Deletions within the mouse β-globin locus control region preferentially reduce βmin globin gene expression

被引:8
|
作者
Alami, R
Bender, MA
Feng, YQ
Fiering, SN
Hug, BA
Ley, TJ
Groudine, M
Bouhassira, EE
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Med, Div Hematol, Bronx, NY 10461 USA
[2] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[3] Univ Washington, Sch Med, Dept Pediat, Seattle, WA 98195 USA
[4] Univ Washington, Sch Med, Dept Radiat Oncol, Seattle, WA 98195 USA
[5] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Microbiol, Hanover, NH 03755 USA
[6] Washington Univ, Sch Med, Dept Med, Div Bone Marrow Transplantat & Stem Cell Biol, St Louis, MO 63110 USA
[7] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
关键词
D O I
10.1006/geno.1999.6104
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The mouse beta-globin gene cluster is regulated, at least in part, by a locus control region (LCR) composed of several developmentally stable DNase I hypersensitive sites located upstream of the genes. In this report, we examine the level of expression of the beta(min) and beta(maj) genes in adult mice in which HS2, HS3, or HS5,6 has been either deleted or replaced by a selectable marker via homologous recombination in ES cells. Primer extension analysis of PNA extracted from circulating reticulocytes and HPLC analysis of globin chains from peripheral red blood cells revealed that all mutations that reduce the overall output of the locus preferentially decrease beta(min) expression over beta(maj). The implications of these findings for the mechanism by which the LCR controls expression of the beta(maj) and beta(min) promoters are discussed. (C) 2000 Academic Press.
引用
收藏
页码:417 / 424
页数:8
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