Cloning and Functional Characterization of The Regulation Region of Human BRD7 Gene
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This work was supported by grants from Key Program of The National Natural Science Foundation of China (30330560), The National Natural Science Foundation of China (30300175, 30400238, 30400528) and Natural Science Foundation of Hunan Province (05JJ300063).

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    Abstract:

    BRD7, a novel bromodomain gene, has been cloned by cDNA RDA (cDNA Representational Difference Analysis). The GenBank accession number is AF152604. Previous studies showed that BRD7 gene was down-regulated in nasopharyngeal carcinoma (NPC) cells and tissues. Over expression of BRD7 in NPC cells can inhibit cell proliferation and cell cycle progression from G1 to S phase, and can partly inhibit the aberrant growth of NPC cells. In order to explore the molecular mechanisms that involved in the down-regulation of BRD7 gene in NPC cells, bioinformatic approaches were adopted and a putative promoter region was found. The luciferase expression vectors containing BRD7 promoter region were further constructed . Transient transfection results suggested that the analyzed sequence contained BRD7 promoter. Transcriptional factor Sp1 is responsive to this region. Inhibition of the Sp1 binding to BRD7 promoter by mithramycin A significantly reduced the promoter activity and the endogenous expression of BRD7 in mRNA level.

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Liu Hua-Ying, Luo Xiao-Min, Niu Zhao-Xia, Peng Cong, Li Gui-Yuan, Zhou Ming, Zhou Yan-Hong, Li Xiao-Ling, Li Wei-Song, Xiang Bo. Cloning and Functional Characterization of The Regulation Region of Human BRD7 Gene[J]. Progress in Biochemistry and Biophysics,2006,33(6):531-539

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History
  • Received:December 20,2005
  • Revised:February 15,2006
  • Accepted:
  • Online: June 14,2006
  • Published: June 20,2006