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水稻第1染色体上对[具体病害名称未给出]抗性的数量性状位点[具体位点名称未给出]的精细定位。

Fine mapping of , a quantitative trait locus for resistance to , on rice chromosome 1.

作者信息

Mizobuchi Ritsuko, Sato Hiroyuki, Fukuoka Shuichi, Tsushima Seiya, Yano Masahiro

机构信息

National Institute of Agrobiological Sciences, 2-1-2 Kannondai, Tsukuba, Ibaraki 305-8602 Japan.

National Agriculture and Food Research Organization, Kyushu Okinawa Agricultural Research Center (NARO/KARC), 496 Izumi, Chikugo, Fukuoka 833-0041 Japan.

出版信息

Mol Breed. 2015;35(1):15. doi: 10.1007/s11032-015-0192-x. Epub 2015 Jan 20.

Abstract

Bacterial grain rot (BGR), caused by the bacterial pathogen , is a destructive disease of rice. At anthesis, rice panicles are attacked by the pathogen, and the infection causes unfilled or aborted grains, reducing grain yield and quality. Thus, increasing the level of BGR resistance is an important objective for rice breeding. A quantitative trait locus (QTL) on rice chromosome 1 that controls BGR resistance was previously detected in backcross inbred lines (BILs) derived from a cross between Kele, a resistant traditional lowland cultivar () that originated in India, and Hitomebore, a susceptible modern lowland cultivar () from Japan. Further genetic analyses using a BCF population derived from a cross between a resistant BIL (BCF) and Hitomebore confirmed that a QTL for BGR resistance was located on the long arm of chromosome 1. To define more precisely the chromosomal region underlying this QTL, we identified nine BCF plants in which recombination occurred near the QTL. Substitution mapping using homozygous recombinant and nonrecombinant plants demonstrated that the QTL, here designated as (), was located in a 502-kb interval defined by simple sequence repeat markers RM1216 and RM11727.

摘要

由细菌病原体引起的细菌性谷粒腐烂病(BGR)是水稻的一种毁灭性病害。在花期,水稻穗部受到病原体侵袭,感染导致谷粒空瘪或败育,从而降低粮食产量和品质。因此,提高对BGR的抗性水平是水稻育种的一个重要目标。先前在源自印度的抗性传统低地品种Kele(起源于印度)与日本的感病现代低地品种Hitomebore杂交产生的回交自交系(BILs)中,检测到水稻第1染色体上一个控制BGR抗性的数量性状位点(QTL)。使用源自抗性BIL(BCF)与Hitomebore杂交的BCF群体进行的进一步遗传分析证实,BGR抗性QTL位于第1染色体长臂上。为了更精确地界定该QTL所在的染色体区域,我们鉴定出9株在QTL附近发生重组的BCF植株。利用纯合重组植株和非重组植株进行的代换作图表明,该QTL(此处命名为 )位于由简单序列重复标记RM1216和RM11727界定的502-kb区间内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e8b/4298652/88e5cf468960/11032_2015_192_Fig1_HTML.jpg

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