Characterization of HRG22, a human homologue of the putative tumor suppressor gene HIC1

被引:29
作者
Deltour, S [1 ]
Pinte, S [1 ]
Guérardel, C [1 ]
Leprince, D [1 ]
机构
[1] Inst Pasteur, Inst Biol, CNRS, UMR 8526, F-59017 Lille, France
关键词
HIC1; HIC-1; CtBP; BTB/POZ; C2H2 zinc finger; 17p13.3; 22q11.2; transcriptional repression; HDACs;
D O I
10.1006/bbrc.2001.5624
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Database searches identified on chromosome 22q11.2, a region subject to translocations, an homologue of the HIC1 (hypermethylated in cancer) candidate tumor suppressor gene located at 17p13.3. This gene was termed HRG22 for HIC1-related gene on chromosome 22. We have characterized a new HRG22 upstream coding exon and defined the complete coding sequence of the human and zebrafish HRG22 genes. Alignment of the HRG22 and HIC1 proteins from various species revealed high sequence homology in their N-terminal BTB/POZ and five C-terminal C2H2 zinc finger domains and highlighted a conserved GLDLSKK/R peptide in their middle region. The full-length HRG22 and HIC1 proteins colocalize onto nuclear dots and share several functional properties since their BTB/POZ domains heterodimerize and are autonomous transcriptional repression domain insensitive to Trichostatin A, a histone deacetylase (HDAC) inhibitor. Thus, HIC1 and HRG22 define a subgroup of BTB/POZ domains unable to recruit repressing complexes containing an HDAC activity. (C) 2001 Academic Press.
引用
收藏
页码:427 / 434
页数:8
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