The C-terminal domain of RNA polymerase II (CTD) is a unique structure in eukaryotes that coordinates various transcriptional factors to Pol II through its post-translational modifications. The simple consensus sequence of CTD (Y1S2P3T4S5P6S7) is repeated many times consecutively and is mostly conserved. The phosphorylation of the two SP motifs in the sequence has been identified to be essential for every round of transcription but the other three residues, Y1, T4 and S7, also have functional implications during transcription. To understand the molecular mechanism of these post-translational modifications of CTD on transcription modulation, we combine a novel mass spectrometry methodology with biochemical and biophysical studies to investigate how the identity and modification states of these three positions affect the post-translational modification states of RNA polymerase II. We will then examine the consequences of altering the modification patterns of CTD on transcription, which will allow us to understand this fundamental mechanism that regulates transcription.

Public Health Relevance

The C-terminal domain of RNA polymerase II (CTD) orchestrates the eukaryotic transcription process through its post-translational modification, namely CTD code. Malfunction of enzymes that alter the CTD phosphorylation state can lead to cell death, developmental defects and cancer. In this proposal, we will decipher the fundamental mechanisms of how the CTD governs transcription by identifying the sites of modifications using an innovative mass spectrometry strategy. We will identify the factors that determine the ?CTD code? generated. The reconstruction of the generation of CTD code in vitro will be correlated to transcription processes in vivo and give us a comprehensive understanding of this fundamental process in biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM125882-02
Application #
9751900
Study Section
Macromolecular Structure and Function B Study Section (MSFB)
Program Officer
Adkins, Ronald
Project Start
2018-08-01
Project End
2022-05-31
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Texas Austin
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78759