The N-terminal zinc finger of the erythroid transcription factor GATA-1 binds GATC motifs in DNA

被引:79
作者
Newton, A [1 ]
Mackay, J [1 ]
Crossley, M [1 ]
机构
[1] Univ Sydney, Dept Biochem, Sydney, NSW 2006, Australia
关键词
D O I
10.1074/jbc.M106256200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian transcription factor GATA-1 is required for normal erythroid and megakaryocytic development. GATA-1 contains two zinc fingers, the C-terminal finger, which is known to bind (A/T)GATA(A/G) motifs in DNA and the N-finger, which is important for interacting with co-regulatory proteins such as Friend of GATA (FOG). We now show that, like the C-finger, the N-finger of GATA-1 is also capable of binding DNA but recognizes distinct sequences with the core GATC. We demonstrate that the GATA-1 N-finger can bind these sequences in vitro and that in cellular assays, GATA-1 can activate promoters containing GATC motifs. Experiments with mutant GATA-1 proteins confirm the importance of the N-finger, as the C-finger is not required for transactivation from GATC sites. Recently four naturally occurring mutations in GATA-1 have been shown to be associated with familial blood disorders. These mutations all map to the N-finger domain. We have investigated the effect of these mutations on the recognition of GATC sites by the N-finger and show that one mutation R216Q abolishes DNA binding, whereas the others have only minor effects.
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收藏
页码:35794 / 35801
页数:8
相关论文
共 38 条
[1]   A SWI/SNF-related chromatin remodeling complex, E-RC1, is required for tissue-specific transcriptional regulation by EKLF in vitro [J].
Armstrong, JA ;
Bieker, JJ ;
Emerson, BM .
CELL, 1998, 95 (01) :93-104
[2]   A SINGLE POINT MUTATION IS THE CAUSE OF THE GREEK FORM OF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN [J].
BERRY, M ;
GROSVELD, F ;
DILLON, N .
NATURE, 1992, 358 (6386) :499-502
[3]   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
[4]   Use of altered specificity mutants to probe a specific protein-protein interaction in differentiation:: The GATA-1:FOG complex [J].
Crispino, JD ;
Lodish, MB ;
MacKay, JP ;
Orkin, SH .
MOLECULAR CELL, 1999, 3 (02) :219-228
[5]  
CROSSLEY M, 1995, MOL CELL BIOL, V15, P2448
[6]  
DRACHMAN JG, 2001, IN PRESS BLOOD
[7]   Key residues characteristic of GATA N-fingers are recognized by FOG [J].
Fox, AH ;
Kowalski, K ;
King, GF ;
Mackay, JP ;
Crossley, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (50) :33595-33603
[8]   Transcriptional cofactors of the FOG family interact with GATA proteins by means of multiple zinc fingers [J].
Fox, AH ;
Liew, C ;
Holmes, M ;
Kowalski, K ;
Mackay, J ;
Crossley, M .
EMBO JOURNAL, 1999, 18 (10) :2812-2822
[9]   Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation [J].
Freson, K ;
Devriendt, K ;
Matthijs, G ;
Van Hoof, A ;
De Vos, R ;
Thys, C ;
Minner, K ;
Hoylaerts, MF ;
Vermylen, J ;
Van Geet, C .
BLOOD, 2001, 98 (01) :85-92
[10]   Transcriptional activity of Pannier is regulated negatively by heterodimerization of the GATA DNA-binding domain with a cofactor encoded by the u-shaped gene of Drosophila [J].
Haenlin, M ;
Cubadda, Y ;
Blondeau, F ;
Heitzler, P ;
Lutz, Y ;
Simpson, P ;
Ramain, P .
GENES & DEVELOPMENT, 1997, 11 (22) :3096-3108