Nutrient regulation of Alternative splicing and transcription by O-GlcNAcylation

Information

  • Research Project
  • 9866679
  • ApplicationId
    9866679
  • Core Project Number
    R01GM135706
  • Full Project Number
    1R01GM135706-01
  • Serial Number
    135706
  • FOA Number
    PA-19-056
  • Sub Project Id
  • Project Start Date
    12/1/2019 - 5 years ago
  • Project End Date
    11/30/2024 - 2 months ago
  • Program Officer Name
    HOODBHOY, TANYA
  • Budget Start Date
    12/1/2019 - 5 years ago
  • Budget End Date
    11/30/2020 - 4 years ago
  • Fiscal Year
    2020
  • Support Year
    01
  • Suffix
  • Award Notice Date
    11/29/2019 - 5 years ago

Nutrient regulation of Alternative splicing and transcription by O-GlcNAcylation

The long-term goal of this project is to understand the molecular mechanisms that control gene expression and developmental transitions. While transcription has been extensively studied, the posttranscriptional mechanisms of RNA alternative splicing is much less understood despite of their importance in cellular regulation, human health, and plant growth and development. We have discovered that the Arabidopsis protein AtAcinus is evolutionarily related to but highly divergent from the human Acinus protein, which plays important roles in regulating transcription, RNA alternative splicing, and apoptosis. Our unpublished studies have shown that AtAcinus is modified by O- GlcNAcylation, plays essential role in alternative splicing of a number of genes, many of which encoding key components of signaling and developmental pathways. In particular, our data indicate that AtAcinus play important roles in regulating seed germination and flowering, two major developmental transition in plants. Using a combination of proteomics, genetics, genomic and biochemical approaches in the Arabidopsis model system, we have made tremendous progress in understanding the functions of AtAcinus. Our results support a hypothesis that AtAcinus is controlled by O-GlcNAcylation in response to endogenous and environmental cues, and in turn it regulates key cellular pathways through both transcriptional and posttranscriptional mechanisms. In this proposal, we plan to continue using the combination of proteomic, genomic and genetic approaches to further advance our understanding of Acinus regulatory pathway. We will 1) dissect the molecular functions of AtAcinus, particularly taking advantage of proximity labeling, cross-linking mass spectrometry and biochemical fractionation, CLIP-seq and CLIP-MS technologies to understand how AtAcinus carries out multiple functions (aim 1 and 3); 2) dissect how AtAcinus functions are regulated by post- translational modifications (aim 2). The experiments outlined in this proposal will greatly advance our understanding of the molecular mechanism of RNA alternatively splicing and O-GlcNAcylation and the mechanisms of signal integration at post-transcriptional level. Given the evolutionary conservation of Acinus, this study not only is important for plant biology and agriculture, but also can potentially help us understand fundamental mechanisms of signaling and cellular regulation that are relevant broadly.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    210000
  • Indirect Cost Amount
    129213
  • Total Cost
    339213
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:339213\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    CSRS
  • Study Section Name
    Cellular Signaling and Regulatory Systems Study Section
  • Organization Name
    CARNEGIE INSTITUTION OF WASHINGTON, D.C.
  • Organization Department
  • Organization DUNS
    072641707
  • Organization City
    WASHINGTON
  • Organization State
    DC
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    200051910
  • Organization District
    UNITED STATES