E3连接酶TaE3V-B1泛素化春化基因TaVRN1编码的蛋白,并调控小麦的发育过程。

IF 6.5 1区 生物学 Q1 PLANT SCIENCES Plant Physiology Pub Date : 2024-11-18 DOI:10.1093/plphys/kiae606
Tian Li, Ragupathi Nagarajan, Shujuan Liu, Juan C Luzuriaga, Wenxuan Zhai, Shuanghe Cao, Haiyan Jia, Brett F Carver, Liuling Yan
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引用次数: 0

摘要

在小麦(Triticum aestivum)中,人们希望小麦早熟,以避开炎热干燥的夏季,特别是考虑到气候变化。在这里,我们报告了与 TaVRN1 相互作用的 C3H2C3 RING 型 E3 连接酶 TaE3V1 与小麦的早期发育有关。除了其 RING 结构域外,TaE3V1 并不包含其他 RING 型或其他 E3 连接酶蛋白中的保守结构域。由功能性 TaE3V1 等位基因编码的 TaE3V-B1b 与 TaVRN1 相互作用并泛素化 TaVRN1。相反,由天然无功能 TaE3V1 等位基因编码的 TaE3V-B1a 既不与 TaVRN1 相互作用,也没有 E3 连接酶活性。在温度较高的情况下,TaE3V-B1b 的活性会随着植株年龄的增长而降低,但在春化所需的低温条件下则不会。我们采用基因编辑方法同时使三个同源的 TaE3V1 基因失活,以验证它们的功能。总之,我们的研究结果表明,自然突变和编辑的 TaE3V1 等位基因可以加速小麦的生长发育,帮助小麦适应气候变暖。
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The E3 ligase TaE3V-B1 ubiquitinates proteins encoded by the vernalization gene TaVRN1 and regulates developmental processes in wheat.

In wheat (Triticum aestivum), early maturity is desired to avoid the hot and dry summer season, especially in view of climate change. Here, we report that TaE3V1, a C3H2C3 RING-type E3 ligase that interacts with TaVRN1, is associated with early development. Aside from its RING domain, TaE3V1 does not harbor any domains that are conserved in other RING-type or other E3 ligase proteins. TaE3V-B1b, encoded by the functional TaE3V1 allele, interacts with and ubiquitinates TaVRN1. In contrast, TaE3V-B1a, encoded by a natural nonfunctional TaE3V1 allele, neither interacts with TaVRN1 nor has E3 ligase activity. TaE3V-B1b activity decreases with plant age under warmer temperatures, but not under the low temperatures required for vernalization. We employed a gene editing method to simultaneously inactivate the three homoeologous TaE3V1 genes to validate their functions. Overall, our results suggest that the naturally mutated and edited TaE3V1 alleles can accelerate wheat development and aid adaptation to warming climates.

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来源期刊
Plant Physiology
Plant Physiology 生物-植物科学
CiteScore
12.20
自引率
5.40%
发文量
535
审稿时长
2.3 months
期刊介绍: Plant Physiology® is a distinguished and highly respected journal with a rich history dating back to its establishment in 1926. It stands as a leading international publication in the field of plant biology, covering a comprehensive range of topics from the molecular and structural aspects of plant life to systems biology and ecophysiology. Recognized as the most highly cited journal in plant sciences, Plant Physiology® is a testament to its commitment to excellence and the dissemination of groundbreaking research. As the official publication of the American Society of Plant Biologists, Plant Physiology® upholds rigorous peer-review standards, ensuring that the scientific community receives the highest quality research. The journal releases 12 issues annually, providing a steady stream of new findings and insights to its readership.
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