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水稻分蘖抑制基因ts1的精细定位与候选基因分析

Fine Mapping and Candidate Gene Analysis of the Tiller Suppression Gene ts1 in Rice.

作者信息

Liu Lei, Meng Fen, He Yonggang, Zhu Menghao, Shen Yanhao, Zhang Zhihong

机构信息

State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, China.

出版信息

PLoS One. 2017 Jan 20;12(1):e0170574. doi: 10.1371/journal.pone.0170574. eCollection 2017.

Abstract

Tiller number is one of the key factors that influences rice plant type and yield components. In this study, an EMS-induced rice tiller suppression mutant ts1 was characterized. Morphological and histological observations revealed that, in the ts1 plants, the tiller buds were abnormally formed and therefore cannot outgrow into tillers. With an F2 population derived from a cross between ts1 and an indica cultivar Wushansimiao, a major gene, tiller suppression 1 (ts1) was fine-mapped to a 108.5 kb genomic region between markers ID8378 and SSR6884 on the short arm of rice chromosome 2. Candidate gene analysis identified nineteen putative genes. Among them, ORF4 (LOC_Os02g01610) is a PPR gene which harbored a point mutation c.+733/C→T in ts1 mutant plants. A co-dominant SNP marker cd-733C/T was subsequently developed and the SNP assay demonstrated that the point mutation co-segregated with tiller suppression phenotype. Quantitative RT-PCR analysis showed that the expression level of ORF4 in ts1 plants was significantly lower than that in their wild plants, and the expression of rice tillering regulators MOC1 and HTD1 was also significantly decreased in ts1 plants. Our data indicated that ORF4 was a strong candidate gene for ts1 and ts1 might play a role in regulating rice tillering through MOC1 and HTD1 associated pathway. The results above provide a basis for further functional characterization of ts1 and will shed light on molecular mechanism of rice tillering. The informative SNP marker cd-733C/T will facilitate marker-assisted selection of ts1 in rice plant type breeding.

摘要

分蘖数是影响水稻株型和产量构成因素的关键因素之一。在本研究中,对一个经甲基磺酸乙酯(EMS)诱变的水稻分蘖抑制突变体ts1进行了特征分析。形态学和组织学观察表明,在ts1植株中,分蘖芽形成异常,因此不能发育成分蘖。利用ts1与籼稻品种巫山丝苗杂交获得的F2群体,将一个主效基因——分蘖抑制1(ts1)精细定位到水稻第2染色体短臂上标记ID8378和SSR6884之间108.5 kb的基因组区域。候选基因分析鉴定出19个推定基因。其中,ORF4(LOC_Os02g01610)是一个PPR基因,在ts1突变体植株中存在一个点突变c.+733/C→T。随后开发了一个共显性SNP标记cd-733C/T,SNP分析表明该点突变与分蘖抑制表型共分离。定量RT-PCR分析表明,ts1植株中ORF4的表达水平显著低于其野生型植株,水稻分蘖调控因子MOC1和HTD1在ts1植株中的表达也显著降低。我们的数据表明,ORF4是ts1的一个强有力的候选基因,ts1可能通过与MOC1和HTD1相关的途径在调控水稻分蘖中发挥作用。上述结果为进一步对ts1进行功能鉴定提供了依据,并将有助于阐明水稻分蘖的分子机制。信息性SNP标记cd-733C/T将有助于在水稻株型育种中对ts1进行分子标记辅助选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8d1/5249193/06e46bce8ab5/pone.0170574.g001.jpg

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