Key Laboratory of Soybean Molecular Design Breeding, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, Harbin, 150081, China.
Horticulture Department, College of Advanced Agriculture and Ecological Environment, Heilongjiang University, 74 Xuefu Road, Harbin, 150000, Heilongjiang, China.
Theor Appl Genet. 2023 Mar 13;136(3):56. doi: 10.1007/s00122-023-04255-8.
A novel splice-site mutation in the P. vulgarisgene for TETRAKETIDE α-PYRONE REDUCTASE 2 impairs male fertility, and parthenocarpic pod development can be improved by external application of IAA. Snap bean (Phaseolus vulgaris L.) is an important vegetable crop in many parts of the world, and the main edible part is the fresh pod. Here, we report the characterization of the genic male sterility (ms-2) mutant in common bean. Loss of function of MS-2 accelerates degradation of the tapetum, resulting in a complete male sterility. Through fine-mapping, co-segregation, and re-sequencing analysis, we identified Phvul.003G032100, which encodes the TETRAKETIDE α-PYRONE REDUCTASE 2 (PvTKPR2) protein in common bean, as the causal gene for MS-2. PvTKPR2 is predominantly expressed at the early stages of flower development. A novel 7-bp (+ 6028 bp to + 6034 bp) deletion mutation spans the splice site between the fourth intron and fifth exon, leading to a 9-bp deletion in transcribed mRNA and a 3-amino acid (G210M211V212) deletion in the protein coding sequence of the PvTKPR2 gene. The 3-D structural changes in the protein due to the mutation may impair the activities of NAD-dependent epimerase/dehydratase and the NAD(P)-binding domains of PvTKPR2 protein. The ms-2 mutant plants produce many small parthenocarpic pods, and the size of the pods can be doubled by external application of 2 mM indole-3-acetic acid (IAA). Our results demonstrate that a novel mutation in PvTKPR2 impairs male fertility through premature degradation of the tapetum.
豌豆 Tetraketide α-吡喃酮还原酶 2 基因的新型剪接位点突变导致雄性不育,而外源施加 IAA 可改善单性结实豆荚的发育。菜豆(Phaseolus vulgaris L.)是世界许多地区的重要蔬菜作物,主要可食用部分是新鲜豆荚。本研究报道了普通菜豆基因雄性不育(ms-2)突变体的特征。MS-2 基因的功能丧失加速了绒毡层的降解,导致完全雄性不育。通过精细定位、共分离和重测序分析,我们鉴定出 Phvul.003G032100 编码普通菜豆的 Tetraketide α-吡喃酮还原酶 2(PvTKPR2)蛋白,是 MS-2 的候选基因。PvTKPR2 在花发育的早期阶段主要表达。一个新的 7-bp(+6028 bp 到+6034 bp)缺失突变跨越第四内含子和第五外显子的剪接位点,导致转录 mRNA 中 9-bp 的缺失和 PvTKPR2 基因编码序列中 3 个氨基酸(G210M211V212)的缺失。由于突变导致的蛋白 3-D 结构变化可能会损害 PvTKPR2 蛋白的 NAD 依赖性差向异构酶/脱水酶和 NAD(P)-结合结构域的活性。ms-2 突变体植株产生许多小的单性结实豆荚,通过外源施加 2 mM 吲哚-3-乙酸(IAA)可使豆荚的大小加倍。研究结果表明,PvTKPR2 中的新型突变通过绒毡层的过早降解导致雄性不育。