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首页> 外文期刊>Czech Journal of Genetics and Plant Breeding >A preliminary report on the identification of SSR markers for bunt ( Tilletia sp.) resistance in wheat
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A preliminary report on the identification of SSR markers for bunt ( Tilletia sp.) resistance in wheat

机译:鉴定抗小麦短打(Tilletia sp。)SSR标记的初步报告

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Common bunt and dwarf bunt, caused by Tilletia caries (DC) Tul., T. foetida (Wallr) Liro., and T.?controversa , respectively, can still cause yield and quality losses, despite the availability of effective chemical treatments. Growing resistant cultivars remains the best option for economical and environmental reasons, and is the only effective alternative in organic farming. As the durability of bunt resistance has proved to be rather poor, the pyramiding of resistance genes has been envisaged as a method of extending the life of resistance genes. Molecular markers can considerably increase the efficiency of gene pyramiding, but, because incomplete expression of both susceptibility and resistance genes makes accurate phenotyping difficult, very few markers associated with bunt resistance genes have been identified to date. This is why, at the National Agricultural Research & Development Institute Fundulea-Romania, along with the breeding program for bunt resistance, research on the possible use of molecular markers for Marker Assisted Selection (MAS) was developed. Random F5 or F4 lines from crosses between a Bt11 line or a bunt resistant line derived from a Triticale/2 × wheat, and susceptible parents, were phenotyped under artificial inoculation conditions, and were genotyped using primers for several markers. Preliminary results suggest that the Bt11 gene is located on chromosome 3B, and may be associated with marker loci Xbarc180 , Xwmc623 , Xwmc808 and Xgwm285 . The gene for bunt resistance transferred from Triticale (line F00628G34-1 – possessing a 1A/1R translocation) can make MAS possible by using 1R specific markers. Although these results are preliminary, they already prove to be useful for the diversification and pyramiding of bunt resistance genes in breeding for durability of bunt resistance.
机译:尽管有有效的化学处理方法,但由Tilletia龋(DC)Tul。,T。foetida(Wallr)Liro。和T.?conversversa分别引起的普通bun和矮bun仍可能造成产量和质量下降。出于经济和环境原因,种植抗性品种仍然是最佳选择,并且是有机农业中唯一有效的替代方法。由于已经证明了抗短打性的持久性很差,所以已经设想了抗性基因的金字塔化作为延长抗性基因寿命的方法。分子标记可以显着提高基因金字塔的效率,但是,由于易感性基因和抗性基因的不完整表达使准确的表型鉴定变得困难,因此迄今为止,几乎没有发现与短打抗性基因相关的标记。这就是为什么在罗马尼亚国家农业研究与发展研究所Fundulea-Romania,以及关于抗短打的育种计划中,开展了有关分子标记用于标记辅助选择(MAS)的可能用途的研究的原因。在人工接种下对来自Tritice / 2×小麦的Bt11品系或抗短打品系与易感亲本之间杂交的随机F 5 或F 4 品系进行表型分析条件,并使用引物对几种标记进行基因分型。初步结果表明Bt11基因位于3B染色体上,可能与标记基因座Xbarc180,Xwmc623,Xwmc808和Xgwm285有关。从黑小麦转入的短打抗性基因(品系F00628G34-1 –具有1A / 1R易位)可以通过使用1R特异性标记使MAS成为可能。尽管这些结果是初步的,但已被证明可用于在抗性持久性育种中进行抗性基因的多样化和金字塔化。

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