Coronin 2B deficiency induces nucleolar stress and neuronal apoptosis

Author:

Chen Yu1,Wu Hongjiao1,Yang Yujie1,Yi Wanying1,Qiu Yue2,Ma Shuangshuang2,Xu Jinying3,Fan Yingying1,Chen Yuewen1

Affiliation:

1. Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences

2. HKUST Shenzhen Research Institute

3. henzhen Institute of Advanced Technology, Chinese Academy of Sciences

Abstract

Abstract

The nucleolus is the critical non-membranous organelle within nuclei, which responsible for ribosomal DNA (rDNA) transcription and ribosome biogenesis in eukaryotes. The transcription of rDNA, a rate-limiting step for ribosome biogenesis, is tightly regulated to meet the demand for global protein synthesis in response to cell physiology, especially in neurons, which undergo rapid changes in morphology and protein composition during development and synaptic plasticity. However, it is unknown how the pre-initiation complex for rDNA transcription is efficiently assembled within the nucleolus of neurons. Here, we report that the nucleolar protein coronin 2B regulates rDNA transcription and maintains nucleolar function through direct interaction with upstream binding factor (UBF), an activator of RNA polymerase I transcriptional machinery. We show that coronin 2B knockdown impairs the formation of the transcription initiation complex, inhibits rDNA transcription, destroys nucleolar integrity, and ultimately induces nucleolar stress. In turn, coronin 2B-mediated nucleolar stress leads to p53 stabilization and activation, eventually resulting in neuronal apoptosis. Thus, we identified that coronin 2B coordinates with UBF to regulate rDNA transcription and maintain proper nucleolar function in neurons.

Publisher

Research Square Platform LLC

Reference56 articles.

1. Emerging roles of the neuronal nucleolus;Hetman M;Trends Neurosci,2012

2. Targeting the nucleolus as a therapeutic strategy in human disease;Corman A;Trends Biochem Sci,2023

3. Regulation of RNA Polymerase I Transcription in Development, Disease, and Aging;Sharifi S;Annu Rev Biochem,2018

4. Basic mechanisms in RNA polymerase I transcription of the ribosomal RNA genes;Goodfellow SJ;J Biol Chem,2013

5. The RNA polymerase I transcription machinery: an emerging target for the treatment of cancer;Drygin D;Annu Rev Pharmacol,2010

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3