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Fine mapping of qSTV11KAS a major QTL for rice stripe disease resistance

机译:水稻条纹病抗性的主要QTL qSTV11KAS的精细定位

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摘要

Rice stripe disease, caused by rice stripe virus (RSV), is one of the most serious diseases in temperate rice-growing areas. In the present study, we performed quantitative trait locus (QTL) analysis for RSV resistance using 98 backcross inbred lines derived from the cross between the highly resistant variety, Kasalath, and the highly susceptible variety, Nipponbare. Under artificial inoculation in the greenhouse, two QTLs for RSV resistance, designated qSTV7 and qSTV11KAS, were detected on chromosomes 7 and 11 respectively, whereas only one QTL was detected in the same location of chromosome 11 under natural inoculation in the field. The stability of qSTV11KAS was validated using 39 established chromosome segment substitution lines. Fine mapping of qSTV11KAS was carried out using 372 BC3F2:3 recombinants and 399 BC3F3:4 lines selected from 7,018 BC3F2 plants of the cross SL-234/Koshihikari. The qSTV11KAS was localized to a 39.2 kb region containing seven annotated genes. The most likely candidate gene, LOC_Os11g30910, is predicted to encode a sulfotransferase domain-containing protein. The predicted protein encoded by the Kasalath allele differs from Nipponbare by a single amino acid substitution and the deletion of two amino acids within the sulfotransferase domain. Marker-resistance association analysis revealed that the markers L104-155 bp and R48-194 bp were highly correlated with RSV resistance in the 148 landrace varieties. These results provide a basis for the cloning of qSTV11KAS, and the markers may be used for molecular breeding of RSV resistant rice varieties.Electronic supplementary materialThe online version of this article (doi:10.1007/s00122-011-1557-0) contains supplementary material, which is available to authorized users.
机译:由水稻条纹病毒(RSV)引起的水稻条纹病是温带水稻种植地区最严重的疾病之一。在本研究中,我们使用来自高抗性品种Kasalath和高度敏感品种Nipponbare之间杂交的98个回交自交系,对RSV抗性进行了定量性状基因座(QTL)分析。在温室中进行人工接种后,在7号和11号染色体上分别检测到两个RSV抗性QTL,分别称为qSTV7和qSTV11 KAS ,而在自然条件下仅在11号染色体的同一位置检测到一个QTL。现场接种。 qSTV11 KAS 的稳定性已通过39条建立的染色体片段替换系进行了验证。 qSTV11 KAS 的精细定位是使用372 BC3F2:3重组体和399 BC3F3:4品系,它们选自SL-234 / Koshihikari杂交植物的7,018 BC3F2。 qSTV11 KAS 定位于一个包含3个注释基因的39.2kb区域。预测最可能的候选基因LOC_Os11g30910编码含有磺基转移酶域的蛋白质。 Kasalath等位基因编码的预测蛋白与Nipponbare的区别在于单个氨基酸取代和磺基转移酶域内两个氨基酸的缺失。标记抗性关联分析表明,在148个地方品种中L104-155bp和R48-194bp标记与RSV抗性高度相关。这些结果为克隆qSTV11 KAS 提供了基础,该标记可用于RSV抗性水稻品种的分子育种。电子补充材料本文的在线版本(doi:10.1007 / s00122-011) -1557-0)包含补充材料,授权用户可以使用。

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