INVIVO PROTEIN DNA INTERACTIONS AT THE BETA-GLOBIN GENE LOCUS

被引:89
作者
IKUTA, T [1 ]
KAN, YW [1 ]
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT LAB MED,SAN FRANCISCO,CA 94143
关键词
DIMETHYL SULFATE; INVIVO FOOTPRINTING; K562; CELLS; HELA CELLS; LYMPHOCYTE-B;
D O I
10.1073/pnas.88.22.10188
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
We have investigated in vivo protein-DNA interactions in the beta-globin gene locus by dimethyl sulfate (DMS) footprinting in K562 cells, which express epsilon- and gamma-globin but not beta-globin. In the locus control region, hypersensitive site 2 (HS-2) exhibited footprints in several putative protein binding motifs. HS-3 was not footprinted. The beta-promoter was also not footprinted, while extensive footprints were observed in the promoter of the active gamma-globin gene. No footprints were seen in the (A)gamma and beta-3' enhancers. With several motifs, additional protein interactions and alterations in binding patterns occurred with hemin induction. In HeLa cells, some footprints were observed in some of the motifs in HS-2, compatible with the finding that HS-2 has some enhancer function in HeLa cells, albeit much weaker than its activity in K562 cells. No footprint was seen in B lymphocytes. In vivo footprinting is a useful method for studying relevant protein-DNA interactions in erythroid cells.
引用
收藏
页码:10188 / 10192
页数:5
相关论文
共 33 条
[1]   INVIVO PROTEIN DNA INTERACTIONS IN A GLUCOCORTICOID RESPONSE ELEMENT REQUIRE THE PRESENCE OF THE HORMONE [J].
BECKER, PB ;
GLOSS, B ;
SCHMID, W ;
STRAHLE, U ;
SCHUTZ, G .
NATURE, 1986, 324 (6098) :686-688
[2]   GENOMIC FOOTPRINTING REVEALS CELL TYPE SPECIFIC DNA-BINDING OF UBIQUITOUS FACTORS [J].
BECKER, PB ;
RUPPERT, S ;
SCHUTZ, G .
CELL, 1987, 51 (03) :435-443
[3]   AN ENHANCER ELEMENT LIES 3' TO THE HUMAN A-GAMMA-GLOBIN GENE [J].
BODINE, DM ;
LEY, TJ .
EMBO JOURNAL, 1987, 6 (10) :2997-3004
[4]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[5]   HUMAN BETA-GLOBIN GENE-EXPRESSION IN TRANSGENIC MICE IS ENHANCED BY A DISTANT DNASE-I HYPERSENSITIVE SITE [J].
CURTIN, PT ;
LIU, DP ;
LIU, W ;
CHANG, JC ;
KAN, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (18) :7082-7086
[6]   THE HUMAN BETA-GLOBIN PROMOTER - NUCLEAR-PROTEIN FACTORS AND ERYTHROID SPECIFIC INDUCTION OF TRANSCRIPTION [J].
DEBOER, E ;
ANTONIOU, M ;
MIGNOTTE, V ;
WALL, L ;
GROSVELD, F .
EMBO JOURNAL, 1988, 7 (13) :4203-4212
[7]   B-LINEAGE SPECIFIC INTERACTIONS OF AN IMMUNOGLOBULIN ENHANCER WITH CELLULAR FACTORS INVIVO [J].
EPHRUSSI, A ;
CHURCH, GM ;
TONEGAWA, S ;
GILBERT, W .
SCIENCE, 1985, 227 (4683) :134-140
[8]   MOLECULAR ANALYSIS OF THE HUMAN BETA-GLOBIN LOCUS ACTIVATION REGION [J].
FORRESTER, WC ;
NOVAK, U ;
GELINAS, R ;
GROUDINE, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (14) :5439-5443
[9]   INVIVO FOOTPRINTING OF MHC CLASS-II GENES - BARE PROMOTERS IN THE BARE LYMPHOCYTE SYNDROME [J].
KARA, CJ ;
GLIMCHER, LH .
SCIENCE, 1991, 252 (5006) :709-712
[10]   HUMAN CHRONIC MYELOGENOUS LEUKEMIA CELL-LINE WITH POSITIVE PHILADELPHIA CHROMOSOME [J].
LOZZIO, CB ;
LOZZIO, BB .
BLOOD, 1975, 45 (03) :321-334