Physical mapping of a new powdery mildew resistance locus from Thinopyrum ponticum chromosome 4AgS

Thinopyrum ponticum (Podp.) Barkworth and D.R. Dewey is a decaploid species that has served as an important genetic resource for improving wheat for the better part of a century. The wheat–Th. ponticum 4Ag (4D) disomic substitution line Blue 58, which was obtained following the distant hybridization between Th. ponticum and common wheat, has been stably resistant to powdery mildew under field conditions for more than 40 years. The transfer of 4Ag into the susceptible wheat cultivar Xiaoyan 81 resulted in powdery mildew resistance, indicating the alien chromosome includes the resistance locus. Irradiated Blue 58 pollen were used for the pollination of the recurrent parent Xiaoyan 81, which led to the development of four stable wheat–Th. ponticum 4Ag translocation lines with diverse alien chromosomal segments. The assessment of powdery mildew resistance showed that translocation line L1 was susceptible, but the other three translocation lines (WTT139, WTT146, and WTT323) were highly resistant. The alignment of 81 specific-locus amplified fragments to the Th. elongatum genome revealed that 4Ag originated from a group 4 chromosome. The corresponding physical positions of every 4Ag-derived fragment were determined according to a cytogenetic analysis, the amplification of specific markers, and a sequence alignment. Considering the results of the evaluation of disease resistance, the Pm locus was mapped to the 3.79–97.12 Mb region of the short arm of chromosome 4Ag. Because of its durability, this newly identified Pm locus from a group 4 chromosome of Th. ponticum may be important for breeding wheat varieties with broad-spectrum disease resistance.

Introduction Blumeria graminis f. sp. tritici (DC.) Speer (Bgt), which causes powdery mildew of wheat, is a biotrophic fungus that is distributed worldwide, but mainly in regions with dry and cool climates. In recent years, it has also spread to warmer and drier regions because of the intensive production of wheat at relatively high plant densities in irrigated fields in which nitrogen fertilizers are applied (Cowger et al., 2012;Singh et al., 2016). In China, Bgt races were initially isolated in the southwestern part of the country in the late 1970s, but they have since been detected in the eastern and northern regions (Xiao et al., 2022). Powdery mildew primarily damages wheat leaves and disrupts photosynthetic activities, ultimately leading to decreased plant growth and grain filling, with detrimental effects on wheat production (Zhang et al., 2020). From 2002 to 2020, powdery mildew annually affected an average of 7 million ha of the wheatgrowing regions in China (Xiao et al., 2022). Hence, breeding diseaseresistant wheat cultivars is critical for controlling powdery mildew.
To date, 65 permanently designated powdery mildew resistance genes (Pm1-Pm68) and dozens of provisionally named Ml genes have been identified in wheat and its relatives (McIntosh et al., 2021;Wu et al., 2021;Wu et al., 2022;Xiao et al., 2022). However, only a few resistance genes have been characterized via positional cloning and the application of emerging sequencing strategies. Most of these cloned Pm genes were derived from the secondary and tertiary gene pools of wheat, including Pm8 from Secale cereale L. (2n = 2x = 14, RR) (Hurni et al., 2013), Pm21 from Haynaldia villosa (L.) Schur [syn. Dasypyrum villosum (L.) Candargy, 2n = 2x = 14, VV] (He et al., 2018;Xing et al., 2018), Pm41 from Triticum turgidum ssp. dicoccoides (2n = 4x = 28, AABB) , and Pm60 from Triticum urartu Thum. ex Gandilyan (2n = 2x = 14, AA) (Zou et al., 2018). These genes all encode nucleotide-binding leucine-rich repeat (NLR) proteins that recognize effectors and trigger the defense response to powdery mildew. Among these genes, Pm8 and Pm21 have been exploited for wheat breeding in China. Specifically, approximately 50%-60% of the varieties cultivated in major wheat-producing regions contain Pm8 and more than 40 commercial varieties carry Pm21 (Cao et al., 2015;Xing et al., 2021). Because of the rapid evolution of new Bgt isolates, some of the existing resistance genes can no longer protect plants from disease (Lu et al., 2020). For example, Pm8, which was derived from chromosome 1RS of Petkus rye, has no protective effect against the new Bgt isolate No. 9 collected in Sichuan, China . Similarly, the extensive and long-term application of Pm21 has accelerated the evolution of Bgt races. Thus, Pm21 will eventually become useless for controlling powdery mildew caused by new Bgt strains (He et al., 2020). Therefore, new resistance loci must be identified and applied in wheat breeding programs.
As one of the important wild relatives of wheat, tall wheatgrass [Thinopyrum ponticum (Podp.) Barkworth and D.R. Dewey, 2n = 10x = 70, E e E e E b E b E x E x StStStSt or JJJJJJJ s J s J s J s ; syn. Agropyron elongatum (Host) P. Beauvois, Lophopyron ponticum (Podp.) ÁLöve, Elytrigia elongata (Host) Nevski, Elytrigia pontica (Podp.) Holub.] is reportedly highly resistant to powdery mildew (Zhang et al., 1996b;Zhang et al., 1997;Chen et al., 1998;Li and Wang, 2009). However, only Pm51 has been characterized. (Zhan et al., 2014). Briefly, Pm51 in the wheat-Th. ponticum introgression line CH7086 was putatively revealed to be derived from Th. ponticum following an evaluation of seedling resistance (all stage resistance, ASR) and was mapped to wheat chromosome 2BL on the basis of a population linkage analysis. Additionally, some Th. ponticum chromosomes and small chromosomal segments have powdery mildew resistance-related loci. For example, the wheat-Th. ponticum 1J s (1B) substitution line SN19647 and the 1J s (1D) substitution line CH10A5 express Pm genes related to disease resistance (Wang et al., 2020b;Li et al., 2021). Although Th. ponticum 1J s chromosomes are present in both lines, they were differentiated using molecular markers validation. Both substitution lines were proven to carry Th. ponticum-derived Pm genes by pedigree analysis at adult plant stage. The wheat-Th. ponticum translocation line 11-20-1 is immune to Bgt races at the seedling and adult plant stages . A cytogenetic analysis detected a T5DL·5AgS translocation in this line. Furthermore, the alien segment was associated with powdery mildew resistance following the analysis of the F 2 population derived from the cross between 11-20-1 and Yannong 19. Another wheat-Th. ponticum translocation line (WTT80), which carries a pair of TTh-1DS·1DL translocated chromosomes, is immune to Bgt isolate E09 at the seedling stage. The resistance gene(s) came from Th. ponticum according to a pedigree analysis . The wheat-Th. ponticum introgression lines SN0293-2 and SN0293-7 exhibit broad-spectrum powdery mildew resistance at the seedling and adult plant stages. Field tests of the parents suggested the Pm gene in these two lines was likely from Th. ponticum . Because Th. ponticum is a decaploid species with a complex and large genome, additional Pm genes will need to be identified and functionally annotated in future studies.
The blue-grained wheat line (Blue 58), was derived from the distant hybridization between common wheat variety Dami 953 and Th. ponticum, followed by successive backcrossing to wheat cultivars 573, Aifeng 3 and Tianxuan 15, during which wheat chromosome 4D was substituted by Th. ponticum chromosome 4Ag (Mu et al., 1986). The blue grain phenotype is caused by the accumulation of anthocyanin pigments in the aleurone layer. Wheat geneticists and breeders have used the blue grain-related gene as a marker to calculate the frequency of natural crosses, identify true hybrids, and monitor chromosomal changes (Zeven, 1991;Hucl and Matus-Cadiz, 2001;Metzger and Sebesta, 2004;Morrison et al., 2004;Zheng et al., 2006;Shen et al., 2013;Liu et al., 2018a). To determine the physical position of the gene responsible for the blue aleurone, a series of translocation lines was developed via irradiation. The blue grain-related gene was physically mapped to regions [0.71-0.80 and 0.75-0.89 relative fragment lengths (FL)] on the long arm of chromosome 4Ag (Zheng et al., 2006;Liu et al., 2018a). A cytogenetic analysis revealed that 4Ag was a recombinant chromosome. Its centromeric and pericentromeric regions were from the E-genome, whereas the distal regions of the two arms were from the St-genome (Zheng et al., 2006). In this study, we confirmed that chromosome 4Ag from Blue 58 also has a locus conferring excellent resistance to Bgt races at the adult plant stage. Furthermore, we constructed a relatively refined physical map of chromosome 4AgS and mapped the Pm locus using a series of translocation lines. The results of this study provide important insights into the Th. ponticum group 4 chromosome-derived Pm gene conferring adult plant resistance (APR). Moreover, the new translocations may be useful for wheat breeding programs.

Plant materials
Four wheat-Th. ponticum 4Ag translocation lines (L1, WTT139, WTT146, and WTT323) were developed from the cross Xiaoyan 81*2//Blue 58/Xiaoyan 81 ( Figure 1). Firstly, wheat cultivar Xiaoyan 81 was pollinated with the 60 Co g-ray-irradiated pollen of Blue 58. Then, selected translocation lines were backcrossed twice with the recurrent parent Xiaoyan 81. Finally, stable translocation lines were obtained from the self-bred seeds. One wheat-Th. ponticum 4Ag substitution line 19ZQ43 was developed from the same cross without irradiation. To further confirm the genetic locus and accelerate its utilization in wheat improvement, the alien segment of WTT146 was transferred into widely adaptable cultivar Jimai 22

Cytogenetic identification
Chromosome preparation was carried out according to Han et al. (2006Han et al. ( , 2009 with minor modifications. In brief, the seed roots with the length of 1-2 cm were collected, pretreated with N 2 O under 10 atm pressure for 2 hours and then fixed in 90% acetic acid for 8 min. The root tips were cut and digested with 2% cellulase and 1% pectinase before washed with 75% ethyl alcohol. The root tips were mashed using dissecting needle and diluted with 100% acetic acid. Finally, 10 mL mixture was dropped onto the center of a slide. The slides with good mitotic phases were used in sequential genomic in situ hybridization (GISH) and multi-color fluorescence in situ hybridization (mc-FISH).
The genomic DNA (gDNA) of Th. ponticum was labeled as a probe with Alexa Fluor-488-dUTP (green). While the gDNA of CS was used as a block. The probe and block with ratio of 1:200 were used in GISH analysis. After GISH, two repetitive probes, pAs1 (GenBank Accession number: D30736.1), isolated from Aegilops tauschii Coss. and labeled with Texas-red-5-dCTP (red), pSc119.2 (GenBank Accession number: KF719093), isolated from S. cereale and labeled with Alexa Fluor-488-dUTP (green), were used in the FISH analysis (Rayburn and Gill, 1986;McIntyre et al., 1990). After hybridization, the slides were washed in 2× Saline Sodium Citrate buffer followed by counterstain with 4, 6diamidino-2-phenylindole (DAPI). The cells with clear hybridization signals were photographed by a DP80 CCD camera attached to an Olympus BX53 and analyzed using the program CellSens Standard 1.12 (Olympus, Tokyo, Japan).
were evaluated at the booting and filling stages. Plants were grown in two consecutive seasons (2020-2021 and 2021-2022) at Changping Experiment Station, IGDB, Beijing, China and one growing season (2021)(2022) in Wenjiang, Chengdu, Sichuan, China. Wheat cultivar XueZao was planted next to the test rows as an inoculum spreader. The materials were naturally infected by powdery mildew. The infection types (ITs) were scored on a 0-4 scale according to the described by Fu et al. (2014), where 0-2 represent resistance and 3-4 represent susceptible.

Sequence alignment and molecular marker analysis
In a previous study, gDNA extracted from Blue 58, CS, and Th. ponticum was digested using HaeIII (New England Biolabs, America) and then specific fragments (400-450 bp) were selected for the specificlocus amplified fragment sequencing (SLAF-seq) analysis. The SLAFs of 4Ag were obtained following a comparison with the A-genome, Dgenome, and the SLAFs of CS and Th. ponticum. Our group developed 573 markers specific to chromosome 4Ag on the basis of these SLAFs of 4Ag (Liu et al., 2018a), of which 223 markers specific to chromosome 4AgS were used for the subsequent analysis. First, the SLAFs related to these markers were aligned with the Thinopyrum elongatum (Host) D.R. Dewey (2n = 2x = 14, EE) genome (Wang et al., 2020a) to reveal the homoeologous group that 4Ag belongs to and with the Th. ponticum genome (unpublished) to identify specific chromosome. The comparisons were completed using Bowtie2, with one mismatch accepted. The correct sequence was obtained if the physical distance between the forward and reverse SLAFs was less than 500 bp. These SLAFs were further mapped to a specific chromosome to determine their physical positions using BLAST, with an E-value cut off of 1e-5. Depending on the physical positions, some markers were selected and amplified by PCR using the Blue 58 gDNA. The amplified products were sequenced and aligned with the Th. ponticum and Th. elongatum genomes. Syntenic relationships were visualized using MapChart 2.32 (Voorrips, 2002). Finally, the chromosomal regions of four wheat-Th. ponticum translocation lines (L1, WTT139, WTT146, and WTT323) were determined according to a PCR amplification of these selected markers. The PCR amplification and detection were performed as described by Liu et al. (2018a).

Agronomic traits evaluation
In 2018-2019 and 2019-2020, the recurrent parent Xiaoyan 81 and the translocation line WTT146 were grown in triplicate on plots at Nanpi Eco-Agricultural Experimental Station, Chinese Academy of Sciences, Hebei Province, China (116.4°E, 38.0°N). The soil salinity of this station was 0.18% (m/m) according to the detection values in decades.  ). A total of 20 seeds were sown in a 2.0 m row with an inter-row spacing of 0.2 m. Field managements were carried out according to the common practices for wheat production with no irrigation at Nanpi station and adequate irrigation at Changping station during the whole growing seasons. Five plants located in the center of middle row were selected and investigated for agronomic traits at physiological maturity. The agronomic traits mainly included plant height (PH), effective tiller number (ETN), kernel number per main spike (KNMS), total kernel number (TKN), thousand-kernel weight (TKW) and yield per plant (YPP). The mean value and standard deviation were calculated using SPSS version 19.0 software (IBM, New York, USA). Significant difference was determined by the Student's t test. One-way ANOVA analysis was conducted using data processing system (Tang and Zhang, 2013).

Results
Powdery mildew APR locus from Th. ponticum chromosome 4Ag At the bolting and filling stages, Blue 58 was highly resistant to powdery mildew (IT = 1), whereas Xiaoyan 81 was susceptible to powdery mildew (IT = 4) (Figure 2A). At the seedling stage, Blue 58 and The powdery mildew resistance evaluation and cytogenetic analysis. Xiaoyan 81 were inoculated with Bgt race E09 and the resulting IT scores were 3 and 4, respectively ( Figure 2B), suggesting Blue 58 carried the Pm gene responsible for APR. To determine the origin of the resistance locus, we transferred 4Ag into the powdery mildewsusceptible cultivar Xiaoyan 81 and produced a new stable substitution line (19ZQ43) with the pedigree Xiaoyan 81*3/Blue 58. The 19ZQ43 grains were blue, similar to the Blue 58 grains. The GISH analysis indicated that 19ZQ43 had 42 chromosomes, including 40 wheat chromosomes and two alien chromosomes ( Figure 2C). The mc-FISH analysis revealed a strong pAs1 signal at the pericentromeric region of the short arm of the alien chromosomes, implying that 19ZQ43 carried a pair of 4Ag chromosomes ( Figure 2D). The evaluation of resistance showed that 19ZQ43 was resistant to powdery mildew at the adult plant stage (IT = 1) (Figure 2A). Thus, we speculated that Th. ponticum chromosome 4Ag contains an adultstage powdery mildew resistance locus.

Development, cytogenetic identification, and disease resistance evaluation of novel translocation lines
Four novel translocation lines were developed via irradiation and their chromosomal compositions were characterized (Figure 3). Among them, L1 has blue seeds, while lines WTT139, WTT146 and WTT323 have white seeds. The GISH analysis showed that L1 had 44 chromosomes, of which 42 were detected as blue chromosomes and two were detected as chromosomes with small blue distal ends and large green chromosomal segments ( Figure 4A). Hence, L1 likely contained 21 pairs of complete wheat chromosomes and one pair of wheat-Th. ponticum translocated chromosomes with large alien fragments. The mc-FISH analysis of the translocated chromosome of L1 detected a strong pAs1 signal near the centromere zone and a clear pSc119.2 signal near the terminal region of the short arm ( Figure 4B), indicating that the intercalary region of 4AgS was broken and the larger alien chromosomal segment was fused to an unknown wheat chromosomal segment to produce the novel translocated chromosome TW-4AgS·4AgL. A total of 44 chromosomes were identified in WTT139 ( Figure 4C). The mc-FISH analysis detected an obvious pAs1 band in the pericentromeric region of the alien chromosomal segment ( Figure 4D), suggesting that 4AgS was translocated to a small unknown wheat chromosomal fragment to produce the new translocated chromosome TW·4AgS. In addition, reciprocal translocations occurred between chromosomes 4B and 6D. The GISH results for WTT146 revealed 40 chromosomes with blue signals and two blue chromosomes with green signals at the distal ends of their short arms ( Figure 4E), implying that WTT146 was affected by the translocation of a small alien fragment. The mc-FISH analysis of the translocated chromosome detected clear pAs1 signals in the pericentromeric, intercalary, and terminal regions of the long arm, which was consistent with the signal pattern of chromosome 5DL ( Figure 4F). The lack of an obvious signal prevented the accurate determination of the location of the alien segment in 4Ag. Thus, a T4Ag-5DS·5DL translocation event likely occurred in WTT146. The GISH analysis of WTT323 detected 40 chromosomes with blue signals and two chromosomes with blue signals as well as small regions with green signals (Figure 4G), indicating it had 20 pairs of intact wheat chromosomes and a pair of intercalary wheat-Th. ponticum translocated chromosomes. The mc-FISH analysis detected the typical pSc119.2 bands of chromosome 5B in the terminal and intercalary regions of the short arm of the translocated chromosome ( Figure 4H), suggesting a small unknown alien segment was inserted into wheat chromosome 5B, resulting in the translocated chromosome T5BS·5BL-4Ag-5BL.
At the adult plant stage, consistent IT scores were obtained in Beijing and Sichuan. Specifically, the IT scores were recorded when the powdery mildew spores fully covered the leaves of the susceptible control Xiaoyan 81. Among the materials that were evaluated in terms of their disease symptoms, WTT139, WTT146, and WTT323 were highly resistant to powdery mildew (IT = 1), similar to their resistant parent Blue 58, whereas L1 and Xiaoyan 81 were highly susceptible (IT = 4) ( Figure 5; Table 1).

Alignment of selected 4AgS SLAF sequences
Because the powdery mildew-resistant line WTT139 only carries 4AgS, whereas the susceptible line L1 lacks part of a 4AgS segment, we speculated that the Pm locus was derived from 4AgS. In our previous study, 223 markers specific to chromosome 4AgS have been developed using SLAF-seq technology (Liu et al., 2018a). To further determine which homoeologous group 4Ag belongs to, the SLAFs related to these markers were compared with the Th. elongatum  Table 1). Therefore, 4Ag was proved to belong to homoeologous group 4 of Th. ponticum.
These 223 SLAFs were also compared with the Th. ponticum genome (unpublished) using the same parameters. The alignment results showed that 78 of the 223 SLAFs could be mapped to the Th. ponticum genome and 34 of these 78 SLAFs (43.59%; largest proportion) were located on chromosome LG34 (temporary name) (Supplementary Table 2). Thus, we identified chromosome 4Ag as chromosome LG34.

Physical mapping of the Pm locus on chromosome 4AgS
To elucidate the physical positions of the 223 specific markers, their SLAFs were mapped to chromosome LG34 using the BLAST online tool. A total of 113 SLAFs were mapped to chromosome LG34. More specifically, the forward and reverse SLAF sequences were highly similar (>90%) to LG34 sequences and SLAF sequences were separated by fewer than 500 bp (Supplementary Table 3). According to the BLAST sequence alignment results, 31 markers were selected for the PCR amplification of the Blue 58 gDNA (i.e., one marker per 5 Mb). The 31 PCR products were sequenced and then compared with the chromosome LG34 sequence. The physical positions of the 31 PCR products were close to the physical positions of their SLAFs (Supplementary Table 4). Additionally, eight of the 31 PCR products were similar to sequences on Th. elongatum chromosome 4E (sequence identities >85%) and revealed the good collinearity between Th. elongatum chromosome 4E and Th. ponticum chromosome LG34 ( Figure 7A; Supplementary Table 4). The primers for these 31 specific markers were used to amplify the gDNA of Blue 58, L1, WTT139, WTT146, WTT323, and Xiaoyan 81. These 31 markers were assigned to the following five bins according to the amplification results: 4AgS1, 4AgS2, 4AgS3, 4AgS4, and 4AgS5, which contained 9, 1, 3, 16, and 2 markers, respectively ( Figure 7B). The four translocation lines included different 4AgS chromosomal bins. Specifically, WTT139 contained all five chromosomal bins, with 0-204.69 Mb on chromosome LG34; L1 included bins 4AgS1-2 (106.20-204.69 Mb); WTT146 contained bins 4AgS4-5 (0-97.12 Mb); and WTT323 included bins 4AgS2-4 (3.79-113.72 Mb). After analyzing the IT scores and the alien segments in the four translocation lines, the Pm locus was mapped to bin 4AgS4. According to the The powdery mildew resistance responses of four translocation lines and Xiaoyan 81. physical positions of these specific markers, the Pm locus was narrowed to the 3.79-97.12 Mb region on 4AgS.

Genetic analysis of the powdery mildew resistance locus
To further determine the genetic effect of the Pm locus on 4AgS, we transferred the alien segment of WTT146 into wheat cultivar Jimai 22 to produce the novel stable translocation line J146, which was verified by the amplification of specific markers (Figure 8). The evaluation of powdery mildew resistance showed that the recurrent parent Jimai 22 was susceptible to Bgt races (IT = 3), but J146 was highly resistant (IT = 1) (Table 1). Therefore, the Pm locus of WTT146 was probably transferred into J146. These findings provided additional evidence that this Pm locus contributes to powdery mildew resistance.
The agronomic traits of L1, WTT139, WTT146 and WTT323 and its recurrent parent Xiaoyan 81 were investigated during the 2018-2022 growing seasons (Supplementary Table 5). Unfortunately, the yields of these lines were significantly lower than the recurrent parent Xiaoyan 81 except for WTT139. In order to improve their yield traits, we have transferred their alien chromosomal segments into wheat cultivar Jimai 22. The novel translocation line J146 was thus developed. The agronomic traits of J146 and its recurrent parent Jimai 22 were investigated during the 2021-2022 growing seasons (Supplementary Table 6). There were no significant differences in PH, ETN, KNMS, and YPP. In contrast, compared with Jimai 22, J146 had a significantly lower TKW (P < 0.01), but a significantly higher TKN (P < 0.01). In other words, there was no obvious linkage drag associated with the alien segment of J146, making it potentially useful for increasing the powdery mildew resistance in wheat breeding.

Discussion
Tall wheatgrass, which is one of the most important wild relatives of wheat, has been extensively used for the genetic improvement of wheat. To date, many elite cultivars derived from the distant hybridization between wheat and Th. ponticum have been approved and widely cultivated in China. For example, the high-quality and multi-resistant cultivar Xiaoyan 6 received the first prize for the National Award for Invention in 1985 (Hao et al., 2020). More than 60 cultivars have been Alignment results of 81 specific SLAFs to Th. elongatum genome using Bowtie 2.
derived from this backbone parent (Ma et al., 2018). Moreover, many essential resources, including wheat-Th. ponticum partial amphiploids [e.g. Xiaoyan series (Group of remote hybridization, 1977; Zhang et al., 1996a;Zheng et al., 2015), Agrotana (Chen et al., 1995), PWM series (Fedak et al., 2000), SS series (Oliver et al., 2006), BE-1 (Sepsi et al., 2008) and SN series (He et al., 2013;He et al., 2017;Pei et al., 2018)], addition lines [e.g. Ji791 and Ji924 (Li et al., 2003), W210, W211 and W212 (Wang and Wang, 2016), Xiaoyan 85 (Li et al., 2016) and WTA series ], substitution lines CH1113-B13 (Zhu et al., 2017), translocation lines [e.g. KS10-2 and KS24-1 (Kim et al., 1993;Friebe et al., 1996), RWG33 and RWG34 (Niu et al., 2014), SDAU1881 and SDAU1886 (Guo et al., 2015), Xiaoyan 447 (Li et al., 2016), Xiaoyan 851 (Li et al., 2019), WTT34 (Yang et al., 2021)] and introgression lines Shanrong 3 (Xia et al., 2003), have been developed via distant hybridizations and chromosome engineering. These cultivars and engineered materials have facilitated the transfer of valuable genes from Th. ponticum to wheat. Considering the restricted recombination between alien chromatin and wheat homoeologous sequences, it is difficult to narrow down the regions containing these valuable foreign genes using regular genetic techniques. Translocations due to the irradiation of pollen or the ph1b mutant that divide chromosomal regions may be used to map foreign genes. For example, in our previous study (Liu et al., 2018a), we used eight wheat-Th. ponticum 4Ag translocation lines to locate the gene responsible for the blue grain phenotype. Lin et al. (2022) used four deletion lines and two translocation lines to map the powdery mildew resistance locus in the 6PL bin (0.27-0.51) of Agropyron cristatum (L.) Gaertn. (2n = 4x = 28, PPPP). In addition, because the CS ph1b mutant can significantly increase meiotic homoeologous recombination, it has been widely used to induce translocations. Men et al. (2022) developed 12 CS-Ae. biuncialis 2M b recombinants through ph1b-induced homoeologous recombination. By combining the results of a cytogenetic analysis and an evaluation of the powdery mildew resistance of these recombinants, Pm2Mb was mapped to the 2M b L bin (0.49-0.66). For species lacking sequenced genomes, their chromosomes were not precisely characterized and only relative FLs were defined when we physically mapped a valuable gene. However, specific physical positions were determined for species with sequenced genomes. Thus, sequenced genomes accelerated the physical mapping of valuable genes, enabling them to be exploited in breeding programs. Fortunately, the genomes of Th. elongatum (Wang et al., 2020a) and Th. ponticum (unpublished) have been sequenced and assembled, in part because of the advances in the whole-genome sequencing of wild relatives of wheat. Thus, we were able to map the Pm locus to the 3.79-97.12 Mb region on the short arm of 4Ag (i.e., Th. ponticum chromosome LG34). Previous studies indicated that Th. elongatum, Th. bessarabicum, and Pseudoroegneria were probably the donor species of Th. ponticum (Muramatsu, 1990;Wang et al., 1991;Zhang et al., 1996a, Zhang et al., 1996bLiu et al., 2018b;Yang et al., 2021). In the present study, the PCR products for 31 specific markers were sequenced and compared with Th. ponticum chromosome LG34 and Th. elongatum chromosome 4E. Eight of these PCR products were similar to chromosome 4E (sequence identities exceeding 85%) and reflected the relatively high synteny between chromosomes LG34 and 4E. These results further suggest that Th. elongatum is one of the donor species of Th. ponticum. Powdery mildew is a devastating disease that can occur at all wheat growth stages. Genes conferring ASR and APR have been identified in wheat and its relatives. In general, the ASR-related genes are effective throughout the growth period and provide race-specific resistance, whereas the APR-related genes provide durable resistance at the adult plant stage and partial resistance to multiple pathogens (Roberts and Caldwell, 1970;Lin and Chen, 2007;Bai et al., 2022). Unfortunately, because the APR-related genes are very difficult to select on the basis of phenotypes, they have not been thoroughly characterized (Ren et al., 2012). The identified Pm genes conferring ASR (e.g., Pm1a and Pm5e) are easily overcome if the corresponding avirulence genes are mutated Xie et al., 2020;Hewitt et al., 2021). The APR-related genes, which are considered to be more durable than the ASR-related genes, often encode allele-specific proteins that differ from NLR proteins (Bai et al., 2022). For example, Pm38/Lr34/Yr18/Sr57 encodes ATPbinding cassette transporter (Krattinger et al., 2009), whereas Pm46/ Lr67/Yr46/Sr55 encodes hexose transporter (Moore et al., 2015). Therefore, to protect wheat plants from new Bgt strains, new Pm genes conferring APR will need to be identified and functionally characterized and ASR-related genes should be cloned and pyramided.
Among the Th. ponticum-derived Pm loci, only Pm51 was confirmed to confer ASR and mapped to wheat chromosome 2BL (Zhan et al., 2014). Additionally, Pm51 was derived from the wheat-Th. ponticum introgression line CH7086, which was obtained by crossing common wheat with the partial amphiploid Xiaoyan 7430. If CH7086 contains a compensating translocation, Pm51 may have originated from the group 2 chromosome of Th. ponticum. Furthermore, the mc-FISH analysis indicated the six pairs of alien chromosomes in Xiaoyan 7430 do not include chromosome 4Ag . Therefore, we concluded that the powdery mildew resistance locus on chromosome 4Ag differs from Pm51. Similarly, the combined analysis of the compensating translocation and the PCR products for specific markers suggests the Pm genes conferring ASR and APR from the wheat-Th. ponticum substitution lines CH10A5 and SN19647 were derived from the group 1 chromosomes (Wang et al., 2020b;Li et al., 2021). However, the Pm gene conferring ASR and APR from the wheat-Th. ponticum translocation line 11-20-1 originated from a group 5 chromosome . The Pm gene conferring ASR from the wheat-Th. ponticum translocation line WTT80 was also derived from a group 1 chromosome . According to the results of the Wheat 660K SNP array analysis and resequencing data, the adult-stage powdery mildew resistancerelated gene of SN0293-2 and SN0293-7 may have come from a group 6 chromosome . In the present study, the newly mapped APR-conferring Pm gene was revealed as the only Pm gene originating from a group 4 chromosome of Th. ponticum. This gene was derived from the wheat-Th. ponticum substitution line Blue 58, which was developed in 1976 (Mu et al., 1986). For over 40 years, this Pm gene has provided excellent resistance at the adult plant stage. Thus, it should be further explored and applied for breeding novel disease-resistant wheat lines. In addition, to exploit this APR-related Pm gene, the small alien segment in WTT146 has been transferred to the high-yielding variety Jimai 22 to obtain the novel and stable translocation line J146. The evaluation of disease resistance showed that J146 is highly resistant to powdery mildew at the adult plant stage. Notably, the assessment of agronomic traits indicated that YPP was not significantly different between J146 and its recurrent parent Jimai 22. The development of J146 may further promote the utility of this APR locus.
In summary, we developed five translocation lines carrying diverse alien segments by irradiating Blue 58 pollen. Of these lines, WTT139, WTT146, WTT323, and J146 were resistant to powdery mildew at the adult plant stage. By combining the results of our resistance evaluation, specific marker amplification, and alignment analysis, the Pm locus conferring APR was mapped to the 3.79-97.12 Mb region on the short arm of chromosome 4Ag. The identification of this powdery mildew resistance locus and its transfer into wheat cultivars by breeders may lead to the generation of novel diseaseresistant varieties suitable for commercial cultivation.

Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.

Ethics statement
The authors declare that the experiments comply with the current laws of the country in which they were performed.

Author contributions
ZL and QZ conceived the research; GY performed the experiments; GY and QZ drafted the manuscript. PD and WJ performed the sequence alignment using the genome of Th. ponticum. SF conducted adult plant stage resistance evaluation in Sichuan. HL and BL provided substantial help in preparing materials. All authors read and approved the final manuscript.

Funding
This project was supported by the National Natural Science Foundation of China (31971875) and the National Key Research and Development Program of China (2016YFD0102000).