Function of GATA Factors in the Adult Mouse Liver

被引:34
|
作者
Zheng, Rena [1 ,2 ]
Rebolledo-Jaramillo, Boris [3 ]
Zong, Yiwei [4 ]
Wang, Liqing [5 ,6 ]
Russo, Pierre [7 ]
Hancock, Wayne [5 ,6 ]
Stanger, Ben Z. [4 ,8 ]
Hardison, Ross C. [9 ]
Blobel, Gerd A. [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Hematol, Philadelphia, PA 19104 USA
[3] Penn State Univ, Huck Inst Life Sci, University Pk, PA 16802 USA
[4] Univ Penn, Perelman Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
[5] Childrens Hosp Philadelphia, Div Transplant Immunol, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[6] Childrens Hosp Philadelphia, Biesecker Ctr Pediat Liver Dis, Philadelphia, PA 19104 USA
[7] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[8] Univ Penn, Perelman Sch Med, Div Gastroenterol, Dept Med,Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[9] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
来源
PLOS ONE | 2013年 / 8卷 / 12期
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR GATA-1; STEROL TRANSPORTERS ABCG5; ZINC-FINGER PROTEINS; HEART TUBE FORMATION; GENE-EXPRESSION; VENTRAL MORPHOGENESIS; RAT HEPATOCYTES; FACTOR NETWORK; FOG COFACTORS; DIFFERENTIATION;
D O I
10.1371/journal.pone.0083723
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
GATA transcription factors and their Friend of Gata (FOG) cofactors control the development of diverse tissues. GATA4 and GATA6 are essential for the expansion of the embryonic liver bud, but their expression patterns and functions in the adult liver are unclear. We characterized the expression of GATA and FOG factors in whole mouse liver and purified hepatocytes. GATA4, GATA6, and FOG1 are the most prominently expressed family members in whole liver and hepatocytes. GATA4 chromatin immunoprecipitation followed by high throughput sequencing (ChIP-seq) identified 4409 occupied sites, associated with genes enriched in ontologies related to liver function, including lipid and glucose metabolism. However, hepatocyte-specific excision of Gata4 had little impact on gross liver architecture and function, even under conditions of regenerative stress, and, despite the large number of GATA4 occupied genes, resulted in relatively few changes in gene expression. To address possible redundancy between GATA4 and GATA6, both factors were conditionally excised. Surprisingly, combined Gata4,6 loss did not exacerbate the phenotype resulting from Gata4 loss alone. This points to the presence of an unusually robust transcriptional network in adult hepatocytes that ensures the maintenance of liver function.
引用
收藏
页数:19
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