期刊
MOLECULAR ENDOCRINOLOGY
卷 22, 期 5, 页码 1274-1286出版社
OXFORD UNIV PRESS INC
DOI: 10.1210/me.2007-0564
关键词
-
资金
- NIDDK NIH HHS [DK33765, R01 DK033765] Funding Source: Medline
- NIEHS NIH HHS [P42 ES007381, 5 P42 ES07381, P30 ES006639, P30 ES06639] Funding Source: Medline
Hepatocyte nuclear factor (HNF)-4 alpha is a liver-enriched transcription factor that regulates numerous liver-expressed genes including several sex-specific cytochrome P450 genes. Presently, a liver-specific HNF4 alpha-deficient mouse model was used to characterize the impact of liver HNF4 alpha deficiency on a global scale using 41,174 feature microarrays. A total of 4994 HNF4 alpha-dependent genes were identified, of which about 1000 fewer genes responded to the loss of HNF4 alpha in female liver as compared with male liver. Sex differences in the impact of liver HNF4 alpha deficiency were even more dramatic when genes showing sex-specific expression were examined. Thus, 372 of the 646 sex-specific genes characterized by a dependence on HNF4 alpha responded to the loss of HNF4 alpha in males only, as compared with only 61 genes that responded in females only. Moreover, in male liver, 78% of 508 male-specific genes were down-regulated and 42% of 356 female-specific genes were up-regulated in response to the loss of HNF4 alpha, with sex specificity lost for 90% of sex-specific genes. This response to HNF4 alpha deficiency is similar to the response of male mice deficient in the GH-activated transcription factor signal transducer and activator of transcription 5b ( STAT5b), where 90% of male-specific genes were down-regulated and 61% of female-specific genes were up-regulated, suggesting these two factors cooperatively regulate liver sex specificity by mechanisms that are primarily active in males. Finally, 203 of 648 genes previously shown to bind HNF4 alpha near the transcription start site in mouse hepatocytes were affected by HNF4 alpha deficiency in mouse liver, with the HNF4 alpha-bound gene set showing a 5-fold enrichment for genes positively regulated by HNF4 alpha. Thus, a substantial fraction of the HNF4 alpha-dependent genes reported here are likely to be direct targets of HNF4 alpha.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据