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来自“阿米戈”和“高加索”1RS.1AL染色体小麦-黑麦易位系的重组1RS上白粉病和麦二叉蚜抗性基因的连锁图谱构建

Linkage mapping of powdery mildew and greenbug resistance genes on recombinant 1RS from 'Amigo' and 'Kavkaz' wheat-rye translocations of chromosome 1RS.1AL.

作者信息

Mater Yehia, Baenziger Stephen, Gill Kulvinder, Graybosch Robert, Whitcher Lynda, Baker Cheryl, Specht James, Dweikat Ismail

机构信息

Department of Agronomy and Horticulture, University of Nebraska, Lincoln 68583, USA.

出版信息

Genome. 2004 Apr;47(2):292-8. doi: 10.1139/g03-101.

Abstract

Cultivated rye (Secale cereale L., 2n = 2x = 14, RR) is an important source of genes for insect and disease resistance in wheat (Triticum aestivum L., 2n = 6x = 42). Rye chromosome arm 1RS of S. cereale 'Kavkaz' originally found as a 1BL.1RS translocation, carries genes for disease resistance (e.g., Lr26, Sr31, Yr9, and Pm8), while 1RS of the S. cereale 'Amigo' translocation (1RSA) carries a single resistance gene for greenbug (Schizaphis graminum Rondani) biotypes B and C and also carries additional disease-resistance genes. The purpose of this research was to identify individual plants that were recombinant in the homologous region of.1AL.1RSV and 1AL.1RSA using both molecular and phenotypic markers. Secale cereale 'Nekota' (1AL.1RSA) and S. cereale 'Pavon 76' (1AL.1RSV) were mated and the F1 was backcrossed to 'Nekota' (1AL.1AS) to generate eighty BC1F2:3 families (i.e., ('Nekota' 1AL.1RSA x 'Pavon 76' 1AL.1RSV) x 'Nekota' 1AL.1AS). These families were genotyped using the secalin-gliadin grain storage protein banding pattern generated with polyacrylamide gel electrophoresis to discriminate 1AL.1AS/1AL.1RS heterozygotes from the 1AL.1RSA+V and 1AL.1AS homozygotes. Segregation of the secalin locus and PCR markers based on the R173 family of rye specific repeated DNA sequences demonstrated the presence of recombinant 1AL.1RSA+V families. Powdery mildew (Blumeria graminis) and greenbug resistance genes on the recombinant 1RSA+V arm were mapped in relation to the Sec-1 locus, 2 additional protein bands, 3 SSRs, and 13 RFLP markers. The resultant linkage map of 1RS spanned 82.4 cM with marker order and spacing showing reasonable agreement with previous maps of 1RS. Fifteen markers lie within a region of 29.7 cM next to the centromere, yet corresponded to just 36% of the overall map length. The map position of the RFLP marker probe mwg68 was 10.9 cM distal to the Sec-1 locus and 7.8 cM proximal to the powdery mildew resistance locus. The greenbug resistance gene was located 2.7 cM proximal to the Sec-1 locus.

摘要

栽培黑麦(黑麦草,2n = 2x = 14,RR)是小麦(普通小麦,2n = 6x = 42)抗虫和抗病基因的重要来源。最初发现的黑麦草“高加索”的1RS染色体臂是1BL.1RS易位,携带抗病基因(如Lr26、Sr31、Yr9和Pm8),而黑麦草“阿米戈”易位(1RSA)的1RS携带针对麦二叉蚜生物型B和C的单一抗性基因,还携带其他抗病基因。本研究的目的是使用分子和表型标记鉴定在.1AL.1RSV和1AL.1RSA同源区域重组的单株植物。将黑麦草“内科塔”(1AL.1RSA)和黑麦草“帕冯76”(1AL.1RSV)杂交,F1代与“内科塔”(1AL.1AS)回交,产生80个BC1F2:3家系(即(“内科塔”1AL.1RSAד帕冯76”1AL.1RSV)ד内科塔”1AL.1AS)。使用聚丙烯酰胺凝胶电泳产生的麦谷蛋白-醇溶蛋白谷物贮藏蛋白条带模式对这些家系进行基因分型,以区分1AL.1AS/1AL.1RS杂合子与1AL.1RSA+V和1AL.1AS纯合子。基于黑麦特异性重复DNA序列的R173家族的麦谷蛋白基因座和PCR标记的分离证明了重组1AL.1RSA+V家系的存在。将重组1RSA+V臂上的白粉病(白粉菌)和麦二叉蚜抗性基因相对于Sec-1基因座、另外2个蛋白条带、3个SSR和13个RFLP标记进行定位。由此产生的1RS连锁图谱跨度为82.4 cM,标记顺序和间距与先前的1RS图谱显示出合理的一致性。15个标记位于着丝粒旁边29.7 cM的区域内,但仅占总图长的36%。RFLP标记探针mwg68的图谱位置在Sec-1基因座远端10.9 cM处,在白粉病抗性基因座近端7.8 cM处。麦二叉蚜抗性基因位于Sec-1基因座近端2.7 cM处。

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