共 1 条
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.
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页码:104 / 114
页数:11
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