首页    期刊浏览 2024年11月29日 星期五
登录注册

文章基本信息

  • 标题:Alternative splicing of DSP1 enhances snRNA accumulation by promoting transcription termination and recycle of the processing complex
  • 本地全文:下载
  • 作者:Weili Wang ; Xuepiao Pu ; Siyu Yang
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2020
  • 卷号:117
  • 期号:33
  • 页码:20325-20333
  • DOI:10.1073/pnas.2002115117
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Small nuclear RNAs (snRNAs) are the basal components of the spliceosome and play crucial roles in splicing. Their biogenesis is spatiotemporally regulated. However, related mechanisms are still poorly understood. Defective in snRNA processing (DSP1) is an essential component of the DSP1 complex that catalyzes plant snRNA 3′-end maturation by cotranscriptional endonucleolytic cleavage of the primary snRNA transcripts (presnRNAs). Here, we show that DSP1 is subjected to alternative splicing in pollens and embryos, resulting in two splicing variants, DSP1 α and DSP1 β. Unlike DSP1α, DSP1β is not required for presnRNA 3′-end cleavage. Rather, it competes with DSP1α for the interaction with CPSF73-I, the catalytic subunit of the DSP1 complex, which promotes efficient release of CPSF73-I and the DNA-dependent RNA polymerease II (Pol II) from the 3′ end of snRNA loci thereby facilitates snRNA transcription termination, resulting in increased snRNA levels in pollens. Taken together, this study uncovers a mechanism that spatially regulates snRNA accumulation.
  • 关键词:snRNA ; transcript termination ; DSP1 ; alternative splicing ; DSP1α
国家哲学社会科学文献中心版权所有