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Melatonin‐mediated CcARP1 alters F‐actin dynamics by phosphorylation of CcADF9 to balance root growth and salt tolerance in pigeon pea.

Authors :
Cao, Hongyan
Yang, Qing
Wang, Tianyi
Du, Tingting
Song, Zhihua
Dong, Biying
Chen, Ting
Wei, Yifan
Xue, Jingyi
Meng, Dong
Fu, Yujie
Source :
Plant Biotechnology Journal; Jan2024, Vol. 22 Issue 1, p98-115, 18p
Publication Year :
2024

Abstract

Summary: As a multifunctional hormone‐like molecule, melatonin exhibits a pleiotropic role in plant salt stress tolerance. While actin cytoskeleton is essential to plant tolerance to salt stress, it is unclear if and how actin cytoskeleton participates in the melatonin‐mediated alleviation of plant salt stress. Here, we report that melatonin alleviates salt stress damage in pigeon pea by activating a kinase‐like protein, which interacts with an actin‐depolymerizing factor. Cajanus cajan Actin‐Depolymerizing Factor 9 (CcADF9) has the function of severing actin filaments and is highly expressed under salt stress. The CcADF9 overexpression lines (CcADF9‐OE) showed a reduction of transgenic root length and an increased sensitivity to salt stress. By using CcADF9 as a bait to screen an Y2H library, we identified actin depolymerizing factor‐related phosphokinase 1 (ARP1), a novel protein kinase that interacts with CcADF9. CcARP1, induced by melatonin, promotes salt resistance of pigeon pea through phosphorylating CcADF9, inhibiting its severing activity. The CcARP1 overexpression lines (CcARP1‐OE) displayed an increased transgenic root length and resistance to salt stress, whereas CcARP1 RNA interference lines (CcARP1‐RNAi) presented the opposite phenotype. Altogether, our findings reveal that melatonin‐induced CcARP1 maintains F‐actin dynamics balance by phosphorylating CcADF9, thereby promoting root growth and enhancing salt tolerance. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14677644
Volume :
22
Issue :
1
Database :
Complementary Index
Journal :
Plant Biotechnology Journal
Publication Type :
Academic Journal
Accession number :
174515148
Full Text :
https://doi.org/10.1111/pbi.14170