QTL Detection for Rice Grain Length and Fine Mapping of a Novel Locus qGL6.1.

Mingzhu Zhao, Yuanzheng Wang, Na He, Xiu Pang, Lili Wang, Zuobin Ma, Zhiqiang Tang, Hong Gao, Liying Zhang, Liang Fu, Changhua Wang, Jingang Liu, Wenjing Zheng
{"title":"QTL Detection for Rice Grain Length and Fine Mapping of a Novel Locus qGL6.1.","authors":"Mingzhu Zhao,&nbsp;Yuanzheng Wang,&nbsp;Na He,&nbsp;Xiu Pang,&nbsp;Lili Wang,&nbsp;Zuobin Ma,&nbsp;Zhiqiang Tang,&nbsp;Hong Gao,&nbsp;Liying Zhang,&nbsp;Liang Fu,&nbsp;Changhua Wang,&nbsp;Jingang Liu,&nbsp;Wenjing Zheng","doi":"10.1186/s12284-022-00606-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Grain length (GL) that is directly associated with appearance quality is a key target of selection in rice breeding. Although abundant quantitative trait locus (QTL) associated with GL have been identified, it was still relatively weak to identify QTL for GL from japonica genetic background, as the shortage of japonica germplasms with long grains. We performed QTLs analysis for GL using a recombinant inbred lines (RILs) population derived from the cross between japonica variety GY8 (short grains) and LX1 (long grains) in four environments.</p><p><strong>Results: </strong>A total of 197 RILs were genotyped with 285 polymorphic SNP markers. Three QTLs qGL5.3, qGL6.1 and qGL11 were detected to control GL by individual environmental analyses and multi-environment joint analysis. Of these, a major-effect and stable QTL qGL6.1 was identified to be a novel QTL, and its LX1 allele had a positive effect on GL. For fine-mapping qGL6.1, a BC<sub>1</sub>F<sub>2</sub> population consisting of 2,487 individuals was developed from a backcross between GY8 and R176, one line with long grain. Eight key informative recombinants were identified by nine kompetitive allele specific PCR (KASP) markers. By analyzing key recombinants, the qGL6.1 locus was narrowed down to a 40.41 kb genomic interval on chromosome 6. One candidate gene LOC_Os06g43304.1 encoding cytochrome P450 (CYP71D55) was finally selected based on the difference in the transcriptional expression and variations in its upstream and downstream region.</p><p><strong>Conclusions: </strong>Three QTLs qGL5.3, qGL6.1 and qGL11 were identified to control grain length in rice. One novel QTL qGL6.1 was fine mapped within 40.41 kb region, and LOC_Os06g43304.1 encoding cytochrome P450 (CYP71D55) may be its candidate gene. We propose that the further cloning of the qGL6.1 will facilitate improving appearance quality in japonica varieties.</p>","PeriodicalId":520771,"journal":{"name":"Rice (New York, N.Y.)","volume":" ","pages":"60"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705657/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rice (New York, N.Y.)","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1186/s12284-022-00606-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Grain length (GL) that is directly associated with appearance quality is a key target of selection in rice breeding. Although abundant quantitative trait locus (QTL) associated with GL have been identified, it was still relatively weak to identify QTL for GL from japonica genetic background, as the shortage of japonica germplasms with long grains. We performed QTLs analysis for GL using a recombinant inbred lines (RILs) population derived from the cross between japonica variety GY8 (short grains) and LX1 (long grains) in four environments.

Results: A total of 197 RILs were genotyped with 285 polymorphic SNP markers. Three QTLs qGL5.3, qGL6.1 and qGL11 were detected to control GL by individual environmental analyses and multi-environment joint analysis. Of these, a major-effect and stable QTL qGL6.1 was identified to be a novel QTL, and its LX1 allele had a positive effect on GL. For fine-mapping qGL6.1, a BC1F2 population consisting of 2,487 individuals was developed from a backcross between GY8 and R176, one line with long grain. Eight key informative recombinants were identified by nine kompetitive allele specific PCR (KASP) markers. By analyzing key recombinants, the qGL6.1 locus was narrowed down to a 40.41 kb genomic interval on chromosome 6. One candidate gene LOC_Os06g43304.1 encoding cytochrome P450 (CYP71D55) was finally selected based on the difference in the transcriptional expression and variations in its upstream and downstream region.

Conclusions: Three QTLs qGL5.3, qGL6.1 and qGL11 were identified to control grain length in rice. One novel QTL qGL6.1 was fine mapped within 40.41 kb region, and LOC_Os06g43304.1 encoding cytochrome P450 (CYP71D55) may be its candidate gene. We propose that the further cloning of the qGL6.1 will facilitate improving appearance quality in japonica varieties.

Abstract Image

Abstract Image

Abstract Image

水稻粒长QTL检测及新位点qGL6.1的精细定位。
背景:籽粒长度(GL)是水稻育种中与外观品质直接相关的一个重要选择指标。虽然目前已经发现了大量与谷粒病相关的QTL,但由于长粒粳稻种质资源的缺乏,从粳稻遗传背景中鉴定谷粒病的QTL仍然相对薄弱。利用粳稻品种GY8(短粒)与LX1(长粒)杂交的重组自交系(RILs)群体,在4种环境下对GL进行了qtl分析。结果:共对197个ril进行了285个多态性SNP标记的基因分型。通过单环境分析和多环境联合分析,检测到控制GL的qGL5.3、qGL6.1和qGL11 3个qtl。其中,具有显著效应的稳定QTL qGL6.1是一个新QTL,其LX1等位基因对GL有正向影响。为精细定位qGL6.1,利用GY8与R176的一个长粒系回交构建了一个包含2487个个体的BC1F2群体。9个竞争性等位基因特异性PCR (KASP)标记鉴定出8个关键信息重组。通过分析关键重组位点,qGL6.1定位于6号染色体上40.41 kb的基因组区间。根据其上下游区域的转录表达差异和变异,最终选择了一个编码细胞色素P450 (CYP71D55)的候选基因LOC_Os06g43304.1。结论:鉴定出qGL5.3、qGL6.1和qGL11 3个控制水稻粒长的qtl。一个新的QTL qGL6.1在40.41 kb的区域被精细定位,编码细胞色素P450 (CYP71D55)的LOC_Os06g43304.1可能是其候选基因。我们认为qGL6.1的进一步克隆将有助于提高粳稻品种的外观品质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信