GATA-1 binding sites mapped in the β-globin locus by using mammalian chlp-chip analysis

被引:125
作者
Horak, CE
Mahajan, MC
Luscombe, NM
Gerstein, M
Weissman, SM
Snyder, M
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Genet, New Haven, CT 06520 USA
[3] Yale Univ, Dept Mol Biol & Biophys, New Haven, CT 06520 USA
关键词
D O I
10.1073/pnas.052706999
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
The expression of the p-like globin genes is intricately regulated by a series of both general and tissue-restricted transcription factors. The hemapoietic lineage-specific transcription factor GATA-1 is important for erythroid differentiation and has been implicated in regulating the expression of the erythroid-specific genes including the genes of the beta-globin locus. In the human erythroleukemic K562 cell line, only one DNA region has been identified previously as a putative site of GATA-1 interaction by in vivo footprinting studies. We mapped GATA-1 binding throughout the beta-globin locus by using chip-chip analysis of K562 cells. We found that GATA-1 binds in a region encompassing the HS2 core element, as was previously identified, and an additional region of GATA-1 binding upstream of the gammaG gene. This approach will be of general utility for mapping transcription factor binding sites within the beta-globin locus and throughout the genome.
引用
收藏
页码:2924 / 2929
页数:6
相关论文
共 24 条
[1]   CREB-binding protein cooperates with transcription factor GATA-1 and is required for erythroid differentiation [J].
Blobel, GA ;
Nakajima, T ;
Eckner, R ;
Montminy, M ;
Orkin, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (05) :2061-2066
[2]   Role of NF-Y in in vivo regulation of the γ-globin gene [J].
Duan, ZJ ;
Stamatoyannopoulos, G ;
Li, QL .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (09) :3083-3095
[3]   Looping, linking, and chromatin activity:: New insights into β-globin locus regulation [J].
Engel, JD ;
Tanimoto, K .
CELL, 2000, 100 (05) :499-502
[4]   A DEVELOPMENTALLY STABLE CHROMATIN STRUCTURE IN THE HUMAN BETA-GLOBIN GENE-CLUSTER [J].
FORRESTER, WC ;
THOMPSON, C ;
ELDER, JT ;
GROUDINE, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (05) :1359-1363
[5]   Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1 [J].
Fujiwara, Y ;
Browne, CP ;
Cunniff, K ;
Goff, SC ;
Orkin, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12355-12358
[6]   ChIP-chip: A genomic approach for identifying transcription factor binding sites [J].
Horak, CE ;
Snyder, M .
GUIDE TO YEAST GENETICS AND MOLECULAR AND CELL BIOLOGY, PT B, 2002, 350 :469-483
[7]  
Hung HL, 1999, MOL CELL BIOL, V19, P3496
[8]   INVIVO PROTEIN DNA INTERACTIONS AT THE BETA-GLOBIN GENE LOCUS [J].
IKUTA, T ;
KAN, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :10188-10192
[9]   Globin gene switching - In vivo protein-DNA interactions of the human beta-globin locus in erythroid cells expressing the fetal or the adult globin gene program [J].
Ikuta, T ;
Papayannopoulou, T ;
Stamatoyannopoulos, G ;
Kan, YW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (24) :14082-14091
[10]   Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF [J].
Iyer, VR ;
Horak, CE ;
Scafe, CS ;
Botstein, D ;
Snyder, M ;
Brown, PO .
NATURE, 2001, 409 (6819) :533-538