HNF-1β Regulates Transcription of the PKD Modifier Gene Kif12

被引:48
作者
Gong, Yimei [1 ]
Ma, Zhendong [1 ]
Patel, Vishal [1 ]
Fischer, Evelyne [3 ]
Hiesberger, Thomas [1 ]
Pontoglio, Marco [3 ]
Igarashi, Peter [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
[3] Inst Pasteur, Dept Dev Biol, CNRS, Gene Express Dev & Dis Lab,URA 2578, Paris, France
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2009年 / 20卷 / 01期
基金
美国国家卫生研究院;
关键词
POLYCYSTIC KIDNEY-DISEASE; NUCLEAR; EXPRESSION; MUTATIONS; HNF1; PROTEIN; MOUSE; VHNF1;
D O I
10.1681/ASN.2008020238
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Hepatocyte nuclear factor-1 beta (HNF-1 beta) is a transcription factor that regulates gene expression in the kidney, liver, pancreas, and other epithelial organs. Mutations of HNF-1 beta lead to a syndrome of inherited renal cysts and diabetes and are also a common cause of sporadic renal dysplasia. The full complement of target genes responsible for the functions of HNF-1 beta, however, is incompletely defined. Using a functional genomics approach involving chromatin immunoprecipitation and promoter arrays, combined with gene expression profiling, we found that an HNF-1 beta target gene in the kidney is kinesin family member 12 (Kif12), a gene previously identified as a candidate modifier gene in the cpk mouse model of polycystic kidney disease. Mutations of HNF-1 beta inhibited Kif12 transcription in both cultured cells and knockout mice by altering co-factor recruitment and histone modification. Because kinesin-12 family members participate in orienting cell division, downregulation of Kif12 may underlie the abnormal planar cell polarity observed in cystic kidney diseases.
引用
收藏
页码:41 / 47
页数:7
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