Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Beyond the pol II CTD: the expanding roles of the pol II CTD modification enzymes

In plain English

AI plain-English summary

Every time a human cell reads a gene to make a protein, a molecular machine called RNA polymerase II must be switched on and off with precise chemical marks—and the enzymes that place and remove those marks are now known to have many other jobs in the cell. This matters because the current textbook picture of gene regulation is incomplete. Scientists have long known that a tail-like structure on the polymerase—the CTD—gets decorated with phosphate groups at different stages of transcription. The enzymes that add or remove those phosphates were assumed to work only on that tail. New evidence shows they also modify other proteins involved in transcription, RNA processing, and even translation. Without knowing what these enzymes actually do, researchers cannot fully understand how gene expression goes wrong in diseases such as cancer or developmental disorders. This project is fundamental science. It will use cutting-edge techniques to systematically identify all the targets of these CTD-modifying enzymes, determine what happens when their activity is lost, and map the molecular interactions that coordinate their functions. There is no immediate practical application. But similar fundamental work on transcription machinery has previously revealed targets for anticancer drugs and illuminated mechanisms behind genetic syndromes. A clearer picture of these enzymes’ full roles could eventually point toward new ways to intervene when gene expression is disrupted.

View original technical description
The multiple Tyr1Ser2Pro3Thr4Ser5Pro6Ser7 repeats within the carboxyl-terminal domain (CTD) of the large subunit of RNA polymerase II (pol II) undergo reversible phosphorylation during transcription of human protein-coding genes1. The pattern of CTD phosphorylation is controlled by CTD kinases and phosphatases through the transcription cycle, which ensures the sequential recruitment of transcription and RNA processing factors required for correct gene expression. It is now becoming clear that the "CTD" modification enzymes have multiple additional targets that may play key roles in transcription, RNA processing and even translation. The exact roles that these kinases and phosphatases play in the cell is therefore not yet well understood. The aim of the proposed research is to understand the precise role(s) that CTD kinases and phosphatases play in transcription and downstream processes through modification of the CTD and other factors, what molecular mechanisms are involved and how their activities are co-ordinated. Towards this goal, I will use state of the art technology to determine the direct effect of loss of CTD kinase or CTD phosphatase activity, identify the targets of the CTD kinases and phosphatases and characterize the molecular interactions underlying the functions of CTD kinases and phosphatases.

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Researchers

Shona Murphy (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

The roles of the human CTD phosphatases in regulating gene expression
Control, specificity and function of RNA polymerase II modification in human messenger RNA maturation
RNA Polymerase II CTD readers in gene expression regulation
The role of the pol II CTD in expression of human snRNA genes .
CTD phosphorylation and transcription termination

Original classification

Investigator Award in Science

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