Locus control regions of mammalian β-globin gene clusters:: combining phylogenetic analyses and experimental results to gain functional insights

被引:199
作者
Hardison, R [1 ]
Slightom, JL
Gumucio, DL
Goodman, M
Stojanovic, N
Miller, W
机构
[1] Penn State Univ, Dept Biochem & Mol Biol, Althouse Lab 206, University Pk, PA 16802 USA
[2] Penn State Univ, Ctr Gene Regulat, University Pk, PA 16802 USA
[3] Pharmacia & Upjohn Inc, Mol Biol Unit 7242, Kalamazoo, MI 49007 USA
[4] Univ Michigan, Sch Med, Dept Anat & Cell Biol, Ann Arbor, MI 48109 USA
[5] Wayne State Univ, Sch Med, Dept Anat & Cell Biol, Detroit, MI 48201 USA
[6] Penn State Univ, Dept Comp Sci & Engn, University Pk, PA 16802 USA
关键词
hemoglobin; sequence conservation; enhancement; chromatin; domain opening; DNA-binding proteins;
D O I
10.1016/S0378-1119(97)00474-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Locus control regions (LCRs) are cis-acting DNA segments needed for activation of an entire locus or gene cluster. They are operationally defined as DNA sequences needed to achieve a high level of gene expression regardless of the position of integration in transgenic mice or stably transfected cells. This review brings together the large amount of DNA sequence data from the beta-globin LCR with the vast amount of functional data obtained through the use of biochemical, cellular and transgenic experimental systems. Alignment of orthologous LCR sequences from five mammalian species locates numerous conserved regions, including previously identified cis-acting elements within the cores of nuclease hypersensitive sites (HSs) as well as conserved regions located between the HS cores. The distribution of these conserved sequences, combined with the effects of LCR fragments utilized in expression studies, shows that important sites are more widely distributed in the LCR than previously anticipated, especially in and around HS2 and HS3. We propose that the HS cores plus HS flanking DNAs comprise a 'unit' to which proteins bind and form an optimally functional structure. Multiple HS units (at least three: HS2, HS3 and HS4 cores plus flanking DNAs) together establish a chromatin structure that allows the proper developmental regulation of genes within the cluster. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:73 / 94
页数:22
相关论文
共 127 条
[1]   PARTICIPATION OF THE HUMAN BETA-GLOBIN LOCUS-CONTROL REGION IN INITIATION OF DNA-REPLICATION [J].
ALADJEM, MI ;
GROUDINE, M ;
BRODY, LL ;
DIEKEN, ES ;
FOURNIER, REK ;
WAHL, GM ;
EPNER, EM .
SCIENCE, 1995, 270 (5237) :815-819
[2]  
Armstrong JA, 1996, MOL CELL BIOL, V16, P5634
[3]   Transcriptional control of globin gene switching during vertebrate development [J].
Baron, MH .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1997, 1351 (1-2) :51-72
[4]   HUMAN GAMMA-GLOBIN TO BETA-GLOBIN GENE SWITCHING IN TRANSGENIC MICE [J].
BEHRINGER, RR ;
RYAN, TM ;
PALMITER, RD ;
BRINSTER, RL ;
TOWNES, TM .
GENES & DEVELOPMENT, 1990, 4 (03) :380-389
[5]  
BRESNICK EH, 1993, J BIOL CHEM, V268, P18824
[6]   DUAL PROMOTER ACTIVATION BY THE HUMAN BETA-GLOBIN LOCUS-CONTROL REGION [J].
BRESNICK, EH ;
FELSENFELD, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1314-1317
[7]   Synergism between hypersensitive sites confers long-range gene activation by the beta-globin locus control region [J].
Bresnick, EH ;
Tze, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (09) :4566-4571
[8]   Tetrahymena histone acetyltransferase A: A homolog to yeast Gcn5p linking histone acetylation to gene activation [J].
Brownell, JE ;
Zhou, JX ;
Ranalli, T ;
Kobayashi, R ;
Edmondson, DG ;
Roth, SY ;
Allis, CD .
CELL, 1996, 84 (06) :843-851
[9]   Synergistic regulation of human beta-globin gene switching by locus control region elements HS3 and HS4 [J].
Bungert, J ;
Dave, U ;
Lim, KC ;
Lieuw, KH ;
Shavit, JA ;
Liu, QH ;
Engel, JD .
GENES & DEVELOPMENT, 1995, 9 (24) :3083-3096
[10]   MULTIPLE ELEMENTS IN HUMAN BETA-GLOBIN LOCUS-CONTROL REGION 5' HS-2 ARE INVOLVED IN ENHANCER ACTIVITY AND POSITION-INDEPENDENT, TRANSGENE EXPRESSION [J].
CATERINA, JJ ;
CIAVATTA, DJ ;
DONZE, D ;
BEHRINGER, RR ;
TOWNES, TM .
NUCLEIC ACIDS RESEARCH, 1994, 22 (06) :1006-1011