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通过代表性差异分析对水稻抗褐飞虱(Nilaparvata lugens Stål)的Bph1基因座进行分子标记。

Molecular tagging of the Bph1 locus for resistance to brown planthopper (Nilaparvata lugens Stål) through representational difference analysis.

作者信息

Park Dong-Soo, Song Min-Young, Park Soo-Kwon, Lee Sang-Kyu, Lee Jong-Hee, Song Song-Yi, Eun Moo Young, Hahn Tae-Ryong, Sohn Jae-Keun, Yi Gihwan, Nam Min-Hee, Jeon Jong-Seong

机构信息

Rice Division, Yeongnam Agricultural Research Institute, National Institute of Crop Science, RDA, Milyang, South Korea.

出版信息

Mol Genet Genomics. 2008 Aug;280(2):163-72. doi: 10.1007/s00438-008-0353-2. Epub 2008 Jun 14.

Abstract

During brown planthopper (BPH) feeding on rice plants, we employed a modified representational difference analysis (RDA) method to detect rare transcripts among those differentially expressed in SNBC61, a BPH resistant near-isogenic line (NIL) carrying the Bph1 resistance gene. This identified 3 RDA clones: OsBphi237, OsBphi252 and OsBphi262. DNA gel-blot analysis revealed that the loci of the RDA clones in SNBC61 corresponded to the alleles of the BPH resistant donor Samgangbyeo. Expression analysis indicated that the RDA genes were up-regulated in SNBC61 during BPH feeding. Interestingly, analysis of 64 SNBC NILs, derived from backcrosses of Samgangbyeo with a BPH susceptible Nagdongbyeo, using a cleaved amplified polymorphic sequence (CAPS) marker indicated that OsBphi252, which encodes a putative lipoxygenase (LOX), co-segregates with BPH resistance. Our results suggest that OsBphi252 is tightly linked to Bph1, and may be useful in marker-assisted selection (MAS) for resistance to BPH.

摘要

在褐飞虱取食水稻植株的过程中,我们采用改良的代表性差异分析(RDA)方法,在携带Bph1抗性基因的抗褐飞虱近等基因系(NIL)SNBC61中,检测差异表达的稀有转录本。这鉴定出3个RDA克隆:OsBphi237、OsBphi252和OsBphi262。DNA凝胶印迹分析表明,SNBC61中RDA克隆的位点与抗褐飞虱供体品种Samgangbyeo的等位基因相对应。表达分析表明,在褐飞虱取食期间,SNBC61中的RDA基因上调。有趣的是,利用酶切扩增多态性序列(CAPS)标记对Samgangbyeo与感褐飞虱品种Nagdongbyeo回交产生的64个SNBC近等基因系进行分析,结果表明,编码假定脂氧合酶(LOX)的OsBphi252与褐飞虱抗性共分离。我们的结果表明,OsBphi252与Bph1紧密连锁,可能有助于褐飞虱抗性的分子标记辅助选择(MAS)。

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