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水稻中一个新的精细定位的源自澳洲野生稻的QTL赋予对褐飞虱的抗性。

A new finely mapped Oryza australiensis-derived QTL in rice confers resistance to brown planthopper.

作者信息

Hu Jie, Xiao Cong, Cheng Ming-Xing, Gao Guan-Jun, Zhang Qing-Lu, He Yu-Qing

机构信息

National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.

National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, PR China.

出版信息

Gene. 2015 Apr 25;561(1):132-7. doi: 10.1016/j.gene.2015.02.026. Epub 2015 Feb 12.

Abstract

Brown planthopper (BPH) is the most destructive pest of rice in Asia. The BPH resistance in the introgression line IR65482-17-511-5-7 (IR65482-17) is derived from the wild rice species Oryza australiensis. An F2:3 population from a cross between Zhenshan 97 (ZS97) and IR65482-17 was used to map three quantitative trait loci (QTLs) for seedling resistance and feeding rate to BPH. The loci were distributed on chromosomes 2, 4 and 12. The QTL qBph4.2 on chromosome 4 had the largest effect, and contributed 36-44% of the phenotypic variance with a LOD score of 19-29. To validate the effect of qBph4.2, two near-isogenic lines (NILs) containing the qBph4.2 locus in the backgrounds of ZS97 and 9311 were developed by marker-assisted backcrossing (MABC). BPH bioassays showed that lines homozygous for the IR65482-17 allele (NIL+) of qBph4.2 tented to have significantly higher seedling resistance to BPH than those homozygous for the ZS97 or 9311 alleles (NIL-). Resistance was associated with a lower feeding rate by the insect. qBph4.2 was delimited to a ~300 kb (0.04 cM) region flanked by markers RM261 and S1, and co-segregating with XC4-27. This study will facilitate map-based cloning and marker-assisted selection of the gene, and permits further studies of gene function and resistance mechanisms in rice: BPH interaction.

摘要

褐飞虱是亚洲水稻最具毁灭性的害虫。导入系IR65482 - 17 - 511 - 5 - 7(IR65482 - 17)对褐飞虱的抗性源自野生稻物种澳洲野生稻。利用珍汕97(ZS97)与IR65482 - 17杂交的F2:3群体定位了3个水稻苗期对褐飞虱抗性及取食率的数量性状基因座(QTL)。这些基因座分布在第2、4和12号染色体上。第4号染色体上的QTL qBph4.2效应最大,贡献率为36% - 44%,LOD值为19 - 29。为验证qBph4.2的效应,通过标记辅助回交(MABC)构建了在ZS97和9311背景下含有qBph4.2基因座的两个近等基因系(NIL)。褐飞虱生物测定表明,qBph4.2的IR65482 - 17等位基因纯合的株系(NIL +)对褐飞虱的苗期抗性显著高于ZS97或9311等位基因纯合的株系(NIL -)。抗性与昆虫较低的取食率相关。qBph4.2被定位到标记RM261和S1侧翼的约300 kb(0.04 cM)区域,并与XC4 - 27共分离。本研究将有助于该基因的图位克隆和标记辅助选择,并为进一步研究水稻 - 褐飞虱互作中的基因功能和抗性机制提供便利。

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