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  • 标题:Identification of BERP (brain-expressed RING finger protein) as a p53 target gene that modulates seizure susceptibility through interacting with GABAA receptors
  • 本地全文:下载
  • 作者:Carol C. Cheung ; Caimei Yang ; Thorsten Berger
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2010
  • 卷号:107
  • 期号:26
  • 页码:11883-11888
  • DOI:10.1073/pnas.1006529107
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:p53 is a central player in responses to cellular stresses and a major tumor suppressor. The identification of unique molecules within the p53 signaling network can reveal functions of this important transcription factor. Here, we show that brain-expressed RING finger protein (BERP) is a gene whose expression is up-regulated in a p53-dependent manner in human cells and in mice. We generated BERP-deficient mice by gene targeting and demonstrated that they exhibit increased resistance to pentylenetetrazol-induced seizures. Electrophysiological and biochemical studies of cultured cortical neurons of BERP-deficient mice showed a decrease in the amplitude of GABAA receptor (GABAAR)-mediated miniature inhibitory postsynaptic currents as well as reduced surface protein expression of GABAARs containing the {gamma}2-subunit. However, BERP deficiency did not decrease GABAAR{gamma}2 mRNA levels, raising the possibility that BERP may act at a posttranscriptional level to regulate the intracellular trafficking of GABAARs. Our results indicate that BERP is a unique p53-regulated gene and suggest a role for p53 within the central nervous system.
  • 关键词:brat ; neurotransmitter ; brain ; RNF22 ; TRIM3
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