Please use this identifier to cite or link to this item: https://doi.org/10.1073/pnas.0605562104
Title: BLIMP1 regulates cell growth through repression of p53 transcription
Authors: Yan, J.
Jiang, J.
Ching, A.L.
Wu, Q.
Ng, H.-H. 
Chin, K.-C.
Keywords: Apoptosis
Growth arrest
Transcription regulation
Issue Date: 6-Feb-2007
Citation: Yan, J., Jiang, J., Ching, A.L., Wu, Q., Ng, H.-H., Chin, K.-C. (2007-02-06). BLIMP1 regulates cell growth through repression of p53 transcription. Proceedings of the National Academy of Sciences of the United States of America 104 (6) : 1841-1846. ScholarBank@NUS Repository. https://doi.org/10.1073/pnas.0605562104
Abstract: Tight regulation of p53 is essential for maintaining normal cell growth. Here we report that BLIMP1 acts in an autoregulatory feedback loop that controls p53 activity through repression of p53 transcription. p53 binds to and positively regulates BL1MP1, which encodes for a known B cell transcriptional repressor. Knockdown of BLIMP1 by siRNA results in both apoptosis and growth arrest in human colon cancer cells and cell-cycle arrest in primary human fibroblasts. Interestingly, the levels of both p53 mRNA and protein are substantially increased after BLIMP1 depletion, which is accompanied by the induction of p53 target genes. Importantly, the apoptosis induced by BLIMP1 depletion in HCT116 cells is largely abrogated in cells lacking p53 or in cells depleted in p53 by siRNA. We further demonstrate that BLIMP1 binds to the p53 promoter and represses p53 transcription, and this provides a mechanistic explanation for the induction of p53 response in cells depleted of BLIMP1. Hence, suppression of p53 transcription is a crucial function of endogenous BLIMP1 and is essential for normal cell growth. © 2007 by The National Academy of Sciences of the USA.
Source Title: Proceedings of the National Academy of Sciences of the United States of America
URI: http://scholarbank.nus.edu.sg/handle/10635/100182
ISSN: 00278424
DOI: 10.1073/pnas.0605562104
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