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Maf1, a new player in the regulation of human RNA polymerase III transcription.


ABSTRACT:

Background

Human RNA polymerase III (pol III) transcription is regulated by several factors, including the tumor suppressors P53 and Rb, and the proto-oncogene c-Myc. In yeast, which lacks these proteins, a central regulator of pol III transcription, called Maf1, has been described. Maf1 is required for repression of pol III transcription in response to several signal transduction pathways and is broadly conserved in eukaryotes.

Methodology/principal findings

We show that human endogenous Maf1 can be co-immunoprecipitated with pol III and associates in vitro with two pol III subunits, the largest subunit RPC1 and the alpha-like subunit RPAC2. Maf1 represses pol III transcription in vitro and in vivo and is required for maximal pol III repression after exposure to MMS or rapamycin, treatments that both lead to Maf1 dephosphorylation.

Conclusions/significance

These data suggest that Maf1 is a major regulator of pol III transcription in human cells.

SUBMITTER: Reina JH 

PROVIDER: S-EPMC1762419 | biostudies-literature | 2006 Dec

REPOSITORIES: biostudies-literature

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Publications

Maf1, a new player in the regulation of human RNA polymerase III transcription.

Reina Jaime H JH   Azzouz Teldja N TN   Hernandez Nouria N  

PloS one 20061227


<h4>Background</h4>Human RNA polymerase III (pol III) transcription is regulated by several factors, including the tumor suppressors P53 and Rb, and the proto-oncogene c-Myc. In yeast, which lacks these proteins, a central regulator of pol III transcription, called Maf1, has been described. Maf1 is required for repression of pol III transcription in response to several signal transduction pathways and is broadly conserved in eukaryotes.<h4>Methodology/principal findings</h4>We show that human en  ...[more]

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