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一个 PHD-finger 蛋白 MS4 的突变导致大豆雄性不育。

Mutation in a PHD-finger protein MS4 causes male sterility in soybean.

机构信息

Fiber and Biopolymer Research Institute, Department of Plant and Soil Science, Texas Tech University, Lubbock, TX, 79409, USA.

US Salinity Laboratory (USDA-ARS), Riverside, CA, 92507, USA.

出版信息

BMC Plant Biol. 2019 Aug 28;19(1):378. doi: 10.1186/s12870-019-1979-4.

Abstract

BACKGROUND

Male sterility has tremendous scientific and economic importance in hybrid seed production. Identification and characterization of a stable male sterility gene will be highly beneficial for making hybrid seed production economically feasible. In soybean, eleven male-sterile, female-fertile mutant lines (ms1, ms2, ms3, ms4, ms5, ms6, ms7, ms8, ms9, msMOS, and msp) have been identified and mapped onto various soybean chromosomes, however the causal genes responsible for male sterility are not isolated. The objective of this study was to identify and functionally characterize the gene responsible for the male sterility in the ms4 mutant.

RESULTS

The ms4 locus was fine mapped to a 216 kb region, which contains 23 protein-coding genes including Glyma.02G243200, an ortholog of Arabidopsis MALE MEIOCYTE DEATH 1 (MMD1), which is a Plant Homeodomain (PHD) protein involved in male fertility. Isolation and sequencing of Glyma.02G243200 from the ms4 mutant line showed a single base insertion in the 3rd exon causing a premature stop codon resulting in truncated protein production. Phylogenetic analysis showed presence of a homolog protein (MS4_homolog) encoded by the Glyma.14G212300 gene. Both proteins were clustered within legume-specific clade of the phylogenetic tree and were likely the result of segmental duplication during the paleoploidization events in soybean. The comparative expression analysis of Ms4 and Ms4_homologs across the soybean developmental and reproductive stages showed significantly higher expression of Ms4 in early flowering (flower bud differentiation) stage than its homolog. The functional complementation of Arabidopsis mmd1 mutant with the soybean Ms4 gene produced normal stamens, successful tetrad formation, fertile pollens and viable seeds, whereas the Ms4_homolog was not able to restore male fertility.

CONCLUSIONS

Overall, this is the first report, where map based cloning approach was employed to isolate and characterize a gene responsible for the male-sterile phenotype in soybean. Characterization of male sterility genes may facilitate the establishment of a stable male sterility system, highly desired for the viability of hybrid seed production in soybean. Additionally, translational genomics and genome editing technologies can be utilized to generate new male-sterile lines in other plant species.

摘要

背景

雄性不育在杂交种子生产中具有巨大的科学和经济意义。鉴定和描述稳定的雄性不育基因将非常有利于使杂交种子生产在经济上可行。在大豆中,已经鉴定和定位了 11 个雄性不育、雌性可育的突变系(ms1、ms2、ms3、ms4、ms5、ms6、ms7、ms8、ms9、msMOS 和 msp)到不同的大豆染色体上,但导致雄性不育的原因基因尚未分离。本研究的目的是鉴定和功能表征 ms4 突变体雄性不育的相关基因。

结果

ms4 基因座被精细定位到一个 216kb 的区域,该区域包含 23 个编码蛋白的基因,包括 Glyma.02G243200,它是拟南芥雄性减数分裂 1(MMD1)的同源物,是一种参与雄性育性的植物同源结构域(PHD)蛋白。从 ms4 突变体系中分离和测序 Glyma.02G243200 显示第 3 外显子的单个碱基插入导致提前终止密码子,从而产生截短的蛋白质产物。系统发育分析显示 Glyma.14G212300 基因编码的同源蛋白(MS4_homolog)的存在。这两种蛋白质都聚集在系统发育树的豆科特异性分支中,可能是大豆古多倍体化过程中片段复制的结果。在大豆发育和生殖阶段,Ms4 和 Ms4_homologs 的比较表达分析表明,Ms4 在早期开花(花芽分化)阶段的表达显著高于其同源物。用大豆 Ms4 基因对拟南芥 mmd1 突变体的功能互补产生了正常的雄蕊、成功的四分体形成、可育花粉和有活力的种子,而 Ms4_homolog 则不能恢复雄性育性。

结论

总体而言,这是首次采用基于图谱的克隆方法分离和鉴定大豆雄性不育表型的相关基因。雄性不育基因的鉴定可能有助于建立稳定的雄性不育系统,这对大豆杂交种子生产的可行性非常重要。此外,还可以利用转化基因组学和基因组编辑技术在其他植物物种中产生新的雄性不育系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1929/6712664/18be7e250e3a/12870_2019_1979_Fig1_HTML.jpg

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