A GATA-1-regulated microRNA locus essential for erythropoiesis

被引:267
作者
Dore, Louis C. [1 ,2 ]
Amigo, Julio D. [3 ]
dos Santos, Camila O. [1 ,2 ]
Zhang, Zhe [4 ]
Gai, Xiaowu [4 ]
Tobias, John W. [5 ]
Yu, Duonan [1 ,2 ]
Klein, Alyssa M. [1 ,2 ]
Dorman, Christine [6 ]
Wu, Weisheng [6 ]
Hardison, Ross C. [6 ]
Paw, Barry H. [3 ]
Weiss, Mitchell J. [1 ,2 ]
机构
[1] Childrens Hosp Philadelphia, Div Hematol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Div Hematol, Boston, MA 02115 USA
[4] Childrens Hosp Philadelphia, Ctr Biomed Informat, Philadelphia, PA 19104 USA
[5] Univ Penn, Penn Bioinformat Core, Philadelphia, PA 19104 USA
[6] Penn State Univ, Dept Biochem & Mol Biol, Ctr Comparat Gen & Bioinformat, University Pk, PA 16802 USA
关键词
D O I
10.1073/pnas.0712312105
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
MicroRNAs (miRNAs) control tissue development, but their mechanism of regulation is not well understood. We used a gene complementation strategy combined with microarray screening to identify miRNAs involved in the formation of erythroid (red blood) cells. Two conserved miRNAs, miR 144 and miR 451, emerged as direct targets of the critical hematopoietic transcription factor GATA-1. In vivo, GATA-1 binds a distal upstream regulatory element to activate RNA polymerase II-mediated transcription of a single common precursor RNA (pri-miRNA) encoding both mature miRNAs. Zebrafish embryos depleted of miR 451 by using antisense morpholinos form erythroid precursors, but their development into mature circulating red blood cells is strongly and specifically impaired. These results reveal a miRNA locus that is required for erythropoiesis and uncover a new regulatory axis through which GATA-1 controls this process.
引用
收藏
页码:3333 / 3338
页数:6
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