Intrinsically disordered proteins SAID1/2 condensate on SERRATE for dual inhibition of miRNA biogenesis in Arabidopsis

Author:

Shang Baoshuan1ORCID,Wang Lin1ORCID,Yan Xingxing1ORCID,Li Yanjun12,Li Changhao1,Wu Chaohua1,Wang Tian13,Guo Xiang4,Choi Suk Won1,Zhang Tianru1,Wang Ziying5,Tong Chun-Yip1,Oh Taerin1,Zhang Xiao4,Wang Zhiye16,Peng Xu7ORCID,Zhang Xiuren15

Affiliation:

1. Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843

2. State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Institute of Plant Virology, College of Life Sciences, Ningbo University, Ningbo 315211, China

3. College of Life Science, Shandong Normal University, Jinan, Shandong 250014, China

4. Key Laboratory of Plant Stress Biology, State Key Laboratory of Cotton Biology, School of Life Sciences, Henan University, Kaifeng 475004, China

5. Department of Biology, Texas A&M University, College Station, TX 77843

6. State Key Laboratory of Plant Physiology and Biochemistry, College of Life Sciences, Zhejiang University, Hangzhou 310058, China

7. Department of Medical Physiology, School of Medicine, Texas A&M University, Bryan, TX 77807

Abstract

Intrinsically disordered proteins (IDPs) SAID1/2 are hypothetic dentin sialophosphoprotein-like proteins, but their true functions are unknown. Here, we identified SAID1/2 as negative regulators of SERRATE (SE), a core factor in miRNA biogenesis complex (microprocessor). Loss-of-function double mutants of said1; said2 caused pleiotropic developmental defects and thousands of differentially expressed genes that partially overlapped with those in se. said1; said2 also displayed increased assembly of microprocessor and elevated accumulation of microRNAs (miRNAs). Mechanistically, SAID1/2 promote pre-mRNA processing 4 kinase A-mediated phosphorylation of SE, causing its degradation in vivo. Unexpectedly, SAID1/2 have strong binding affinity to hairpin-structured pri-miRNAs and can sequester them from SE. Moreover, SAID1/2 directly inhibit pri-miRNA processing by microprocessor in vitro. Whereas SAID1/2 did not impact SE subcellular compartmentation, the proteins themselves exhibited liquid–liquid phase condensation that is nucleated on SE. Thus, we propose that SAID1/2 reduce miRNA production through hijacking pri-miRNAs to prevent microprocessor activity while promoting SE phosphorylation and its destabilization in Arabidopsis.

Funder

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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