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野生稻 中一个自发突变的雄性不育基因的遗传分析和精细定位

Genetic Analysis and Fine Mapping of a Spontaneously Mutated Male Sterility Gene in ssp. .

机构信息

Department of Agronomy, National Taiwan University, Taipei, Taiwan, R.O.C. 10617.

Institute of Ecology and Evolutionary Biology, National Taiwan University, Taipei, Taiwan, R.O.C.

出版信息

G3 (Bethesda). 2020 Apr 9;10(4):1309-1318. doi: 10.1534/g3.120.401091.

Abstract

Male sterility has been widely used in hybrid seed production in Brassica, but not in ssp. , and genetic models of male sterility for this subspecies are unclear. We discovered a spontaneous mutant in ssp. A series of progeny tests indicated that male sterility in ssp. follows a three-allele model with , , and The male sterility locus has been mapped to chromosome A07 in BC and F populations through genotyping by sequencing. Fine mapping in a total of 1,590 F plants narrowed the male sterility gene to a 400 kb region, with two SNP markers only 0.3 cM from the gene. Comparative gene mapping shows that the gene in ssp. is different from the gene of ssp. , despite that both genes are located on chromosome A07. Interestingly, the DNA sequence orthologous to a male sterile gene in , , is within 400 kb of the locus. The orthologs of ssp. were sequenced, and one KASP marker (BrMs_indel) was developed for genotyping based on a 14 bp indel at intron 4. Cosegregation of male sterility and BrMs_indel genotypes in the F population indicated that from and from are likely to be orthologs. The BrMs_indel marker developed in this study will be useful in marker-assisted selection for the male sterility trait.

摘要

雄性不育在芸薹属杂种种子生产中得到了广泛应用,但在 亚种中没有应用,而且该亚种雄性不育的遗传模型还不清楚。我们在 亚种中发现了一个自发突变体。一系列后代测试表明, 亚种的雄性不育遵循三等位基因模型,具有 、 和 。雄性不育基因座已通过测序基因分型被映射到 BC 和 F 群体的 A07 染色体上。在总共 1590 株 F 代植物中的精细定位将雄性不育基因缩小到 400kb 区域,两个 SNP 标记距离基因仅 0.3cM。比较基因作图表明, 亚种中的 基因与 亚种中的 基因不同,尽管这两个基因都位于 A07 染色体上。有趣的是,在 中与雄性不育基因同源的 DNA 序列在 400kb 内与 基因座。对 亚种的 基因进行了测序,并根据第 4 内含子中的 14bp 缺失开发了一个 KASP 标记(BrMs_indel)用于基因分型。F 群体中雄性不育和 BrMs_indel 基因型的共分离表明, 和 来自 和 可能是同源基因。本研究中开发的 BrMs_indel 标记将有助于雄性不育性状的标记辅助选择。

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