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Grant: Project Grant

Institut de recherches cliniques de Montréal

$933,300.00

A Multi-scale Mechanism for the RNAPII CTD

FY 2023-24

Summary
For a gene to "express" itself and contribute to the function of the cell that hosts it, it first needs to be transcribed. Gene transcription consists of making a copy of the gene as an RNA molecule. This RNA molecule is then translated into a protein. The enzyme that generates RNAs from genes coding for proteins is called RNA polymerase II (RNAPII). This enzyme contains a peculiar domain called CTD, made of several repetitions of a small amino acid chain. The CTD is essential for cell viability and is evolutionarily conserved. Two decades of research taught us that the CTD serves as a docking platform for several proteins to join RNAPII during the transcription of genes, a process notably important for the transcribed RNA to become competent to be translated. More recently, several research groups have proposed different roles for the CTD. According to these studies, the CTD, rather than docking proteins, would rather make "hit and run" interactions with other CTD molecules and other proteins, creating zones in the cell nucleus where RNAPII is found in high concentrations, which would then favor more efficient transcription of the neighboring genes. These more recent models are radically different from the traditional view of CTD function. Our preliminary results investigating this dichotomy prompt us to propose that both models are co-existing. We propose that this is made possible by the repetitive nature of the CTD and that different segments of the CTD are dedicated to different aspects of its function.
Program
Project Grant
Location
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
500823
Name
Robert François
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - B
Projecttitle
A Multi-scale Mechanism for the RNAPII CTD
Programtype2
Operating Grants
Orgnameinp2
Institut de recherches cliniques de Montréal
Cihramount2
$933,300
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
C-Terminal Domain (Ctd); Intrinsically Disordered Regions; Low Complexity Domains; Rna Polymerase Ii; Transcription
Abstract
For a gene to "express" itself and contribute to the function of the cell that hosts it, it first needs to be transcribed. Gene transcription consists of making a copy of the gene as an RNA molecule. This RNA molecule is then translated into a protein. The enzyme that generates RNAs from genes coding for proteins is called RNA polymerase II (RNAPII). This enzyme contains a peculiar domain called CTD, made of several repetitions of a small amino acid chain. The CTD is essential for cell viability and is evolutionarily conserved. Two decades of research taught us that the CTD serves as a docking platform for several proteins to join RNAPII during the transcription of genes, a process notably important for the transcribed RNA to become competent to be translated. More recently, several research groups have proposed different roles for the CTD. According to these studies, the CTD, rather than docking proteins, would rather make "hit and run" interactions with other CTD molecules and other proteins, creating zones in the cell nucleus where RNAPII is found in high concentrations, which would then favor more efficient transcription of the neighboring genes. These more recent models are radically different from the traditional view of CTD function. Our preliminary results investigating this dichotomy prompt us to propose that both models are co-existing. We propose that this is made possible by the repetitive nature of the CTD and that different segments of the CTD are dedicated to different aspects of its function.
Competitiondate
202403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Robert, François
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $933,300~ $0~
Institut de recherches cliniques de Montréal - $933,3… | Canada Spends