MS2/GmAMS1 编码一个对大豆绦虫退化很重要的 bHLH 转录因子。

IF 5.3 2区 生物学 Q1 PLANT SCIENCES Plant Cell Reports Pub Date : 2024-08-11 DOI:10.1007/s00299-024-03300-0
Junping Yu, Yan Xu, Yuanyuan Huang, Yuxue Zhu, Lulu Zhou, Yunpeng Zhang, Bingyao Li, Hao Liu, Aigen Fu, Min Xu
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摘要

关键信息:GmAMS1 是唯一的功能性 AMS,它与 GmTDF1-1 和 GmMS3 共同作用,协调大豆的直叶退化。杂交可显著提高主要农作物以及大豆 [Glycine max (L.) Merr.] 的产量。包括 ms2 在内的稳定雄性不育/雌性不育突变体是应用于大豆杂交生产的有用资源。在此,我们通过高通量测序方法确定了 MS2/GmAMS1 中两个经典突变体 ms2(埃尔多拉多)和 ms2(艾姆斯)的详细突变位点。随后,我们通过拟南芥的互补实验验证了 GmAMS1(一种 bHLH 转录因子)是大豆中唯一有功能的 AMS 成员;并阐明了其同源基因 GmAMS2 的功能障碍是由该基因编码序列中的过早终止密码子引起的。进一步的 qRT-PCR 分析和蛋白相互作用实验表明,GmAMS1 是推定的 DYT1-TDF1-AMS-MYB80/MYB103/MS188-MS1 级联模块中表达下游成员所必需的,并可能以反馈机制调控上游成员。GmAMS1可通过不同区域与GmTDF1-1和GmMS3相互作用,这有助于剖析绦虫退化过程的机制。此外,作为控制绦束发育和退化的保守级联模块的核心成员,AMS保守地存在于所有陆生植物品系中,这意味着AMS介导的信号通路在陆生植物分化之前就已经建立,这为进一步了解绦束的进化提供了线索。
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MS2/GmAMS1 encodes a bHLH transcription factor important for tapetum degeneration in soybean.

Key message: GmAMS1 is the only functional AMS and works with GmTDF1-1 and GmMS3 to orchestrate the tapetum degeneration in soybean. Heterosis could significantly increase the production of major crops as well as soybean [Glycine max (L.) Merr.]. Stable male-sterile/female-fertile mutants including ms2 are useful resources to apply in soybean hybrid production. Here, we identified the detailed mutated sites of two classic mutants ms2 (Eldorado) and ms2 (Ames) in MS2/GmAMS1 via the high-throughput sequencing method. Subsequently, we verified that GmAMS1, a bHLH transcription factor, is the only functional AMS member in soybean through the complementary experiment in Arabidopsis; and elucidated the dysfunction of its homolog GmAMS2 is caused by the premature stop codon in the gene's coding sequence. Further qRT-PCR analysis and protein-protein interaction assays indicated GmAMS1 is required for expressing downstream members in the putative DYT1-TDF1-AMS-MYB80/MYB103/MS188-MS1 cascade module, and might regulate the upstream members in a feedback mechanism. GmAMS1 could interact with GmTDF1-1 and GmMS3 via different region, which contributes to dissect the mechanism in the tapetum degeneration process. Additionally, as a core member in the conserved cascade module controlling the tapetum development and degeneration, AMS is conservatively present in all land plant lineages, implying that AMS-mediated signaling pathway has been established before land plants diverged, which provides further insight into the tapetal evolution.

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来源期刊
Plant Cell Reports
Plant Cell Reports 生物-植物科学
CiteScore
10.80
自引率
1.60%
发文量
135
审稿时长
3.2 months
期刊介绍: Plant Cell Reports publishes original, peer-reviewed articles on new advances in all aspects of plant cell science, plant genetics and molecular biology. Papers selected for publication contribute significant new advances to clearly identified technological problems and/or biological questions. The articles will prove relevant beyond the narrow topic of interest to a readership with broad scientific background. The coverage includes such topics as: - genomics and genetics - metabolism - cell biology - abiotic and biotic stress - phytopathology - gene transfer and expression - molecular pharming - systems biology - nanobiotechnology - genome editing - phenomics and synthetic biology The journal also publishes opinion papers, review and focus articles on the latest developments and new advances in research and technology in plant molecular biology and biotechnology.
期刊最新文献
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