SICKLE modulates lateral root development by promoting degradation of lariat intronic RNA

Author:

Wu Chengyun123ORCID,Wang Xiaoqing1,Zhen Weibo1ORCID,Nie Yaqing14ORCID,Li Yan1ORCID,Yuan Penglai14ORCID,Liu Qiaoqiao1ORCID,Guo Siyi1ORCID,Shen Zhenguo4ORCID,Zheng Binglian5ORCID,Hu Zhubing123ORCID

Affiliation:

1. State Key Laboratory of Crop Stress Adaptation and Improvement, School of Life Sciences, Henan University , Kaifeng 475004, China

2. Academy for Advanced Interdisciplinary Studies, Henan University , Kaifeng 475004, China

3. Sanya Institute of Henan University , Sanya 572025, China

4. College of Life Sciences, Nanjing Agricultural University , Nanjing 210095, China

5. State Key Laboratory of Genetic Engineering, Ministry of Education Key Laboratory of Biodiversity Sciences and Ecological Engineering, Institute of Plant Biology, School of Life Sciences, Fudan University , Shanghai 200438, China

Abstract

Abstract Plant lateral roots (LRs) play vital roles in anchorage and uptake of water and nutrients. Here, we reveal that degradation of lariat intronic RNAs (lariRNAs) modulated by SICKLE (SIC) is required for LR development in Arabidopsis (Arabidopsis thaliana). Loss of SIC results in hyper-accumulation of lariRNAs and restricts the outgrowth of LR primordia, thereby reducing the number of emerged LRs. Decreasing accumulation of lariRNAs by over-expressing RNA debranching enzyme 1 (DBR1), a rate-limiting enzyme of lariRNA decay, restored LR defects in SIC-deficient plants. Mechanistically, SIC interacts with DBR1 and facilitates its nuclear accumulation, which is achieved through two functionally redundant regions (SIC1–244 and SIC252–319) for nuclear localization. Of the remaining amino acids in this region, six (SIC245–251) comprise a DBR1-interacting region while two (SICM246 and SICW251) are essential for DBR1–SIC interaction. Reducing lariRNAs restored microRNA (miRNA) levels and LR development in lariRNA hyper-accumulating plants, suggesting that these well-known regulators of LR development mainly function downstream of lariRNAs. Taken together, we propose that SIC acts as an enhancer of DBR1 nuclear accumulation by driving nuclear localization through direct interaction, thereby promoting lariRNA decay to fine-tune miRNA biogenesis and modulating LR development.

Funder

National Natural Science Foundation of China

Outstanding Youth Foundation of Henan Province

Programs for Team and Talents of Innovative Research (in Science and Technology) in Henan Province

Foundation of Henan Educational Committee

111 Project

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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