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BCL6 suppression of BCL2 via Miz1 and its disruption in diffuse large B cell lymphoma.


ABSTRACT: The BCL6 proto-oncogene encodes a transcriptional repressor that is required for germinal center (GC) formation and whose deregulation by genomic lesions is implicated in the pathogenesis of GC-derived diffuse large B cell lymphoma (DLBCL) and, less frequently, follicular lymphoma (FL). The biological function of BCL6 is only partially understood because no more than a few genes have been functionally characterized as direct targets of BCL6 transrepression activity. Here we report that the anti-apoptotic proto-oncogene BCL2 is a direct target of BCL6 in GC B cells. BCL6 binds to the BCL2 promoter region by interacting with the transcriptional activator Miz1 and suppresses Miz1-induced activation of BCL2 expression. BCL6-mediated suppression of BCL2 is lost in FL and DLBCL, where the 2 proteins are pathologically coexpressed, because of BCL2 chromosomal translocations and other mechanisms, including Miz1 deregulation and somatic mutations in the BCL2 promoter region. These results identify an important function for BCL6 in facilitating apoptosis of GC B cells via suppression of BCL2, and suggest that blocking this pathway is critical for lymphomagenesis.

SUBMITTER: Saito M 

PROVIDER: S-EPMC2708681 | biostudies-literature | 2009 Jul

REPOSITORIES: biostudies-literature

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BCL6 suppression of BCL2 via Miz1 and its disruption in diffuse large B cell lymphoma.

Saito Masumichi M   Novak Urban U   Piovan Erich E   Basso Katia K   Sumazin Pavel P   Schneider Christof C   Crespo Marta M   Shen Qiong Q   Bhagat Govind G   Califano Andrea A   Chadburn Amy A   Pasqualucci Laura L   Dalla-Favera Riccardo R  

Proceedings of the National Academy of Sciences of the United States of America 20090623 27


The BCL6 proto-oncogene encodes a transcriptional repressor that is required for germinal center (GC) formation and whose deregulation by genomic lesions is implicated in the pathogenesis of GC-derived diffuse large B cell lymphoma (DLBCL) and, less frequently, follicular lymphoma (FL). The biological function of BCL6 is only partially understood because no more than a few genes have been functionally characterized as direct targets of BCL6 transrepression activity. Here we report that the anti-  ...[more]

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