrant to standard haploid induction techniques (Kasha and Maluszynski, 2003).
Haploid plants are typically induced in vitro via gametophytic embryogenesis or in vivo through haploid induction (HI) crosses.In the former, anthers, microspores or ovaries are cultured into pro-embryos that spontaneously develop into doubled haploid plants (Barnabás et al., 1999; Seguı'-Simarro and Nuez, 2007). In the latter, a line of interest is crossed to a haploid inducer line, and after fertilization, a fraction of the embryos develop as haploids containing only the genome of interest (Qiu et al., 2014). While the mechanism varies in different systems, the process often involves elimination of the inducer genome in early embryogenesis (Zhang et al., 2008).
The developmental genetics underlying genome elimination is not well-understood. The process was recently engineered via heterologous complementation of CENTROMERIC HISTONE3 (CENH3) with tail-altered versions of the same gene (Ravi and Chan, 2010). CENH3 is the centromere-specific variant of HISTONE3 (H3) and is required for kinetochore nucleation and spindle attachment in mitosis and meiosis. CENH3 is composed of two domains. The DNA-binding histone fold domain (HFD) is conserved across higher eukaryotes and is very similar to the same domain in H3. In contrast, the N-terminal tail domain varies widely among closely related species and has been hypothesized to be involved in speciation (Maheshwari et al., 2015). Ravi and Chan produced Arabidopsis cenh3/cenh3 lines complemented by CENH3-tailswap transgenes in which the N-terminal tail was swapped with the shorter H3 tail. These lines produced little pollen and set predominantly diploid seed after self-pollination.
However, when these lines were backcrossed by wild-type pollen, the female tailswap chromosomes were frequently lost post-fertilization, resulting in the production of ~30% androgenic haploids (in which the male genome was maintained while the female genome was lost), as well as many aneuploids in which the female genome was partially lost. The authors reasoned that centromeres constructed with tail-altered CENH3 proteins function normally until they are forced to compete with wild-type centromeres for centromere loading with kinetochore components in the hybrid zygote and early embryo. This causes reduced spindle attachment of the inducer genome, leading to elimination of those chromosomes via fragmentation, and micronuclei formation during mitosis. It has remained unclear why haploids were found more frequently when the altered CENH3 was on the female side of the backcross (~30%) than the male (4%), but incomplete penetrance is a common feature of genome elimination in other induction systems (Zhao et al., 2013).
Worldwide the maize hybrid seed market is supported by industrial DH pipelines that utilize intra-specific in vivo haploid inducer lines derived from Stock6 (Coe, 1959). In contrast to CENH3-based induction, Stock6 and its derivative lines only act as haploid inducers when they are used as the male parent in the induction cross (i.e., induced gynogenesis) (Xu et al., 2013). As with CENH3-based induction, it is thought that the male inducer chromosomes are eliminated post-fertilization in early embryo development. Maize DH production is characterized by high rates of embryo abortion and low seed set, likely due to instability of the inducer chromosomes during the development of the embryo and endosperm (Zhang et al., 2008). These inefficiencies increase DH production costs and limit the rate at which new inbred lines can be developed.
In the present study ZmCENH3 knock-down and knock-out lines were complemented with tail-altered ZmCENH3 transgenes, and haploid induction rates (HIR) were measured following reciprocal backcrosses to wild-type. Twelve CENH3 complementation strategies were tested by independently controlling for parent sex and transgene zygosity in the context of two tail sequences. While many of the strategies led to modest levels of HI, one had a strong effect, which may provide guidance for future endeavors in CENH3 engineering.
Two approaches were undertaken to eliminate native CENH3 - a native gene knockout method, and an RNAi method. In the latter, a dsRNA hairpin targeting the native CENH3 hyper-variable tail sequence was added to the AcGREEN-CENH3 and AcGREEN-tailswap-CENH3 transgenic constructs. To avoid RNAi targeting, the CENH3 transgene tail sequences were codon-altered. T0 transformants made in the NP2222 background were self-pollinated, and homozygous T1 progeny were forwarded to haploid induction tests. A total of 21 individuals from 10 events were tested for haploid induction via reciprocal backcrosses to NP2222. Some individuals were backcrossed multiple times onto several NP2222 ears. In total, 50 ears were generated and over 5000 embryos were evaluated via transgene PCR assays to assess ploidy status.
In the native gene knockout method, the AcGREEN-CENH3 and AcGREEN-tailswap-CENH3 transgenes were introduced into a background heterozygous for a UniformMu allele obtained from the maize Co-op (UFMu-01386, http://www.maizegdb.org/uniformmu). In this allele the transposon insertion is in the first exon of the ZmCENH3 gene (GRMZM2G158526). Though other grass species have two versions of CENH3, there appears to be only one in maize (Zhong et al., 2002), an assertion supported by the fact that this cenh3 transposon insertion allele is homozygous lethal. To generate homozygous lines complemented by one of the CENH3 transgenes, the cenh3 allele was introgressed from the W22 donor line into NP2222 via three backcrosses. Then, CENH3/cenh3 heterozygous BC3 plants were crossed to transgenic T0 plants carrying one of the two tail-altered versions of CENH3. The F1 progeny were self-pollinated and homozygous cenh3/cenh3 F2 plants were selected for reproductive evaluations. All homozygous mutant plants were complemented by at least one copy of a transgene, and hemizygous and homozygous individuals were independently evaluated. A total of 10 events were tested for haploid induction via reciprocal crosses to NP2222. Several individuals were backcrossed as a male to several NP2222 ears. In total, 203 backcrossed ears were generated and nearly 17,000 embryos were extracted and tested for ploidy status. As control, several CENH3 wild-type (+/+) plants with two copies of the AcGREEN-tailswap-CENH3 transgene were tested for haploid induction rates. A total of 3072 control progeny were tested.
Two CENH3 fusion transgenes were synthesized: AcGREEN-CENH3 and AcGREEN-tailswap-CENH3. For the AcGREEN-tailswap-CENH3 transgene, the CENH3 hyper-variable tail sequence was replaced with the maize H3 tail sequence (N-MARTKHQAVRKTAEKPKKKLQF ERSGGASTSATPERAAGTGGRAASGGDSVKKTKPRHRW-). For the AcGREEN-CENH3 transgene, the CENH3 hyper-variable tail sequence was codon-altered to avoid RNAi knockdown, but the amino acid sequence was not changed. The partial CENH3 sequence targeted by RNAi was (5′-ctcggc gacgccggaaagggctgctgggaccgggggaagagcggcgtctggaggtgactcagt taagaagacgaaaccacgccaccgctggcg gcca-3′). Twenty-three out of thirty-two codons in the RNAi-relevant sequence of AcGREEN-tailswap-CENH3 were altered at the degenerate third position. Both cassettes were driven by the native ZmCENH3 promoter, and the Clontech (http://www.clontech.com) fluorophore AcGFP1 (which we call AcGREEN) was fused to the N-terminus of both CENH3 versions to establish transgenic protein localization to centromeres. For each of the two transgenes, one construct was made such that the T-DNA insert would consist of only the native promoter and the CENH3 fusion transgene, and a second binary construct was made containing the transgene plus the RNAi hairpin designed to knock down native CENH3. The RNAi hairpin was driven by an ubiquitin promoter. The selectable marker was PMI (phosphomannose isomerase) and it was driven by the maize ubiquitin promoter for selection on mannose (Negrotto et al., 2000). The four constructs were transformed into Syngenta's standard transformable inbred line NP2222 using Agrobacterium tumefaciens callus co-culture, and at least eight single copy events each were sent to the greenhouse, grown to maturity, and self-pollinated. At least five events for each construct were selected at random for further evaluation.
Homozygous transgene positive T1 plants were sampled to determine if the CENH3 transgenes were expressing and localizing properly. In at least two individuals from each of two events for each of the four constructs, samples were taken from the scutellum, lateral roots, and meiotic-staged anthers, fixed in 100% ethanol, and stained with propidium iodide (PI) using established techniques (Kelliher and Walbot, 2011). Anthers were then sectioned or imaged directly on a Zeiss laser scanning microscope (LSM 710). The AcGREEN fluorophore was visualized at 488 nm and the emission spectra was collected at 520–550 nm, while PI was excited at 560 nm and the emission spectra was collected at 600–650 nm. Images were captured using an AxioCam MRc camera and processed in ZEN 2011 image analysis software.
Meiotic staged anthers were sampled from T1 homozygous CENH3:RNAi plants to measure transcript knockdown by qRT-PCR. Prior work had established that anthers about 2.0 mm long contain hundreds of reproductive cells in meiosis (Kelliher and Walbot, 2011). Three lower floret anthers at this stage were dissected from central rachis and side branch spikelets about 2 days prior to tassel emergence from the whorl. Samples were taken in quadruplicate and transcript abundance was measured using a quantitative reverse transcriptase PCR (qRT-PCR) reaction with primers specific to the native CENH3 allele, 5′-GCGACGCCGGAAAGG-3′ and 5′-TGGCGTGGTTTCGTCTTCTTA-3′. Transcript abundance was compared to an endogenous control to standardize for starting cDNA amounts.
In both the knockout and RNAi strategies, selected lines were evaluated for reproductive fitness and reciprocally backcrossed to NP2222 for haploid induction tests. Fourteen to seventeen days after pollination, ears were harvested and viable and aborted kernels were counted. In most cases, 84 embryos were then extracted (although in a few cases, 168 embryos were extracted). After extraction, embryos were placed on solid media and allowed to germinate a rudimentary shoot during 3–7 days incubations in the dark (Supplementary Figure 1A). The root and lower part of the scutellum and embryo proper were then sampled (Supplementary Figure 1B) and tested for ploidy via PCR assay, while the remaining tissues (scutellum, embryo, and shoot) were stored at –80°C for ploidy confirmation via Flow Cytometry (ploidy analysis). Putative haploids were identified by PCR reactions that detected the transgenes and/or the cenh3 allele. For the knockout strategy, diploids were identified as having one copy of the cenh3 allele, while putative haploids were identified as having zero copies of the cenh3 allele (because the inducer genome is lost during haploid induction). For the RNAi strategy, diploids were identified by having one copy of the transgene, while putative haploids were identified by having zero copies of the transgene. Because aneuploidy or pollen contamination could easily lead to false scoring using these methods, all putative haploids were tested by Flow Cytometry on a Partec Ploidy Analyzer with UV lamp to detect DAPI stained, extracted nuclei. Samples were sliced using a razor blade for 30 s, extracted for 1 min in nuclei extraction buffer, and incubated for 5 min in DAPI stain. The gain was set at 525, the speed was set at 4 ul/sec, and the sample concentration was established to be 2000–3000 cells/mL. The limits used to categorize ploidy status were: Haploid, 1st peak 90–110, 2nd peak 180–220; Aneuploid, 1st peak 110–190, 2nd peak 220–380; Diploid, 1st peak 190–210, 2nd peak 380–420.
Haploid induction rates were compared to the background rate in maize by a two-tailed Z-test for comparing two proportions. The background rate was established to be 0.065% (see Table 1). For evaluation of RNAi efficacy, relative transcript abundance for each sample was compared by Student's T-test to the average of the four control samples on the same plate.
Table 1. Haploid induction frequency determination in control (CENH3 +/+) lines complemented by two copies of the AcGREEN-tailswap-CENH3 transgene.
Two tail-altered CENH3 transgenes, AcGREEN-CENH3 and AcGREEN-tailswap-CENH3, were each tested with two native gene complementation strategies (Figure 1). In the first strategy binary vectors were constructed containing one of the two transgenes plus a dsRNA hairpin cassette designed to target the CENH3 tail in native transcripts only. In the second elimination strategy, transgenic events lacking the dsRNA hairpin were introgressed into a cenh3/cenh3 background. Figure 1 summarizes the numbers of events, individual plants, and progeny tested for each approach. In total, 20 events, 243 crosses, and 22,000 embryos were screened.
Figure 1. Experimental overview of the four CENH3 complementation strategies tested. Two native CENH3 elimination methods (top row) were paired with each of the two transgenes (left column). The number of transgenic events studied, plants crossed, and progeny screened for each strategy is shown in the four gray boxes (bottom right). In the top right corner of these boxes, the corresponding data table for that box's strategy is indicated. Not included in this diagram is the experimental design for the control data measuring the background haploid induction rate. The experimental set up for that test is described in the methods, and the data is found in Table 1.
To establish that the fusion proteins localized to centromeres, one transgene-negative and two transgene-positive T1 individuals were imaged from at least two events from each of the four constructs. In every transgene-positive sample checked, multiple cells in the scutellum (Figures 2A,B), and meiotic staged anther (Figure 2C) had several intra-nuclear AcGREEN+ spots, consistent with a centromeric localization. This pattern was not found in any of the negative control samples checked (Figure 2D), but it was found in transgene-hemizygous and -homozygous individuals, regardless of the presence or absence of the native CENH3 wild-type allele. Only ~40% of nuclei in a given tissue sample had this pattern, while the remaining nuclei did not have any fluorescent signal in the AcGREEN channel. This is consistent with the idea that CENH3 loading on centromeres is cell-cycle dependent. In most nuclei that had the signal, between 8 and 10 dots were clearly distinguished, but some nuclei had up to 20 dots, most likely due to endo-reduplication or because those cells were in the G2 phase of the cell cycle.
Figure 2. AcGREEN-tailswap-CENH3 localizes to centromeres. These images are representative of those found in all events checked from all four constructs. (A) CENH3 localization has a punctate pattern in the scutellar nuclei of a transgene-hemizygous individual from event *32A. Arrow indicates a nucleus containing several CENH3+ foci corresponding to centromeres. (B) Close up of (A). Arrow indicates one CENH3+ centromere. (C) CENH3 localizes to nuclei in the epidermal and endothecial cells of the pre-meiotic (~1.0 mm long) anther from a transgene-hemizygous individual from event *32A. Arrow indicates one epidermal cell nucleus with several discrete CENH3+ centromeres. (D) CENH3 was not observed in a transgene-null individual from event *32A. Arrow indicates one scutellar nucleus with no CENH3+ centromeres visible. PI, propidium iodide; ep, epidermal cells; en, endothecial cells.
To establish the control rate of haploid induction in our transgenic plant population, plants homozygous for wild-type CENH3 were used in induction tests. CENH3/CENH3 F2 plants homozygous for the AcGREEN-tailswap-CENH3 transgene were identified from each of four events and 37 backcrosses were made to wild-type (25 through the male, and 12 through the female). Two haploids were found among the 3072 progeny tested (Table 1). With this level of investigation, the control induction rate was thus found to be ~0.065%, which falls in the reported background range of gynogenic haploid induction (0.05–0.1%; Chang and Coe, 2009).
The impact of the dsRNA hairpin transgenic cassette on native CENH3 expression was evaluated by qRT-PCR in the T1 generation of five events for each construct. Homozygous T1 plants were compared to siblings lacking the transgenes. Meiotic staged anthers were chosen as the tissue to evaluate Cenh3 knockdown because they contain active mitosis and meiosis, both of which require CENH3. To ensure a statistically sound assessment of transcript abundance, four homozygous plants from each event were tested in triplicate. A majority of the plants exhibited only a slight down-regulation of Cenh3 mRNA compared to controls (Figures 3A,B). Fourteen individuals were significantly knocked down (p < 0.01) and had mRNA levels between 21 and 65% of the average of the controls. Ten AcGREEN-tailswap-CENH3 and nine AcGREEN-CENH3 plants with strong knockdown, and one unaffected individual from each construct, were forwarded to reproductive evaluations and haploid induction tests through reciprocal backcrosses to wild-type.
Figure 3. Cenh3 knockdown by RNAi. Five events from each RNAi construct were grown and four transgene-homozygous individuals from each were sampled to measure the extent of Cenh3 knockdown. Four transgene-negative siblings from each construct were sampled and tested for comparison (Null sib 1-4). Samples were analyzed by qRT-PCR using a primer pair specific to the CENH3 tail. The X-axis is a ratio of Cenh3 expression to the endogenous control. Individuals were tested in triplicate and error bars indicate the standard deviation in the replicates. Results are displayed in rank order with the highest relative expression at the top of each chart. (A) Native CENH3 expression levels in individuals from AcGREEN-CENH3 + CENH3:RNAi events. (B) Native Cenh3 expression levels in individuals from AcGREEN-tailswap-CENH3 + CENH3:RNAi events. In total, fourteen individuals had significant Cenh3 knockdown (*p < 0.01; **p < 0.001) and these, along with a few selected others, were forwarded to reproductive evaluations and haploid induction tests.
In the haploid induction tests of the RNAi lines complemented by AcGREEN-tailswap-CENH3, just 5 haploids were found out of 3084 embryos tested, for an average induction rate of 0.16% (Table 2), just slightly higher than the established background HIR for maize, which was 0.05–0.1% (Chang and Coe, 2009). Considering only the crosses in which the transgene was on the male side, the rate of induction was 0.24% (4/1669), which was not significantly higher than background (Z = 1.62, p > 0.05). One homozygous plant exhibited a haploid induction rate of 2.4% when outcrossed as a male (4/168 progeny were haploids). That plant (* 71A:4) also had the highest knockdown by RNAi, as the Cenh3 transcript abundance was equal to 18.4% of the average of the within-plate controls. The other haploid embryo was induced androgenically by an individual from a different event. For the RNAi line complemented by AcGREEN-CENH3, only one, female-induced haploid was found out of nearly 2000 embryos tested (Table 2).
Table 2. Haploid induction frequency determination for CENH3 RNAi lines complemented by AcGREEN-tailswap-CENH3 (top) and AcGREEN-CENH3 (bottom) transgenes.
In the CENH3 knockout strategy, AcGREEN-tailswap-CENH3 and AcGREEN-CENH3 T0 plants were crossed to a line heterozygous for cenh3, a recessive, transposon-insertion allele of CENH3 that is homozygous embryo lethal. Transgene-positive F1 plants carrying cenh3 were self-pollinated, and F2 progeny homozygous for cenh3 were tested for transgene zygosity status, as determined by T-DNA specific assays compared to endogenous controls (Supplementary Table S1). Among thousands of F2 progeny tested, all cenh3/cenh3 plants were complemented by at least one copy of a CENH3 transgene, confirming that cenh3 is homozygous lethal. Dozens of cenh3/cenh3 plants hemizygous or homozygous for one of the transgenes developed normally, indicating that the transgenes were functional and complemented the knock-out allele in planta.
To assess the HIR in CENH3 complementation lines, cenh3/cenh3 F2 individuals that were complemented with one of the two transgenes were reciprocally crossed to wild-type. Progeny were tested for ploidy status using PCR tests outlined in the Methods Section. Putative haploids were confirmed by ploidy analysis on a flow cytometer. In total, 203 crosses were made from 8 AcGREEN-tailswap-CENH3 and 2 AcGREEN-CENH3 events. Results were sorted by transgene zygosity (i.e., hemizygous or homozygous) and sex of the transgenic parent. There were clear differences in the HIR obtained depending on each of these factors (Tables 3, 4).
Table 3. Haploid induction frequency determination in CENH3−∕− lines complemented by one (top) or two (bottom) AcGREEN-CENH3 copies.
Table 4. Haploid induction frequency determination in CENH3−∕− lines complemented by one (top) or two (bottom) copies of the AcGREEN-tailswap-CENH3 transgene.
Specifically, low induction rates were found when the AcGREEN-CENH3 transgene was homozygous on both the female side of the cross (1 haploid out of 833 progeny) and the male side of the cross (one haploid out of 660 progeny) (Table 3). The HIR increased when hemizygous individuals were tested. These lines induced 3 haploids out of 1988 embryos when employed as female inducers, and 5 haploids out of 1578 embryos when used as pollen donors (0.31% HIR) (Table 3). This represents a statistically significant 4.9-fold increase over the control.
Slightly elevated induction rates were found when the AcGREEN-tailswap-CENH3 line was homozygous on either side of the induction cross (3/2330 as a female and 3/2342 as a male) (Table 4). Similarly, when this transgene was hemizygous and used as the female in the induction cross, a total of 8 out of 3991 embryos were identified as haploids, for an HIR of 0.20%, which is about three-fold above the background. When the AcGREEN-tailswap-CENH3 transgene was used as the male in the induction cross, 28 confirmed haploids were recovered out of 3252 embryos, for an average HIR of 0.86% (Table 4). This represents a statistically significant 13.2-fold increase over the control. The highest HIR on an ear was 3.6%, which was found four times in this set. One of the ears, a cross by pollen from individual *A004A:3, was photographed and showed ~11% embryo abortion (43/390 kernels) (Figure 4A). Some progeny from this ear were germinated and an example of a haploid and diploid were photographed at maturity (Figure 4B). Their ploidy status was confirmed via Flow Cytometry (Figures 4C,D).
Figure 4. CENH3-based haploid induction in maize. (A) Photograph of the ear crossed by pollen from individual * A004A:3, which exhibited a 3.6% haploid induction rate (3 haploids found out of 84 embryos). Such elevated levels of induction were always found coincident with low levels of embryo abortion (the white kernels in the photo) scattered around the ear. (B) Progeny from this ear were germinated on media, sampled, and identified by PCR as either haploid or diploid. Based on the PCR calls, a few putative haploid and diploid plants were then transplanted to soil and grown until the diploid plants were shedding pollen. Putative haploids (such as plant * A004A:3-104, right) were male and female sterile. They were also shorter and had thinner leaves than the putative diploids (such as plant * A004A:3-103, left). (C,D) Adult leaf samples were tested to confirm ploidy status. The diploid 2N peak was set at 200 units (X-axis) by adjusting the gain while running cells extracted from a known diploid plant through the flow cube. (C) The sample from the putative diploid plant *A004A:3-103 had a 2N peak at 200 units and a smaller 4N peak at 400 units. (D) The putative haploid plant *A004A:3-104 had a 2N peak at 100 units and a smaller 4N peak at 200 units. The image in (D) is representative of the histograms found for all putative haploids.
In the Arabidopsis study, a high level of aneuploidy was found among the progeny, likely a result of partial chromosome elimination during haploid induction. In contrast, all 60 of the maize haploids we identified by PCR assay were confirmed as true haploids via ploidy analysis. We also screened 96 putative diploids in the ploidy analyzer, specifically sampling them from ears that had haploid induction occurring. Of these 96 putative diploids, 95 were scored as true diploids via ploidy analysis, while one embryo was scored as an aneuploid. The aneuploid was from event * A008A, when the transgene was in a hemizygous state on the female side of the cross. Several other putative diploids sampled from the same ear were confirmed as diploids.
Doubled haploid generations allow breeders to bypass years of inbred line generation by single seed decent. For crops that do not have reliable haploid production methods, the 2010 Ravi and Chan study suggested that engineered haploid induction could be available for all crops. In an attempt to demonstrate the validity of that theory, we tested several biotechnological approaches toward engineering CENH3-based haploid induction in maize. Although, the rates of haploid induction were not overwhelming compared to industry-standard maize haploid inducer lines, which have been bred for high rates of induction (8–15%), we were able to demonstrate several instances of induction rates as high as 3.6% in some crosses. Such rates were found most frequently when the AcGREEN-tailswap-CENH3 transgene was hemizygous on the male side of the cross in the cenh3/cenh3 background. However, from individual to individual, the haploid induction rate varied widely and on average, the male, hemizygous induction crosses induced haploids at a frequency of 0.86%, which is 13.2-fold higher than background.
While this rate was much higher than the other reproductive strategies tested in this study (Table 5), it is still relatively low compared to the native Stock6 induction system (Coe, 1959). It is unclear why the hemizygous trasngenics consistently performed better than their homozygous counterparts. One reasonable conjecture is that it has to do with the abundance of the transgenic CENH3 protein in the absence of wild-type CENH3. One might imagine that the less transgenic CENH3 available, the higher the frequency of faulty centromere construction. Until now the only plant in which CENH3 alteration led to haploid induction was Arabidopsis. Delayed loading of CENH3 onto centromeres was shown to be concurrent with post-zygotic genome elimination in barley vulgare × bulbosum wide crosses (Sanei et al., 2011), but the present work represents the first example of engineered CENH3-based haploid induction in a monocotyledonous crop plant.
Table 5. Summary of haploid induction rate data following outcrosses with CENH3-altered transgenic maize lines.
There were significant differences between the outcomes of the Arabidopsis work and the present study. While more events and crosses were tested here, the highest HIR was significantly lower than in Arabidopsis (Ravi and Chan, 2010). In addition, the most frequent type of haploid induction seen in maize was gynogenetic induction, in which male inducer chromosomes are lost and female chromosomes are retained. Only rarely was the converse seen—when the female line was the inducer and the male chromosomes were retained. High male sterility limited study of CENH3-based gynogenesis in Arabidopsis, where a 3% HIR was found using male inducers, compared to 30% with female inducers (Ravi and Chan, 2010). It is not clear what accounts for the difference between the species, or if a lack of androgenetic haploidy will be a common feature for other monocotyledonous crops. There is a natural androgenetic mutation in maize called indeterminate gametophyte1 (ig1) (Evans, 2007). It would be interesting to determine if induction rates increase when CENH3-tailswap technology is tested in an ig1 background.
There are several biotechnological strategies for genetic complementation in plants. In this study we tested two methods to complement native CENH3 with the tail-altered transgenes. In the RNAi approach binary constructs were made containing both the tail-altered transgenes and a dsRNA designed to specifically knock down native Cenh3 transcript. This method offered the advantage of evaluating haploid induction rates in the T1 generation. We used meiosis-staged qRT-PCR to select homozygous T1 plants with the greatest extent of knockdown for forwarding to haploid induction tests. Unfortunately neither dsRNA construct induced consistent knock down, and overall, the RNAi strategy failed to induce haploids at a significantly higher rate than the background level. The one plant that induced haploids at a modest rate (2.4%) was also the plant with the strongest knockdown, but others with similar levels of knockdown did not induce haploids in the embryos tested. It is reasonable to infer that haploid induction rates will be low unless the native CENH3 protein product is either significantly reduced or eliminated. A multi-copy RNAi line may perform better than the single-copy line used in this study.
While the transgenic plants in this study did not induce haploids as frequently as in Arabidopsis (Ravi and Chan, 2010), neither did they produce nearly as many aneuploid embryos, nor did they experience a dramatic loss of male fertility. We consistently observed a low level of embryo abortion on ears (ranging from 1 to 12%) including many ears that had haploid progeny. As with the native maize Stock6 induction system, it is possible that kernel abortion is a product of partial or complete inducer chromosome elimination in the endosperm, which would produce a ploidy imbalance, a known source of endosperm failure. Based on these observations, it would be interesting to test in the future whether embryo rescue leads to higher haploid recovery rates.
While partial female sterility was observed on some ears, abundant pollen was produced in all events and there were no instances of partial male sterility. In Arabidopsis, high male and female sterility accompanied haploid induction, and pollen was pooled from several individuals just to make a single outcross. The low pollen load of the transgenics was later associated with the GFP tag, which caused CENH3 depletion in meiotic centromeres resulting in chromosome misalignment and the production of aneuploid microspores (Ravi et al., 2011). It is unclear why similar levels of sterility did not occur in this study, but it fits with a trend seen in other systems: Lower rates of haploid induction are associated with fewer pleiotropic reproductive defects.
One way in which the data presented here was consistent with the Arabidopsis work was that no haploids were found that retained chromosomes from the transgenic parent. Consistently, it appears that when a “wild-type” genome and a genome derived from a tail-altered CENH3 complementation line are hybridized, it is the genome derived from the altered CENH3 line that is lost, regardless of the sex of the parent. This observation, along with evolutionary studies of the CENH3 tail sequence, led Maheshwari et al. (2015) to hypothesize that CENH3 is involved in the development of centromere specific reproductive barriers during speciation. The authors tested this hypothesis with an elegant transgenic experiment, in which native AtCENH3 was complemented by orthologs from Lepidium oleraceum, Brassica napa, and Zea mays. These CENH3 complementation plants developed normally and were self-fertile, but outcrosses resulted in low rates (1–11%) of haploids, aneuploids, and other genomic rearrangements. It appears that in both monocots and dicots, genes with divergent CENH3 tail sequences are complementary in developmental contexts outside of hybridization.
Recently, the state of CENH3 technology was advanced by work showing that single nucleotide polymorphisms (SNPs) in the histone fold domain are sufficient to induce haploids in Arabidopsis (Karimi-Ashtiyani et al., 2015; Kuppu et al., 2015). Heterologous complementation was then used to show that such SNPs can cause centromere disruption in barley and sugar beet (Karimi-Ashtiyani et al., 2015), but haploid induction tests of barley TILLING alleles did not succeed, likely because knock-out mutations were only available for the β copy of CENH3 (Karimi-Ashtiyani et al., 2015), while the putatively redundant α copy was still functional.
In the present study, the events with the highest HIR produced multiple haploids in some crosses but none in others. For instance, in events * A034A and * B004A, several hemizygous F2 plants were crossed as males, and while one cross from each event produced three haploids, other crosses produced zero. Because the haploid induction tests in this study were performed on an F2 population generated by hybridization of NP2222 with a W22/NP2222 BC3 line, such variation may reflect segregation of genetic elements that modify the induction rate. In addition, the genomic context of the T-DNA insertion could contribute to event-by-event HIR variation.
TK: Experimental design, confocal analysis, crossing, qRT-PCR, embryo extraction, data analysis, manuscript writing. DS: Plant care, sampling for qRT-PCR, crossing, embryo extraction, manuscript editing. WW: Embryo PCR and analysis for determining haploid induction rates, manuscript editing. JM: Embryo PCR and analysis for determining haploid induction rates, manuscript editing. HZ: Producing and analyzing transformation events, manuscript editing. MN: Experimental design, construct design, manuscript editing. BM: Experimental design, project sponsorship, manuscript editing.
Internal (Syngenta) funding.
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.
The reviewer (Dr. Kumlehn) and handling editor declared their shared affiliation, and the handling editor states that the process nevertheless met the standards of a fair and objective review.
We would like to thank the University of California at Davis, especially the late Professor Simon W.-L. Chan, Professor Anne Britt, and Professor Luca Comai. Thank you for your elegant work, your inspiration and your guidance. We would also like to thank the Maize Co-op for providing the CENH3 mu-knockout line for this study. We would also like to thank Tara Liebler, Mark McLaughlin and Tim Strebe for plant production and plant care. We thank Kandi Cox, Chunyang Fan, and Janet Wall for plant sampling and analysis. We thank Qiudeng Que for lab space and personnel, and Ray Riley and Ian Jepson for project support. Thanks to Martha Dunn, Stacy Miles, Dale Skalla, and Billy Houghteling for licensing and IP guidance.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/article/10.3389/fpls.2016.00414
HIR, haploid induction rate (the number of haploid progeny as a proportion of total progeny in a haploid induction cross); DH, doubled haploid; HI, haploid induction; CENH3, CENTROMERIC HISTONE3; H3, HISTONE3; qRT-PCR, quantitative reverse transcriptase – polymerase chain reaction; PCR, polymerase chain reaction.
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Keywords: CENH3, centromeres, haploid induction, doubled haploids, genome elimination, mutant complementation, RNA interference
Citation: Kelliher T, Starr D, Wang W, McCuiston J, Zhong H, Nuccio ML and Martin B (2016) Maternal Haploids Are Preferentially Induced by CENH3-tailswap Transgenic Complementation in Maize. Front. Plant Sci. 7:414. doi: 10.3389/fpls.2016.00414
Received: 22 January 2016; Accepted: 17 March 2016;
Published: 31 March 2016.
Edited by:Inna Lermontova, Institute of Plant Genetics and Crop Plant Research, Germany
Copyright © 2016 Kelliher, Starr, Wang, McCuiston, Zhong, Nuccio and Martin. 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: Timothy Kelliher, email@example.com
†Present Address: Barry Martin, Cibo Technologies, Cambridge, MA, USA