The E3 ligase TaE3V-B1 ubiquitinates proteins encoded by the vernalization gene TaVRN1 and regulates developmental processes in wheat.

IF 6.5 1区 生物学 Q1 PLANT SCIENCES
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

Abstract

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 3 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.

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。
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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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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