Abstract
The GATA family of vertebrate DNA binding regulatory proteins are expressed in diverse tissues and at different times of development. However, the DNA binding regions of these proteins possess considerable homology and recognize a rather similar range of DNA sequence motifs. DNA binding is mediated through two domains, each containing a zinc finger. Previous results have led to the conclusion that although in some cases the N-terminal finger can contribute to specificity and strength of binding, it does not bind independently, whereas the C-terminal finger is both necessary and sufficient for binding. Here we show that although this is true for the N-terminal finger of GATA-1, those of GATA-2 and GATA-3 are capable of strong independent binding with a preference for the motif GATC. Binding requires the presence of two basic regions located on either side of the N-terminal finger. The absence of one of these near the GATA-1 N-terminal finger probably accounts for its inability to bind. The combination of a single finger and two basic regions is a new variant of a motif that has been previously found in the binding domains of other finger proteins. Our results suggest that the DNA binding properties of the N-terminal finger may help distinguish GATA-2 and GATA-3 from GATA-1 and the other GATA family members in their selective regulatory roles in vivo.
MeSH Terms
Amino Acid Sequence
Animals
Base Sequence
Binding Sites
Chickens
Cloning, Molecular
Consensus Sequence
DNA-Binding Proteins/genetics,metabolism
GATA2 Transcription Factor
GATA3 Transcription Factor
Molecular Sequence Data
Oligodeoxyribonucleotides/metabolism
Peptide Fragments/genetics,metabolism
Protein Binding
Recombinant Proteins/metabolism
Sequence Homology, Amino Acid
Titrimetry
Trans-Activators/genetics,metabolism
Transcription Factors/genetics,metabolism
Zinc Fingers
Chemicals
DNA-Binding Proteins
GATA2 Transcription Factor
GATA3 Transcription Factor
Oligodeoxyribonucleotides
Peptide Fragments
Recombinant Proteins
Trans-Activators
Transcription Factors
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Pedone P V
Laboratory of Molecular Biology, NIDDK, National Institutes of Health, Bethesda, MD 20892-0520, USA.
Omichinski J G
Nony P
Trainor C
Gronenborn A M
Clore G M
Felsenfeld G
References (25)
25 references, click to expand
-
The regulatory gene areA mediating nitrogen metabolite repression in Aspergillus nidulans. Mutations affecting specificity of gene activation alter a loop residue of a putative zinc finger.
EMBO J. 1990 May;9(5):1355-64
PMID: 1970293
-
Megakaryocytic and erythrocytic lineages share specific transcription factors.
Nature. 1990 Mar 29;344(6265):447-9
PMID: 2320113
-
Regulated expression of globin chains and the erythroid transcription factor GATA-1 during erythropoiesis in the developing mouse.
Mol Cell Biol. 1990 Dec;10(12):6596-606
PMID: 1701019
-
Erythroid differentiation in chimaeric mice blocked by a targeted mutation in the gene for transcription factor GATA-1.
Nature. 1991 Jan 17;349(6306):257-60
PMID: 1987478
-
Transcriptional activation and DNA binding by the erythroid factor GF-1/NF-E1/Eryf 1.
Genes Dev. 1990 Nov;4(11):1886-98
PMID: 2276623
-
Human transcription factor GATA-2. Evidence for regulation of preproendothelin-1 gene expression in endothelial cells.
J Biol Chem. 1992 Jan 15;267(2):1279-85
PMID: 1370462
-
GATA-binding transcription factors in hematopoietic cells.
Blood. 1992 Aug 1;80(3):575-81
PMID: 1638017
-
Expression of tal-1 and GATA-binding proteins during human hematopoiesis.
Blood. 1993 Feb 1;81(3):647-55
PMID: 7678994
-
A small single-"finger" peptide from the erythroid transcription factor GATA-1 binds specifically to DNA as a zinc or iron complex.
Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1676-80
PMID: 8446581
-
Erythroid transcription factor GATA-1 is abundantly transcribed in mouse testis.
Nature. 1993 Apr 1;362(6419):466-8
PMID: 8464479
-
DNA-binding specificity of GATA family transcription factors.
Mol Cell Biol. 1993 Jul;13(7):3999-4010
PMID: 8321207
-
DNA-binding specificities of the GATA transcription factor family.
Mol Cell Biol. 1993 Jul;13(7):4011-22
PMID: 8321208
-
NMR structure of a specific DNA complex of Zn-containing DNA binding domain of GATA-1.
Science. 1993 Jul 23;261(5120):438-46
PMID: 8332909
-
Expression of GATA-3 during lymphocyte differentiation and mouse embryogenesis.
Dev Immunol. 1992;3(1):1-11
PMID: 1343100
-
GATA-4 is a novel transcription factor expressed in endocardium of the developing heart.
Development. 1993 Jul;118(3):817-27
PMID: 8076520
-
GATA-4/5/6, a subfamily of three transcription factors transcribed in developing heart and gut.
J Biol Chem. 1994 Sep 16;269(37):23177-84
PMID: 8083222
-
Developmental stage- and spermatogenic cycle-specific expression of transcription factor GATA-1 in mouse Sertoli cells.
Development. 1994 Jul;120(7):1759-66
PMID: 7924983
-
Embryonic expression and cloning of the murine GATA-3 gene.
Development. 1994 Sep;120(9):2673-86
PMID: 7956841
-
The C-terminal zinc finger of GATA-1 or GATA-2 is sufficient to induce megakaryocytic differentiation of an early myeloid cell line.
Mol Cell Biol. 1995 Feb;15(2):634-41
PMID: 7823932
-
Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis.
Nat Genet. 1995 Sep;11(1):40-4
PMID: 7550312
-
Activity of a C. elegans GATA transcription factor, ELT-1, expressed in yeast.
J Mol Biol. 1995 Nov 10;253(5):665-76
PMID: 7473742
-
The single Cys2-His2 zinc finger domain of the GAGA protein flanked by basic residues is sufficient for high-affinity specific DNA binding.
Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2822-6
PMID: 8610125
-
The erythroid-specific transcription factor Eryf1: a new finger protein.
Cell. 1989 Sep 8;58(5):877-85
PMID: 2776214
-
Expression of an erythroid transcription factor in megakaryocytic and mast cell lineages.
Nature. 1990 Mar 29;344(6265):444-7
PMID: 2320112
-
nit-2, the major positive-acting nitrogen regulatory gene of Neurospora crassa, encodes a sequence-specific DNA-binding protein.
Proc Natl Acad Sci U S A. 1990 Jul;87(14):5331-5
PMID: 2142530