Role of poly(ADP-ribose) polymerase 1 in regulating RNA polymerase II elongation and mRNA splicing

Information

  • NSF Award
  • 2230470
Owner
  • Award Id
    2230470
  • Award Effective Date
    1/15/2022 - 3 years ago
  • Award Expiration Date
    7/31/2023 - a year ago
  • Award Amount
    $ 581,272.00
  • Award Instrument
    Standard Grant

Role of poly(ADP-ribose) polymerase 1 in regulating RNA polymerase II elongation and mRNA splicing

PARP1 (poly-ADP-ribose polymerase), a chromatin-binding protein, is crucial for maintaining genomic integrity in mammals through regulation of proliferation, differentiation and aging. Control of gene expression occurs at different levels – importantly, at transcription initiation and mRNA splicing. Recent studies show that transcription and splicing are co-regulated and that chromatin structure plays a key role in this process. In an earlier study, the research group found that PARP1, which is well known for DNA repair, also regulates alternative splicing. This project aims to understand how PARP1-chromatin complex coordinates RNA polymerase II (RNAPII) elongation, RNA, and splicing factors to regulate co-transcriptional splicing. The outcomes will provide insights into PARP1 function, especially in RNA biogenesis. The project will offer training opportunities for underrepresented high school and undergraduate students during summer months. Outreach activities will include mentoring graduate students at local and regional small colleges, as well as early career faculty at US minority-serving institutions as part of a unique University of Kentucky mentoring program. <br/><br/>Mechanistic details of how PARP1 regulates co-transcriptional splicing are lacking. This research project will test the hypotheses that PARP1 regulates co-transcriptional splicing in two non-mutually exclusive ways: i) by acting as an adapter to recruit splicing factors to RNA; and/or ii) by modulating chromatin structure in ways that affect RNAPII elongation and kinetics. Large-scale genomics and gene-specific approaches will be applied to map the genetic and biochemical interactions of PARP1-RNA-chromatin. These studies will provide significant new knowledge about this newly identified activity of PARP1 in alternative splicing. Furthermore, deciphering the mechanism(s) by which PARP1 modulates chromatin to regulate alternative splicing and RNA processing will provide fundamental insights into the complex role of chromatin structure in eukaryotic gene regulation.<br/><br/>This project is jointly funded by the Genetic Mechanisms program in the Molecular and Cellular Biosciences Division of the Biological Sciences Directorate and the Established Program to Stimulate Competitive Research (EPSCoR).<br/><br/>This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

  • Program Officer
    Arcady Mushegianamushegi@nsf.gov7032928528
  • Min Amd Letter Date
    6/22/2022 - 2 years ago
  • Max Amd Letter Date
    6/22/2022 - 2 years ago
  • ARRA Amount

Institutions

  • Name
    Van Andel Research Institute
  • City
    Grand Rapids
  • State
    MI
  • Country
    United States
  • Address
    333 Bostwick Ave NE
  • Postal Code
    495032518
  • Phone Number
    6162345750

Investigators

  • First Name
    Yvonne
  • Last Name
    Fondufe-Mittendorf
  • Email Address
    y.FondufeMittendorf@vai.org
  • Start Date
    6/22/2022 12:00:00 AM

Program Element

  • Text
    Genetic Mechanisms
  • Code
    1112
  • Text
    EPSCoR Co-Funding
  • Code
    9150

Program Reference

  • Text
    NANOSCALE BIO CORE
  • Code
    7465
  • Text
    RAHSS
  • Code
    7744
  • Text
    EXP PROG TO STIM COMP RES
  • Code
    9150
  • Text
    REU SUPP-Res Exp for Ugrd Supp
  • Code
    9251