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一个控制水稻穗顶端败育的新的主要数量性状位点的精细定位

Fine Mapping of a Novel Major Quantitative Trait Locus, , That Controls Panicle Apical Abortion in Rice.

作者信息

Wang Xiaolei, Li Lingfeng, Sun Xiaotang, Xu Jie, Ouyang Linjuan, Bian Jianmin, Chen Xiaorong, Li Weixing, Peng Xiaosong, Hu Lifang, Cai Yicong, Zhou Dahu, He Xiaopeng, Fu Junru, Fu Haihui, He Haohua, Zhu Changlan

机构信息

Key Laboratory of Crop Physiology, Ecology and Genetic Breeding, Ministry of Education, College of Agronomy, Jiangxi Agricultural University, Nanchang, China.

出版信息

Front Plant Sci. 2021 Jul 7;12:683329. doi: 10.3389/fpls.2021.683329. eCollection 2021.

Abstract

The panicle apical abortion (PAA) causes severe yield losses in rice production, but details about its development and molecular basis remain elusive. Here, we detected PAA quantitative trait loci (QTLs) in three environments using a set of chromosome segment substitution lines (CSSLs) that was constructed with Changhui121 as the recurrent parent and Koshihikari as the donor parent. First, we identified a novel major effector quantitative trait locus, , and selected a severe PAA line, CSSL176, which had the highest PAA rate among CSSLs having Koshihikari segments at this locus. Next, an F population was constructed from a cross between CSS176 and CH121. Using F to make recombinantion analysis, was mapped to an 73.8-kb interval in chromosome 7. Among nine candidate genes within this interval, there isn't any known genes affecting PAA. According to the gene annotation, gene expression profile and alignment of genomic DNA, and were predicted as putative candidate genes of . Our study provides a foundation for cloning and functional characterization of the target gene from this locus.

摘要

穗顶部败育(PAA)在水稻生产中导致严重的产量损失,但其发育和分子基础的细节仍然难以捉摸。在这里,我们使用一组染色体片段代换系(CSSLs)在三种环境中检测了PAA数量性状位点(QTLs),该代换系是以长恢121为轮回亲本、越光为供体亲本构建的。首先,我们鉴定出一个新的主要效应数量性状位点,并选择了一个严重PAA系CSSL176,它在该位点具有越光片段的CSSLs中PAA率最高。接下来,从CSS176和CH121的杂交中构建了一个F群体。利用F进行重组分析,将其定位到第7号染色体上一个73.8 kb的区间内。在该区间内的9个候选基因中,没有任何已知影响PAA的基因。根据基因注释、基因表达谱和基因组DNA比对,预测LOC_Os07g43180和LOC_Os07g43190为该位点的假定候选基因。我们的研究为从该位点克隆目标基因并进行功能表征奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bf1/8293750/55e9e7da48b5/fpls-12-683329-g001.jpg

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