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WAV E3 泛素连接酶在 TMK1 介导的生长素信号通路中介导 IAA32/34 的降解,从而调控顶端弯钩的发育。

WAV E3 ubiquitin ligases mediate degradation of IAA32/34 in the TMK1-mediated auxin signaling pathway during apical hook development.

机构信息

Ministry of Education Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University, Lanzhou 730000, People's Republic of China.

Gansu Province Key Laboratory of Gene Editing for Breeding, School of Life Sciences, Lanzhou University, Lanzhou 730000, People's Republic of China.

出版信息

Proc Natl Acad Sci U S A. 2024 Apr 23;121(17):e2314353121. doi: 10.1073/pnas.2314353121. Epub 2024 Apr 18.

DOI:10.1073/pnas.2314353121
PMID:38635634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11047095/
Abstract

Auxin regulates plant growth and development through downstream signaling pathways, including the best-known SCF-Aux/IAA-ARF pathway and several other less characterized "noncanonical" pathways. Recently, one SCF-independent noncanonical pathway, mediated by Transmembrane Kinase 1 (TMK1), was discovered through the analyses of its functions in apical hook development. Asymmetric accumulation of auxin on the concave side of the apical hook triggers DAR1-catalyzed release of the C-terminal of TMK1, which migrates into the nucleus, where it phosphorylates and stabilizes IAA32/34 to inhibit cell elongation, which is essential for full apical hook formation. However, the molecular factors mediating IAA32/34 degradation have not been identified. Here, we show that proteins in the CYTOKININ INDUCED ROOT WAVING 1 (CKRW1)/WAVY GROWTH 3 (WAV3) subfamily act as E3 ubiquitin ligases to target IAA32/34 for ubiquitination and degradation, which is inhibited by TMK1c-mediated phosphorylation. This antagonistic interaction between TMK1c and CKRW1/WAV3 subfamily E3 ubiquitin ligases regulates IAA32/34 levels to control differential cell elongation along opposite sides of the apical hook.

摘要

生长素通过下游信号通路调节植物的生长和发育,包括最著名的 SCF-Aux/IAA-ARF 通路和几个其他特征不太明显的“非经典”通路。最近,通过分析其在顶端弯钩发育中的功能,发现了一条不依赖于 SCF 的非经典通路,该通路由跨膜激酶 1 (TMK1) 介导。生长素在顶端弯钩凹面的不对称积累触发 DAR1 催化的 TMK1 羧基端释放,TMK1 迁移到细胞核内,在细胞核内它磷酸化并稳定 IAA32/34 以抑制细胞伸长,这对于完全形成顶端弯钩至关重要。然而,介导 IAA32/34 降解的分子因素尚未确定。在这里,我们表明细胞分裂素诱导根波动 1 (CKRW1)/波浪生长 3 (WAV3) 亚家族中的蛋白作为 E3 泛素连接酶,将 IAA32/34 靶向泛素化和降解,这一过程受 TMK1c 介导的磷酸化抑制。TMK1c 和 CKRW1/WAV3 亚家族 E3 泛素连接酶之间的这种拮抗相互作用调节 IAA32/34 水平,以控制顶端弯钩相对两侧的细胞伸长的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/f5c4b8acf22e/pnas.2314353121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/a289d3335407/pnas.2314353121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/bb9c08f9b5f7/pnas.2314353121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/c53ebdb27621/pnas.2314353121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/c2f980171eff/pnas.2314353121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/2bb510484288/pnas.2314353121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/f5c4b8acf22e/pnas.2314353121fig06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/a289d3335407/pnas.2314353121fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/bb9c08f9b5f7/pnas.2314353121fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/c53ebdb27621/pnas.2314353121fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/c2f980171eff/pnas.2314353121fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/2bb510484288/pnas.2314353121fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5c8/11047095/f5c4b8acf22e/pnas.2314353121fig06.jpg

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