The KRAB-containing zinc-finger transcriptional regulator ZBRK1 activates SCA2 gene transcription through direct interaction with its gene product, ataxin-2

被引:34
|
作者
Hallen, Linda [1 ,2 ]
Klein, Holger [1 ]
Stoschek, Carola [1 ]
Wehrmeyer, Silke [1 ]
Nonhoff, Ute [1 ]
Ralser, Markus [1 ]
Wilde, Jeannine [1 ]
Roehr, Christina [1 ,2 ]
Schweiger, Michal R. [1 ]
Zatloukal, Kurt [3 ]
Vingron, Martin [1 ]
Lehrach, Hans [1 ]
Konthur, Zoltan [1 ]
Krobitsch, Sylvia [1 ]
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Free Univ Berlin, Dept Biol Chem & Pharm, D-14195 Berlin, Germany
[3] Med Univ Graz, A-8036 Graz, Austria
关键词
DNA-DAMAGE; EXPRESSION; BRCA1; REPRESSION; PROTEINS; COMPLEX; CARCINOMAS; APOPTOSIS; PATHWAY; DISEASE;
D O I
10.1093/hmg/ddq436
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
Gene transcription is controlled by transcriptional regulators acting with specific co-regulators to allow gene activation and repression. Here, we report the identification of the KRAB-containing zinc-finger transcriptional regulator, ZBRK1, as an interaction partner of the SCA2 gene product ataxin-2. Furthermore, we discovered that an elevated ZBRK1 level resulted in increased ataxin-2 levels, whereas interference on transcriptional and protein levels of ZBRK1 yielded reduced ataxin-2 levels, suggesting that a complex comprising ZBRK1 and ataxin-2 regulates SCA2 gene transcription. A bioinformatic analysis utilizing the known ZBRK1 consensus DNA-binding motif revealed ZBRK1-binding sites in the SCA2 promoter. These predicted sites were experimentally validated by chromatin-immunoprecipitation experiments along with luciferase-based promoter analyses corroborating that SCA2 gene transcription is controlled by a ZBRK1/ataxin-2 complex. Finally, we demonstrate that SCA2 gene transcription is significantly reduced in colon tumors possessing low ZBRK1 transcripts. Thus, our results provide first evidence that ataxin-2 acts as a co-regulator of ZBRK1 activating its own transcription, thereby representing the first identified ZBRK1 co-activator.
引用
收藏
页码:104 / 114
页数:11
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