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Repression of the PDCD2 gene by BCL6 and the implications for the pathogenesis of human B and T cell lymphomas
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The human
BCL6
gene on chromosome 3 band q27, which encodes a transcriptional repressor, is implicated in the pathogenesis of human lymphomas, especially the diffuse large B-cell type. We previously identified the human
PDCD2
(programmed cell death-2) gene as a target of BCL6 repression.
PDCD2
encodes a protein that is expressed in many human tissues, including lymphocytes, and is known to interact with corepressor complexes. We now show that BCL6 can bind directly to the
PDCD2
promoter, repressing its transcription. Knockdown of endogenous BCL6 in a human B cell lymphoma line by introduction of small interfering RNA duplexes increases PDCD2 protein expression. Furthermore, there is an inverse relationship between the expression levels of the BCL6 and PDCD2 proteins in the lymphoid tissues of mice overexpressing human BCL6 (high BCL6 levels, minimal PDCD2) and controls (minimal BCL6, high PDCD2) as well as in tissues examined from some human B and T cell lymphomas. These data confirm
PDCD2
as a target of BCL6 and support the concept that repression of
PDCD2
by BCL6 is likely important in the pathogenesis of certain human lymphomas.
Title: Repression of the
PDCD2
gene by BCL6 and the implications for the pathogenesis of human B and T cell lymphomas
Description:
The human
BCL6
gene on chromosome 3 band q27, which encodes a transcriptional repressor, is implicated in the pathogenesis of human lymphomas, especially the diffuse large B-cell type.
We previously identified the human
PDCD2
(programmed cell death-2) gene as a target of BCL6 repression.
PDCD2
encodes a protein that is expressed in many human tissues, including lymphocytes, and is known to interact with corepressor complexes.
We now show that BCL6 can bind directly to the
PDCD2
promoter, repressing its transcription.
Knockdown of endogenous BCL6 in a human B cell lymphoma line by introduction of small interfering RNA duplexes increases PDCD2 protein expression.
Furthermore, there is an inverse relationship between the expression levels of the BCL6 and PDCD2 proteins in the lymphoid tissues of mice overexpressing human BCL6 (high BCL6 levels, minimal PDCD2) and controls (minimal BCL6, high PDCD2) as well as in tissues examined from some human B and T cell lymphomas.
These data confirm
PDCD2
as a target of BCL6 and support the concept that repression of
PDCD2
by BCL6 is likely important in the pathogenesis of certain human lymphomas.
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