染色体易位是水稻杂交不育的重要驱动因素。

IF 5.1 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-09-03 DOI:10.1093/genetics/iyaf126
Zhenwei Xie, Hai Zheng, Siqi Cheng, Hao Yu, Xiaowen Yu, Chaolong Wang, Jian Wang, Bowen Yao, Xiaokang Jiang, Yang Hu, Anqi Jian, Xiaodong He, Junwen Gao, Minrui Chen, Yun Chen, Yuantao Zhu, Yulong Ren, Zhijun Cheng, Cailin Lei, Qibing Lin, Xin Wang, Xiuping Guo, Yunlu Tian, Shijia Liu, Xi Liu, Ling Jiang, Chuanyin Wu, Shanshan Zhu, Zhigang Zhao, Jianmin Wan
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引用次数: 0

摘要

杂种不育是利用远亲杂交产生的水稻杂种优势的主要障碍。虽然诸如杀手-保护系统之类的遗传机制已经得到了广泛的研究,但杂种不育的新系统仍然缺乏特征。本文报道了一种新的杂交不育系统,该系统由两个紧密假连锁位点SGA1(位于1号染色体上)和SGA2(位于2号染色体上)控制,在籼稻和粳稻亚种杂交过程中诱导雄性和雌性配子半不育。染色体易位被认为是假连锁和无偏分离的基础,并得到减数分裂四价结构和易位断点序列的细胞学证据的支持。配子体不育被认为是易位杂合子双雄半不育的主要驱动因素。此外,发现大片段染色体易位在水稻中广泛存在。对120份全基因组水稻材料的分析表明,染色体易位在水稻品种中普遍存在,其中三分之一的水稻品种出现大易位(> - 500 kb)。易位断点主要位于基因间区和内含子区,被破坏的基因主要为转座子和反转录转座子。此外,通过序列分析和表型分析验证了大易位。总的来说,本研究确立了染色体易位是杂种不育的关键驱动因素,并为杂种优势制约提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chromosomal translocations are a significant driver of hybrid sterility in rice.

Hybrid sterility is a major barrier in exploiting hybrid vigor in rice grains produced by crossing distantly related parents. While genetic mechanisms such as the killer-protector system have been extensively studied, novel systems underlying hybrid sterility remain poorly characterized. Here, a novel hybrid sterility system governed by two tightly pseudolinked loci SGA1 (on chromosome 1) and SGA2 (on chromosome 2) is reported, which induces semi-sterility in male and female gametes during hybridization between the indica and japonica subspecies. Chromosomal translocations were proposed as the basis for pseudolinkage and unbiased segregation, supported by cytological evidence of meiotic quadrivalent configurations and translocation breakpoint sequences. Gametophytic sterility was identified as the primary driver of dual male-female semi-sterility in translocated heterozygotes. Furthermore, large-segment chromosomal translocations are found to be widespread in rice. Analysis of 120 pangenomic rice accessions revealed that chromosomal translocations are prevalent among cultivars, with one-third exhibiting large translocations (>500 kb). Translocation breakpoints were mainly localized in intergenic and intronic regions, and the disrupted genes were identified as predominantly transposons and retrotransposons. Besides, large translocations were validated through sequence analysis and phenotypic assays. Overall, this study establishes chromosomal translocations as a critical driver of hybrid sterility and provides new insights into heterosis constraints.

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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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