Stepień Łukasz, Holubec Vojtech, Chełkowski Jerzy
Institute of Plant Genetics, Polish Academy of Sciences, ul. Strzeszyńska 34, 60-479 Poznań, Poland.
J Appl Genet. 2002;43(4):423-35.
Sequence tagged site (STS) markers have been developed recently to identify resistance genes in wheat. A number of wild relatives have been used to transfer resistance genes into wheat cultivars. Accessions of wild species of Triticeae: Aegilops longissima (4), Ae. speltoides (6), Ae. tauschii (8), Ae. umbellulata (3), Ae. ventricosa (3), Triticum spelta (2), T. timopheevi (3), T. boeoticum (4) and T. monococcum (1), 34 in total, were examined using PCR-STS markers for resistance genes against Puccinia recondita f.sp. tritici (Lr) and Erysiphe graminis (Pm). Additionally, a set of cv. Thatcher near-isogenic lines conferring resistance genes Lr 1, Lr 9, Lr 10, Lr 24, Lr 28, Lr 35 and Lr 37 were examined with the same procedure. Twenty-two accessions were tested using the inoculation test for resistance to Erysiphe graminis, Puccinia recondita, P. striiformis and P. graminis. The most resistant entries were those of Aegilops speltoides and Triticum timopheevi and among T. boeoticum accession #5353. Markers of all mentioned Lr resistance genes were identified in all corresponding cv. Thatcher near-isogenic lines (except Lr 35 gene marker). The following resistance gene markers were identified in wild Triticeae accessions: Lr 1 in two accessions of Ae. tauschii and one accession of Ae. umbellulata, Lr 9 in one accession of Ae. umbellulata, Lr 10 in one accession of T. spelta, Lr 28 in 11 accessions: Ae. speltoides (4), Ae. umbellulata (2), T. spelta (2) and T. timopheevi (3), Lr 37 in 3 accessions of Ae. ventricosa, Pm 1 in all 34 accessions, Pm 2 in 28 accessions, Pm 3 in all 4 accessions of T. boeoticum, 1 accession of T. spelta and 1 of T. timopheevi, and Pm 13 in 5 out of 6 accessions of Ae. speltoides. Reliability and usefulness of STS markers is discussed.
序列标签位点(STS)标记最近已被开发出来用于鉴定小麦中的抗性基因。许多野生近缘种已被用于将抗性基因转入小麦品种。对34份小麦族野生种材料:长穗偃麦草(4份)、斯卑尔脱山羊草(6份)、节节麦(8份)、伞穗山羊草(3份)、偏凸山羊草(3份)、斯卑尔脱小麦(2份)、提莫菲维小麦(3份)、野生一粒小麦(4份)和一粒小麦(1份),使用针对叶锈菌(Lr)和白粉菌(Pm)抗性基因的PCR-STS标记进行了检测。此外,对一套携带Lr1、Lr9、Lr10、Lr24、Lr28、Lr35和Lr37抗性基因的撒切尔近等基因系也采用相同方法进行了检测。对22份材料进行了接种试验,以检测其对白粉菌、叶锈菌、条锈菌和秆锈菌的抗性。抗性最强的材料是斯卑尔脱山羊草和提莫菲维小麦的一些材料以及野生一粒小麦材料编号5353。在所有相应的撒切尔近等基因系中都鉴定出了所有上述Lr抗性基因的标记(Lr35基因标记除外)。在小麦族野生种材料中鉴定出了以下抗性基因标记:Lr1存在于2份节节麦材料和1份伞穗山羊草材料中;Lr9存在于1份伞穗山羊草材料中;Lr10存在于1份斯卑尔脱小麦材料中;Lr28存在于11份材料中:斯卑尔脱山羊草(4份)、伞穗山羊草(2份)、斯卑尔脱小麦(2份)和提莫菲维小麦(3份);Lr37存在于3份偏凸山羊草材料中;Pm1存在于所有34份材料中;Pm2存在于28份材料中;Pm3存在于所有4份野生一粒小麦材料、1份斯卑尔脱小麦材料和1份提莫菲维小麦材料中;Pm13存在于6份斯卑尔脱山羊草材料中的5份中。本文还讨论了STS标记的可靠性和实用性。