Suppr超能文献

R2R3-MYB 转录因子 GmMYB68 参与大豆异黄酮的积累。

R2R3-MYB transcription factor GmMYB68 is involved in the accumulation of soybean isoflavones.

机构信息

College of Plant Science, Jilin University, Changchun, China.

Changchun Culture Square Greening Management Center, Changchun, China.

出版信息

Plant Physiol Biochem. 2024 Nov;216:109187. doi: 10.1016/j.plaphy.2024.109187. Epub 2024 Oct 12.

Abstract

We aimed to investigate the regulatory function of the soybean transcription factor R2R3-MYB (GmMYB68) in isoflavone biosynthesis. Through comprehensive subcellular and chromosomal localization analyses, we found that GmMYB68 was predominantly localized to the nucleus and mapped to chromosome Gm04. Notably, SSR markers near this gene significantly correlated with seed isoflavone content. GmMYB68 overexpression markedly increased isoflavone contents, confirming its positive role in regulating isoflavone synthesis. GmMYB68 also played a crucial role in the response of soybean to abiotic stress. Using RNA-seq and yeast one-hybrid techniques, we discovered an intricate interaction between GmMYB68 and key isoflavone biosynthesis genes GmCHS7 and GmCHS8. These findings provide novel insights into the mechanisms underlying isoflavone biosynthesis. Furthermore, using yeast two-hybrid experiments, we identified proteins interacting with GmMYB68, suggesting roles in the synthesis of physiologically active compounds and abiotic stress response. We not only elucidated the regulatory mechanisms of GmMYB68 in isoflavone biosynthesis and abiotic stress response but also constructed a molecular network encompassing GmMYB68, GmCHS7, and GmCHS8. This network provides a theoretical basis for a better understanding of and strategies for improving soybean isoflavone biosynthesis.

摘要

我们旨在研究大豆转录因子 R2R3-MYB(GmMYB68)在异黄酮生物合成中的调控功能。通过全面的亚细胞和染色体定位分析,我们发现 GmMYB68 主要定位于细胞核,并定位于染色体 Gm04 上。值得注意的是,该基因附近的 SSR 标记与种子异黄酮含量显著相关。GmMYB68 的过表达显著增加了异黄酮含量,证实了其在调节异黄酮合成中的积极作用。GmMYB68 在大豆对非生物胁迫的响应中也起着至关重要的作用。通过 RNA-seq 和酵母单杂交技术,我们发现 GmMYB68 与异黄酮生物合成关键基因 GmCHS7 和 GmCHS8 之间存在复杂的相互作用。这些发现为异黄酮生物合成的机制提供了新的见解。此外,通过酵母双杂交实验,我们鉴定出与 GmMYB68 相互作用的蛋白质,表明其在生理活性化合物合成和非生物胁迫响应中的作用。我们不仅阐明了 GmMYB68 在异黄酮生物合成和非生物胁迫响应中的调控机制,还构建了一个包含 GmMYB68、GmCHS7 和 GmCHS8 的分子网络。该网络为更好地理解和改善大豆异黄酮生物合成提供了理论基础。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验