Crops ›› 2021, Vol. 37 ›› Issue (2): 1-14.doi: 10.16035/j.issn.1001-7283.2021.02.001

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Research Progress on Wheat Improvement by Using Desirable Genes from Its Relative Species

Jia Zimiao1(), Qiu Yuliang1,2, Lin Zhishan1, Wang Ke1, Ye Xingguo1()   

  1. 1Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China
    2Institute of Cotton Research, Shanxi Agricultural University, Yuncheng 044000, Shanxi, China
  • Received:2020-12-13 Revised:2021-01-16 Online:2021-04-15 Published:2021-04-16
  • Contact: Ye Xingguo E-mail:190165494@qq.com;yexingguo@caas.cn

Abstract:

Wheat is one of the most important staple food crops all over the world. With the growing population, climate change, and people's yearning for a better life, the breeding of high-quality, high-yield, and multi-resistance wheat varieties are need to secure wheat production and industrial development. However, due to the strict and continuous manual selection by breeders to develop new wheat varieties, the wheat primary gene pool has been fully utilized. Therefore, it is essential to use the secondary gene pool of wheat relatives and introduce some desirable genes into the wheat genome from its relative species through cytogenetics, molecular marker-assisted selection, and genetic engineering in combination with traditional breeding techniques and advanced biotechnology strategies, which can break through this breeding bottleneck and develop new wheat varieties to meet the objectives of contemporary breeding. This paper briefly reviews some main related species and genera of wheat and potential characters harbored in these plants, and some key techniques and their features by which the available foreign genes can be transferred into wheat from its wild relatives by translocation. The latest research progress on the breeding modification of wheat for disease resistance, quality enhancement, growth, and development regulation were also reviewed in this paper. Besides, the existing problems and future aspects in this field were discussed to promote the mining of excellent genes in wheat relative species and the development of new varieties of wheat.

Key words: Wheat, Relative species, Foreign gene integration, Genetic improvement

Fig.1

Growth performance of several relative species of common wheat at adult stage a: Thinopyrum elongatum (Host) Nevski.; b: Secale cereale L.; c: Dasypyrum villosum L.; d: Hordeum vulgare L."

Table 1

Summary for the introgression of disease resistance genes into wheat from its alien species"

基因名称Gene 来源Source 易位染色体Translocation chromosome 参考文献Reference
白粉病抗性基因Resistance genes for powdery mildew
Pm2b 冰草[Agropyron cristatum (L.) Gaertn.] 5DS [52]
Pm4 一粒小麦(Triticum monococcum L.) 2AL [53]
Pm6 提莫非维小麦(Triticum timopheeviiZhuk.) T2BS·2GL [54]
Pm50 栽培二粒小麦(Triticum dicoccum L.) 2AL [55]
Pm51 长穗偃麦草(Thinopyrum elongatum 2BL [56]
PmCH89 中间偃麦草[Thinopyrum intermedium(Host) Beauv.] 4BL [57]
PmL962 中间偃麦草[Thinopyrum intermedium(Host) Beauv.] 2BS [58]
Pm53 拟斯卑尔脱山羊草(Aegilops speltoides Tausch) 5BL [59]
Pm55 簇毛麦(Dasypyrum villosum L.) T5AL·5VS [24]
Pm57 西尔斯山羊草(Aegilops searsiiFeldman & Kislev.) T2BS-2BL·2Ss#1L [60]
Pm58 节节麦(Aegilops tauschii Coss.) 2DS [61]
Pm62 簇毛麦(Dasypyrum villosum L.) T2BS·2VL [42]
Pm66 高大山羊草(Aegilops longissima L.) T4BL·4SLS [44]
Pm67 簇毛麦(Dasypyrum villosum L.) T1DL·1VS [43]
条锈病抗性基因Resistance genes for stripe rust
Yr35 二粒小麦(Triticum dicoccoides L.) 6BS [62]
Yr38 沙融山羊草(Aegilops sharonensisEig.) 6AL [63]
Yr50 中间偃麦草[Thinopyrum intermedium(Host) Beauv.] 4BL [64]
Yr53 圆锥小麦(Triticum turgidum L.) 2BL [65]
YrH9020a 华山新麦草(Psathrostachys huashanica Keng) 6D [66]
Yr69 长穗偃麦草(Thinopyrum elongatum 2AS [67]
YrH9017 华山新麦草(Psathrostachys huashanica Keng) 2AL [68]
YrH922 华山新麦草(Psathrostachys huashanica Keng) 3BL [69]
Yr70 小伞山羊草(Aegilops umbellulataZhuk.) 5DS [70]
Yr83 黑麦(Secale cereale L.) 6RL [71]
叶锈病抗性基因Resistance genes for leaf rust
Lr66 拟斯卑尔脱山羊草(Aegilops speltoides Tausch) 3A [72]
Lr76 小伞山羊草(Aegilops umbellulataZhuk.) 5DS [70]
LrM 马克格拉菲亚山草[Aegilops markgrafii(Greuter) Hammer] 2AS [73]
秆锈病抗性基因Resistance genes for stem rust
Sr44 中间偃麦草[Thinopyrum intermedium(Host) Beauv.] T7DS·7Ai#lS [74]
Sr46 节节麦(Aegilops tauschii Coss.) 2DS [75]
Sr47 拟斯卑尔脱山羊草(Aegilops speltoides Tausch) 2BL [76]
Sr51 西尔斯山羊草(Aegilops searsiiFeldman & Kislev.) T3AL·3SsS [77]
Sr52 簇毛麦(Dasypyrum villosum L.) T6AS·6V#3L [25]
Sr53 卵穗山羊草(Aegilops geniculata L.) T5AS·5MgL [78]
Sr59 黑麦(Secale cereale L.) T2DS·2RL [79]
赤霉病抗性基因Resistance genes for Fusarium head blight
Fhb6 日本披碱草(Elymus tsukushiensisHonda.) T1AS·1Ets#1S [50]
Fhb7 长穗偃麦草(Thinopyrum elongatum T7DS·7el2L [80]
小麦条纹花叶病抗性基因Resistance genes for wheat streak mosaic virus
Wsm3 中间偃麦草[Thinopyrum intermedium(Host) Beauv.] T7BS·7BL7S#3L [81]
小麦纹枯病抗性基因Resistance genes for wheat eyespot
Pch1 偏凸羊草(Aegilops ventricosaTausch) 7DV [82]
[1] 蔡荣. 农业化学品投入状况及其对环境的影响. 中国人口·资源与环境, 2010,20(3):107-110.
[2] Li H J, Zhou Y, Xin W L, et al. Wheat breeding in northern China:achievements and technical advances. The Crop Journal, 2019,7(6):718-729.
[3] Hao M, Zhang L Q, Ning S Z, et al. The resurgence of introgression breeding,as exemplified in wheat improvement. Frontiers in Plant Science, 2020,11:252.
[4] Zhang P, Dundas I S, McIntosh R A, et al. Wheat-Aegilops Introgressions.//Molnár-Láng M et al. (eds) Alien Introgression in Wheat. Springer International Publishing, Switzerland, 2015: 220-243.
[5] Zhou J, Ma C, Zhen S, et al. Identifcation of drought stress related proteins from 1Sl(1B) chromosome substitution line of wheat variety Chinese Spring. Botanical Studies, 2016,57:20.
[6] Deng X, Wang S L, Zhen S M, et al. Identification and molecular characterization of one novel 1Sl-encoded s-type low molecular weight glutenin B-subunit from 1Sl(1B) substitution line of wheat variety Chinese Spring (Triticum aestivum L.). Biologia, 2016,71:1212-1222.
[7] Hsam S, Lapochkina I, Zeller F. Chromosomal location of genes for resistance to powdery mildew in common wheat (Triticum aestivum L.) Gene Pm32 in a wheat-Aegilops speltoides translocation line. Euphytica, 2003,133:367-370.
[8] Jia J, Devos K, Chao S, et al. RFLP-based maps of the homoeologous group-6 chromosomes of wheat and their application in the tagging of Pm12,a powdery mildew resistance gene transferred from Aegilops speltoides to wheat. Theoretical and Applied Genetics, 1996,92(5):559-565.
[9] Petersen S, Lyerly J H, Worthington M L, et al. Mapping of powdery mildew resistance gene Pm53 introgressed from Aegilops speltoides into soft red winter wheat. Theoretical and Applied Genetics, 2015,128(2):303-312.
[10] Kuraparthy V C, Parveen D, Harcharan S K. Characterization and mapping of cryptic alien introgression from Aegilops geniculata with new leaf rust and stripe rust resistance genes Lr57 and Yr40 in wheat. Theoretical and Applied Genetics, 2007,114(8):1379-1389.
[11] Zeller F J, Kong L, Hartl L, et al. Chromosomal location of genes for resistance to powdery mildew in common wheat (Triticum aestivum L. em Thell.) 7. Gene Pm29 in line Pova. Euphytica, 2002,123(2):187-194.
[12] 李振声, 容珊, 陈漱阳, 等. 小麦远缘杂交. 北京: 科学出版社, 1985.
[13] Barkworth M E, Dewey D R. The genomic system of classification as a guide to intergeneric hybridization with the perennial Triticeae. Gene Manipulation in Plant Breeding, 1984,35(1):202.
[14] Dong Y S, Zhou R H, Xu S J, et al. Desirable characteristics in perennial Triticeae collected in China for wheat improvement. Hereditas, 1992,116:175-178.
[15] Chen J F, Lou X D, Qian C T, et al. Cucums monosomic alien addition lines:morphological,cytological,and genotypic analyses. Theoretical and Applied Genetics, 2004,108(7):1343-1348.
[16] Dvořák J, Chen K C. Phylogenetic relationships between chromosomes of wheat and chromosome 2E of Elytrigia elongata. Canadian Journal of Genetics and Cytalogy, 1984,26(2):128-132.
[17] Liu Z, Li D Y, Zhang X Y. Genetic relationships among five basic genomes St,E,A,B and D in Triticeae revealed by genomic southern and in situ hybridization. Journal of Integrative Plant Biology, 2007,49(7):1080-1086.
[18] 史娜溶, 李静静, 吴慧玉, 等. 西农979中长穗偃麦草(Thinopyrum ponticum)的遗传成分分析. 作物杂志, 2019(1):15-21.
[19] An D, Ma P, Zheng Q, et al. Development and molecular cytogenetic identification of a new wheat-rye 4R chromosome disomic addition line with resistances to powdery mildew,stripe rust and sharp eyespot. Theoretical and Applied Genetics, 2019,132(1):257-272.
[20] 孙偲, 张鹏, 张琳, 等. 华山新麦草研究进展. 分子植物育种, 2018,16(24):8199-8207.
[21] Wang R R-C, Catherine H. Morphology and cytology of interspecific hybrids of Leymus mollis. Journal of Heredity, 1984,75(6):488-492.
[22] Gradzielewska A. The genus Dasypyrum-part 2. Dasypyrum villosum-a wild species used in wheat improvement. Euphytica, 2006,152(3):441-454.
[23] Chen Q, Conner R L, Li H, et al. Expression of resistance to stripe rust,powdery mildew and the wheat curl mite in Triticum aestivum×Haynaldia villosa lines. Canadian Journal of Plant Science, 2002,2(82):451-456.
[24] Zhang R Q, Sun B X, Chen J, et al. Pm55,a developmental-stage and tissue-specific powdery mildew resistance gene introgressed from Dasypyrum villosum into common wheat. Theoretical and Applied Genetics, 2016,129(10):1975-1984.
[25] Qi L L, Pumphrey M O, Friebe B, et al. A novel robertsonian translocation event leads to transfer of a stem rust resistance gene (Sr52) effective against race Ug99 from Dasypyrum villosum into bread wheat. Theoretical and Applied Genetics, 2011,123(1):159-167.
[26] 陈新宏, 赵继新, 刘淑会, 等. 普通小麦与大麦杂交研究进展. 西北农业学报, 2005(6):38-43.
[27] 李璋, 刘翠云, 阎正录, 等. 普通小麦×栽培大麦杂种植株及其回交后代的产生和鉴定. 遗传学报, 1987(3):188-192,244.
[28] Akmr U, Shepherd K W. Substituting ability of individual barley chromosomes for wheat chromosomes. 1. Substitutions involving barley chromosomes 1,3 and 6. Plant Breeding, 2010,109(2):141-150.
[29] Zhang M Y, Zhang W, Zhu X W, et al. Partitioning and physical mapping of wheat chromosome 3B and its homoeologue 3E in Thinopyrum elongatum by inducing homoeologous recombination. Theoretical and Applied Genetics, 2020,133(4):1277-1289.
[30] Sears E R. Genetics society of Canada award of excellence lecture an induced mutant with homoeologous pairing in common wheat. Genome, 1977,19(4):585-593.
[31] Qi L L, Friebe B, Zhang P, et al. Homoeologous recombination,chromosome engineering and crop improvement. Chromosome Research, 2007,15(1):3-19.
[32] Bie T D, Cao Y P, Chen P D. Mass production of intergeneric chromosomal translocations through pollen irradiation of Triticum durum-Haynaldia villosa amphiploid. Journal of Integrative Plant Biology, 2007(11):1619-1626.
[33] Lu M J, Lu Y Q, Li H H, et al. Transferring desirable genes from Agropyron cristatum 7P chromosome into common wheat. PLoS ONE, 2016,11(7):e0159577.
[34] Wang H, Yu Z, Li G, et al. Diversified chromosome rearrangements detected in a wheat-Dasypyrum breviaristatum substitution line induced by gamma-ray irradiation. Plants, 2019,8(6):175.
[35] Dai K L, Zhao R H, Shi M M, et al. Dissection and cytological mapping of chromosome arm 4VS by the development of wheat-Haynaldia villosa structural aberration library. Theoretical and Applied Genetics, 2019,133(1):217-226.
[36] Endo T. The gametocidal chromosome as a tool for chromosome manipulation in wheat. Chromosome Research, 2007,15:67-75.
[37] Li J, Xu X, Xu P, et al. Inducing chromosome translocation and deletions by Chinese Spring-Aegilops 2C disomic addition×Chinese Spring-Elytriga 5E disomic addition. Acta Genetica Sinica, 2003,30(4):345-349.
[38] 胡文静, 张勇, 陆成彬, 等. 小麦品种扬麦16赤霉病抗扩展QTL定位及分析. 作物学报, 2020,46(2):157-165.
[39] Zeller F J, Hsam S L. Chromosomal location of a gene suppressing powdery mildew resistance genes Pm8 and Pm17 in common wheat (Triticum aestivum L. em. Thell.). Theoretical and Applied Genetics, 1996,93(1):38-40.
[40] Hsam S L K, Zeller F J. Evidence of allelism between genes Pm8 and Pm17 and chromosomal location of powdery mildew and leaf rust resistance genes in the common wheat cultivar ‘Amigo’. Plant Breeding, 1997,166(2):119-120.
[41] Chen P D, Qi L L, Zhou B, et al. Development and molecular cytogenetic analysis of wheat-Haynaldia villosa 6VS/6AL translocation lines specifying resistance to powdery mildew. Theoretical and Applied Genetics, 1995,91(6):1125-1128.
[42] Zhang R Q, Fan Y L, Kong L N, et al. Pm62,an adult-plant powdery mildew resistance gene introgressed from Dasypyrum villosum chromosome arm 2VL into wheat. Theoretical and Applied Genetics, 2018,131(12):2613-2620.
[43] Zhang R Q, Xiong C X, Mu H Q, et al. Pm67,a new powdery mildew resistance gene transferred from Dasypyrum villosum chromosome 1V to common wheat(Triticum aestivum L.). The Crop Journal, 2020, https://doi.org/10.1016/j.cj.2020.09.012.
[44] Li H H, Dong Z J, Ma C, et al. A spontaneous wheat-Aegilops longissima translocation carrying Pm66 confers resistance to powdery mildew. Theoretical and Applied Genetics, 2020,133(4):1149-1159.
[45] Marais F, Marais A, Mccallum B, et al. Transfer of leaf rust and stripe rust resistance genes Lr62 and Yr42 from Aegilops neglecta Req. ex Bertol. to common wheat. Crop Science, 2009,49(3):871-879.
[46] 陈漱阳, 侯文胜, 张安静, 等. 普通小麦-华山新麦草异附加系的选育及细胞遗传学研究. 遗传学报, 1996,23(6):447-452,488.
[47] 傅杰, 王美南, 赵继新, 等. 抗全蚀病小麦-华山新麦草中间材料H8911的细胞遗传学研究与利用. 西北植物学报, 2003,23(12):2157-2162.
[48] Kang H, Wang Y, Fedak G, et al. Introgression of chromosome 3Ns from Psathyrostachys huashanica into wheat specifying resistance to stripe rust. PLoS ONE, 2011,6(7):e21802.
[49] Kang H Y, Zhang Z J, Xu L L, et al. Characterization of wheat-Psathyrostachys huashanica small segment translocation line with enhanced kernels per spike and stripe rust resistance. Genome, 2016,59(4):1.
[50] Cainong J C, Bockus W W, Feng Y G, et al. Chromosome engineering,mapping,and transferring of resistance to Fusarium head blight disease from Elymus tsukushiensis into wheat. Theoretical and Applied Genetics, 2015,128(6):1019-1027.
[51] Wang H W, Sun S, Ge W Y, et al. Horizontal gene transfer of Fhb7 from fungus underlies Fusarium head blight resistance in wheat. Science, 2020,368(6493):5435.
[52] Ma P T, Xu H X, Xu Y F, et al. Molecular mapping of a new powdery mildew resistance gene Pm2b in Chinese breeding line KM2939. Theoretical and Applied Genetics, 2015,128(4):613-622.
[53] Schmolke M, Mohler V, Hartl L, et al. A new powdery mildew resistance allele at the Pm4 wheat locus transferred from einkorn (Triticum monococcum). Molecular Breeding, 2012,29(2):449-456.
[54] Wan W T, Xiao J, Li M L, et al. Fine mapping of wheat powdery mildew resistance gene Pm6 using 2B/2G homoeologous recombinants induced by the ph1b mutant. Theoretical and Applied Genetics, 2020,133(4):1265-1275.
[55] Mohler V, Bauer C, Schweizer G. Pm50:a new powdery mildew resistance gene in common wheat derived from cultivated emmer. Journal of Applied Genetics, 2013,54(3):259-263.
[56] Zhan H X, Li G R, Zhang X J, et al. Chromosomal location and comparative genomics analysis of powdery mildew resistance gene Pm51 in a putative wheat-Thinopyrum ponticum introgression line. PLoS ONE, 2014,9(11):e113455.
[57] Hou L Y, Zhang X J, Li X, et al. Mapping of powdery mildew resistance gene pmCH89 in a putative wheat-Thinopyrum intermedium introgression line. International Journal of Molecular Sciences, 2015,16(8):17231-17244.
[58] Shen X K, Ma L X, Zhong S F, et al. Identification and genetic mapping of the putative Thinopyrum intermedium derived dominant powdery mildew resistance gene PmL962 on wheat chromosome arm 2BS. Theoretical and Applied Genetics, 2015,128(3):517-528.
[59] Petersen S, Lyerly J H, Worthington M L, et al. Mapping of powdery mildew resistance gene Pm53 introgressed from Aegilops speltoides into soft red winter wheat. Theoretical and Applied Genetics, 2015,128(2):303-312.
[60] Liu W, Koo D H, Xia Q, et al. Homoeologous recombination-based transfer and molecular cytogenetic mapping of powdery mildew-resistant gene Pm57 from Aegilops searsii into wheat. Theoretical and Applied Genetics, 2017,130(4):841-848.
[61] Wiersma A T, Pulman J A, Brown L K, et al. Identification of Pm58 from Aegilops tauschii. Theoretical and Applied Genetics, 2017,130(6):1123-1133.
[62] Dadkhodaie N A, Karaoglou H. Mapping genes Lr53 and Yr35 on the short arm of chromosome 6B of common wheat with microsatellite markers and studies of their association with Lr36. Theoretical and Applied Genetics, 2011,122(3):479-487.
[63] Marais G F, Badenhorst P E, Eksteen A, et al. Reduction of Aegilops sharonensis chromatin associated with resistance genes Lr56 and Yr38 in wheat. Euphytica, 2010,171(1):15-22.
[64] Liu J, Chang Z J, Zhang X J, et al. Putative Thinopyrum intermedium-derived stripe rust resistance gene Yr50 maps on wheat chromosome arm 4BL. Theoretical and Applied Genetics, 2013,126(1):265-274.
[65] Xu L S, Wang M N, Cheng P, et al. Molecular mapping of Yr53,a new gene for stripe rust resistance in durum wheat accession PI 480148 and its transfer to common wheat. Theoretical and Applied Genetics, 2013,126(2):523-533.
[66] Liu Z G, Yao W Y, Shen X X, et al. Molecular mapping of a stripe rust resistance gene YrH9020a transferred from Psathyrostachys huashanica Keng on wheat chromosome 6D. Journal of Integrative Agriculture, 2014,13(12):2577-2583.
[67] Hou L Y, Jia J Q, Zhang X J, et al. Molecular mapping of the stripe rust resistance gene Yr69 on wheat chromosome 2AS. Plant Disease, 2015,100(8):1717-1724.
[68] Ma D F, Hou L, Sun C, et al. Molecular mapping of stripe rust resistance gene YrH9017 in wheat-Psathyrostachys huashanica introgression line H9017-14-16-5-3. Journal of Integrative Agriculture, 2019,18(1):108-114.
[69] Fang Z W, Sun C, Lu T, et al. Molecular mapping of stripe rust resistance gene YrH922 in a derivative of wheat (Triticum aestivum)-Psathyrostachys huashanica. Crop and Pasture Science, 2019,70(11):939-945.
[70] Bansal M, Adamski N M, Toor P I, et al. Aegilops umbellulata introgression carrying leaf rust and stripe rust resistance genes Lr76 and Yr70 located to 9.47-Mb region on 5DS telomeric end through a combination of chromosome sorting and sequencing. Theoretical and Applied Genetics, 2020,133(3):903-915.
[71] Li J B, Dundas I, Dong C M, et al. Identification and characterization of a new stripe rust resistance gene Yr83 on rye chromosome 6R in wheat. Theoretical and Applied Genetics, 2020,133(4):1095-1107.
[72] Marais G F, Bekker T A, Eksteen A, et al. Attempts to remove gametocidal genes co-transferred to common wheat with rust resistance from Aegilops speltoides. Euphytica, 2010,171(1):71-85.
[73] Rani K, Raghu B R, Jha S K, et al. A novel leaf rust resistance gene introgressed from Aegilops markgrafii maps on chromosome arm 2AS of wheat. Theoretical and Applied Genetics, 2020,133(9):2685-2694.
[74] Liu W, Danilova T V, Rouse M N, et al. Development and characterization of a compensating wheat-Thinopyrum intermedium robertsonian translocation with Sr44 resistance to stem rust (Ug99). Theoretical and Applied Genetics, 2013,126(5):1167-1177.
[75] Yu G T, Qi J. Identification and mapping of Sr46 from Aegilops tauschii accession CIae 25 conferring resistance to race TTKSK (Ug99) of wheat stem rust pathogen. Theoretical and Applied Genetics, 2015,128(3):431-443.
[76] Yu G, Klindworth D L, Friesen T L, et al. Development of a diagnostic co-dominant marker for stem rust resistance gene Sr47 introgressed from Aegilops speltoides into durum wheat. Theoretical and Applied Genetics, 2015,128(12):2367-2374.
[77] Liu W, Jin Y, Rouse M, et al. Development and characterization of wheat-Ae. searsii Robertsonian translocations and a recombinant chromosome conferring resistance to stem rust. Theoretical and Applied Genetics, 2011,122(8):1537-1545.
[78] Liu W, Rouse M, Friebe B, et al. Discovery and molecular mapping of a new gene conferring resistance to stem rust,Sr53,derived from Aegilops geniculata and characterization of spontaneous translocation stocks with reduced alien chromatin. Chromosome Research, 2011,19(5):669-682.
[79] Rahmatov M, Rouse M N, Nirmala J, et al. A new 2DS•2RL Robertsonian translocation transfers stem rust resistance gene Sr59 into wheat. Theoretical and Applied Genetics, 2016,129(7):1383-1392.
[80] Guo J, Zhang X L, Hou Y L, et al. High-density mapping of the major FHB resistance gene Fhb7 derived from Thinopyrum ponticum and its pyramiding with Fhb1 by marker-assisted selection. Theoretical and Applied Genetics, 2015,128(11):2301-2316.
[81] Danilova T V, Zhang G R, Liu W X, et al. Homoeologous recombination-based transfer and molecular cytogenetic mapping of a wheat streak mosaic virus and Triticum mosaic virus resistance gene Wsm3 from Thinopyrum intermedium to wheat. Theoretical and Applied Genetics, 2016,130(3):1-8.
[82] Pasquariello M, Berry S, Burt C, et al. Yield reduction historically associated with the Aegilops ventricosa 7DV introgression is genetically and physically distinct from the eyespot resistance gene Pch1. Theoretical and Applied Genetics, 2020,133(3):707-717.
[83] 汪晓璐, 韩冉, 宫文萍, 等. 外源染色体导入对小麦主要农艺性状的影响. 植物遗传资源学报, 2020,21(4):834-845.
[84] 何中虎, 夏先春, 陈新民, 等. 中国小麦育种进展与展望. 作物学报, 2011,37(2):202-215.
[85] 周阳, 何中虎, 张改生, 等. 1BL/1RS易位系在我国小麦育种中的应用. 作物学报, 2004,30(6):531-535.
[86] Zhou Y, He Z H, Sui X X, et al. Genetic improvement of grain yield and associated traits in the northern China winter wheat region from 1960 to 2000. Crop Science, 2007,47:245-253.
[87] 李万隆, 李振, 穆素. 小麦品种小偃6号染色体结构变异的细胞学研究. 遗传学报, 1990(6):430-437, 493-495.
[88] Zhang J, Zhang J P, Liu W H, et al. Introgression of Agropyron cristatum 6P chromosome segment into common wheat for enhanced thousand-grain weight and spike length. Theoretical and Applied Genetics, 2015,128(9):1827-1837.
[89] Zhang J, Zhang J P, Liu W H, et al. An intercalary translocation from Agropyron cristatum 6P chromosome into common wheat confers enhanced kernel number per spike. Planta, 2016,244(4):853-864.
[90] Zhou S H, Zhang J P, Han H M, et al. Full-length transcriptome sequences of Agropyron cristatum facilitate the prediction of putative genes for thousand-grain weight in a wheat-A. cristatum translocation line. BMC Genomics, 2019,20(1):1025.
[91] Wang S L, Cao M, Yu Z T, et al. Molecular mechanisms of HMW glutenin subunits from 1Sl genome positively affecting wheat bread-making quality. PLoS ONE, 2013,8(4):1-15.
[92] Deng X, Wang S L, Zhen S M, et al. Identification and molecular characterization of one novel 1Sl-encoded S-type low molecular weight glutenin B-subunit from 1Sl(1B) substitution line of wheat variety Chinese Spring (Triticum aestivum L.). Biologia, 2016,71:1212-1222.
[93] Wang K Y, Lin Z S, Wang L, et al. Development of a set of PCR markers specific to Aegilops longissima chromosome arms and application in breeding a translocation line. Theoretical and Applied Genetics, 2018,131(1):13-25.
[94] Liu L Q, Luo Q L, Li H W, et al. Physical mapping of the blue-grained gene from Thinopyrum ponticum chromosome 4Ag and development of blue-grain-related molecular markers and a FISH probe based on SLAF-seq technology. Theoretical and Applied Genetics, 2018,131(11):2359-2370.
[95] Abbasi J, Xu J, Dehghani H, et al. Introgression of perennial growth habit from Lophopyrum elongatum into wheat. Theoretical and Applied Genetics, 2020,133(9):2545-2554.
[96] Zou H D, Wu Y, Liu H K, et al. Development and identification of wheat-barley 2H chromosome translocation lines carrying the Isa gene. Plant Breeding, 2012,131(1):69-74.
[97] Wang J, Liu C, Guo X R, et al. Development and genetic analysis of wheat double substitution lines carrying Hordeum vulgare 2H and Thinopyrum intermedium 2Ai#2 chromosomes. The Crop Journal, 2019,7(2):163-175.
[98] Joshi G P, Endo T R, Nasuda S. PCR and sequence analysis of barley chromosome 2H subjected to the gametocidal action of chromosome 2C. Theoretical and Applied Genetics, 2013,126(9):2381-2390.
[99] Peleg Z, Saranga Y, Krugman T, et al. Allelic diversity associated with aridity gradient in wild emmer wheat populations. Plant, Cell and Environment, 2008,31(1):39-49.
[100] Lucas S, Dogan E, Budak H. TMPIT1 from wild emmer wheat:first characterisation of a stress-inducible integral membrane protein. Gene, 2011,483(1):22-28.
[101] Stuart L, Durmaz E, Akpınar B A, et al. The drought response displayed by a DRE-binding protein from Triticum dicoccoides. Plant Physiology and Biochemistry, 2011,49(3):346-351.
[102] Kuzuoglu-Ozturk D, Yalcinkaya O C, Akpinar B A, et al. Autophagy-related gene,TdAtg8,in wild emmer wheat plays a role in drought and osmotic stress response. Planta, 2012,236(4):1081-1092.
[103] Mohammadi R, Farshadfar E, Aghaee-Sarbarzeh M, et al. Locating QTLs controlling drought tolerance criteria in rye using disomic addition lines. Cereal Research Communications, 2003,31(3/4):257-264.
[104] Ehdaie B, Whitkus R W, Waines J G. Root biomass,water-use efficiency,and performance of wheat-rye translocations of chromosomes 1 and 2 in spring bread wheat 'Pavon'. Crop Science, 2003,43(2):710-717.
[105] 李立会, 董玉琛. 普通小麦与沙生冰草属间杂种的产生及细胞遗传学研究. 中国科学, 1990(5):492-496.
[106] Zhao R, Wang H, Xiao J, et al. Induction of 4VS chromosome recombinants using the CS ph1b mutant and mapping of the wheat yellow mosaic virus resistance gene from Haynaldia villosa. Theoretical and Applied Genetics, 2013,126(12):2921-2930.
[107] Li H, Lu M, Song L, et al. Production and identification of wheat-Agropyron cristatum 2P translocation lines. PLoS ONE, 2016,11(1):1-16.
[108] Luan Y, Wang X, Liu W, et al. Production and identification of wheat-Agropyron cristatum 6P translocation lines. Planta, 2010,232(2):501-510.
[109] Song L, Lu Y, Zhang J, et al. Physical mapping of Agropyron cristatum chromosome 6P using deletion lines in common wheat background. Theoretical and Applied Genetics, 2016,129(5):1023-1034.
[110] Mukai Y, Nakahara Y, Yamamoto M. Simultaneous discrimination of the three genomes in hexaploid wheat by multicolor fluorescence in situ hybridization using total genomic and highly repeated DNA probes. Genome, 1993,36(3):489-494.
[111] Rayburn A L, Gill B. Isolation of a D-genome specific repeated DNA sequence from Aegilops squarrosa. Plant Molecular Biology Reporter, 1986,4(2):102-109.
[112] Pedersen C, Langridge P. Identification of the entire chromosome complement of bread wheat by two-color FISH. Genome, 1997,40(5):589-593.
[113] Bedbrook J, Jones J, O'dell M, et al. A molecular description of telomeric heterochromatin in Secale species. Cell, 1980,19(2):545-560.
[114] Cao W, Hughes G, Ma H, et al. Identification of molecular markers for resistance to Septoria nodorum blotch in durum wheat. Theoretical and Applied Genetics, 2001,102(4):551-554.
[115] 代程, 张锦鹏, 武晓阳, 等. 小麦背景下冰草6P染色体特异EST标记的开发. 作物学报, 2012,38(10):1791-1801.
[116] 陈士强, 秦树文, 黄泽峰, 等. 基于SLAF-seq技术开发长穗偃麦草染色体特异分子标记. 作物学报, 2013,39(4):727-734.
[117] Li S J, Lin Z S, Liu C, et al. Development and comparative genomic mapping of Dasypyrum villosum 6V#4S-specific PCR markers using transcriptome data. Theoretical and Applied Genetics, 2017,130(10):2057-2068.
[118] Bhullar R, Nagarajan R, Bennypaul H, et al. Silencing of a metaphase I-specific gene results in a phenotype similar to that of the Pairing homeologous 1 (Ph1) gene mutations. Proceedings of the National Academy of Sciences of the United States of America, 2014,111(39):14187-14192.
[119] Rey M, Martín A C, Higgins J, et al. Exploiting the ZIP4 homologue within the wheat Ph1 locus has identified two lines exhibiting homoeologous crossover in wheat-wild relative hybrids. Molecular Breeding, 2017,37(8):95.
[120] 叶兴国, 陈明, 杜丽璞, 等. 小麦转基因方法及其评述. 遗传, 2011,33(5):422-430.
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