4.4 Article

Overlapping and distinct functions of CstF64 and CstF64τ in mammalian mRNA 3′ processing

期刊

RNA
卷 19, 期 12, 页码 1781-1790

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.042317.113

关键词

3 ' end formation; alternative polyadenylation; mRNA processing; sequencing

资金

  1. NIH [R01GM090056, R01GM088342]
  2. ACS [RSG-12-186]
  3. Edward Mallinckrodt Jr. Foundation
  4. National Center for Research Resources [5P41RR011823-17]
  5. National Institute of General Medical Sciences [8 P41 GM103533-17]
  6. National Institute on Aging [R01AG027463-04]
  7. Div Of Biological Infrastructure
  8. Direct For Biological Sciences [0846218] Funding Source: National Science Foundation

向作者/读者索取更多资源

mRNA 3' processing is dynamically regulated spatially and temporally. However, the underlying mechanisms remain poorly understood. CstF64 tau is a paralog of the general mRNA 3' processing factor, CstF64, and has been implicated in mediating testis-specific mRNA alternative polyadenylation (APA). However, the functions of CstF64 tau in mRNA 3' processing have not been systematically investigated. We carried out a comprehensive characterization of CstF64 tau and compared its properties to those of CstF64. In contrast to previous reports, we found that both CstF64 and CstF64 tau are widely expressed in mammalian tissues, and their protein levels display tissue-specific variations. We further demonstrated that CstF64 and CstF64 tau have highly similar RNA-binding specificities both in vitro and in vivo. CstF64 and CstF64 tau modulate one another's expression and play overlapping as well as distinct roles in regulating global APA profiles. Interestingly, protein interactome analyses revealed key differences between CstF64 and CstF64 tau, including their interactions with another mRNA 3' processing factor, symplekin. Together, our study of CstF64 and CstF64 tau revealed both functional overlap and specificity of these two important mRNA 3' processing factors and provided new insights into the regulatory mechanisms of mRNA 3' processing.

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