Identification of a gene coding for a pentatricopeptide repeat protein as a candidate responsible for the Ms2, a novel restorer-of-fertility locus in onion (Allium cepa L.).

IF 2.6 3区 农林科学 Q1 AGRONOMY
Molecular Breeding Pub Date : 2025-04-05 eCollection Date: 2025-04-01 DOI:10.1007/s11032-025-01561-5
Geonjoong Kim, Sunggil Kim
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引用次数: 0

Abstract

Ms and Ms2 are restorer-of-fertility loci in onion (Allium cepa L.); additionally, Ms2 is responsible for unstable male fertility in some accessions. Although a candidate gene was previously reported for the Ms locus, the gene responsible for the Ms2 locus remains unidentified. A 12.5 Mb genomic region harboring the Ms2 locus was initially obtained from onion whole genome sequences using two flanking markers to identify candidates. This region was further delimited to 3.19 Mb via fine mapping using 12 recombinants and 11 additional markers. A gene coding for a pentatricopeptide repeat (PPR) protein was identified within the 3.19 Mb region and designated AcPPR876. Phylogenetic analysis showed that AcPPR876 and four homologs belonged to the Rf-like PPR gene family. Polymorphic sequences between male fertile (MF) and male sterile (MS) AcPPR876 alleles were concentrated in the 5' region of the gene. Among them, a 446 bp insertion was identified at the putative promoter region of the MF allele. Although overall AcPPR876 transcription levels were very low, transcription levels of the MF allele were generally higher than those of the MS allele. A simple PCR marker was developed using the 446 bp insertion to perform Ms2 locus genotyping in the diverse onion germplasm. Although the dominant Ms2 allele was not found in any of the 250 domestic breeding lines, 29 out of 108 exotic accessions were shown to contain the dominant Ms2 alleles. Overall, the AcPPR876 gene is proposed as a strong candidate for the Ms2 locus.

Supplementary information: The online version contains supplementary material available at 10.1007/s11032-025-01561-5.

洋葱(Allium cepa L.)新育性恢复位点Ms2编码五肽重复蛋白候选基因的鉴定。
Ms和Ms2是洋葱(Allium cepa L.)的育性恢复位点;此外,在一些品种中,Ms2是导致雄性生育力不稳定的原因。虽然先前报道了Ms位点的候选基因,但负责Ms2位点的基因仍未确定。利用两个侧翼标记从洋葱全基因组序列中获得了包含Ms2位点的12.5 Mb基因组区域。通过12个重组体和11个附加标记的精细定位,进一步将该区域划分为3.19 Mb。在3.19 Mb的区域内鉴定出一个编码五肽重复(PPR)蛋白的基因,命名为AcPPR876。系统发育分析表明,AcPPR876和4个同源基因属于rf样PPR基因家族。AcPPR876雄性可育(MF)和雄性不育(MS)等位基因之间的多态性序列集中在该基因的5′区。其中,在MF等位基因的推定启动子区域发现了一个446 bp的插入。虽然AcPPR876的总体转录水平很低,但MF等位基因的转录水平普遍高于MS等位基因。利用446 bp的插入,建立了一个简单的PCR标记,对不同洋葱种质进行Ms2位点基因分型。虽然在250个国内选育系中均未发现显性Ms2等位基因,但在108个外来选育系中有29个含有显性Ms2等位基因。总的来说,AcPPR876基因被认为是Ms2位点的一个强有力的候选者。补充资料:在线版本包含补充资料,下载地址:10.1007/s11032-025-01561-5。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Breeding
Molecular Breeding 农林科学-农艺学
CiteScore
5.60
自引率
6.50%
发文量
67
审稿时长
1.5 months
期刊介绍: Molecular Breeding is an international journal publishing papers on applications of plant molecular biology, i.e., research most likely leading to practical applications. The practical applications might relate to the Developing as well as the industrialised World and have demonstrable benefits for the seed industry, farmers, processing industry, the environment and the consumer. All papers published should contribute to the understanding and progress of modern plant breeding, encompassing the scientific disciplines of molecular biology, biochemistry, genetics, physiology, pathology, plant breeding, and ecology among others. Molecular Breeding welcomes the following categories of papers: full papers, short communications, papers describing novel methods and review papers. All submission will be subject to peer review ensuring the highest possible scientific quality standards. Molecular Breeding core areas: Molecular Breeding will consider manuscripts describing contemporary methods of molecular genetics and genomic analysis, structural and functional genomics in crops, proteomics and metabolic profiling, abiotic stress and field evaluation of transgenic crops containing particular traits. Manuscripts on marker assisted breeding are also of major interest, in particular novel approaches and new results of marker assisted breeding, QTL cloning, integration of conventional and marker assisted breeding, and QTL studies in crop plants.
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