Functional analysis and chromosomal mapping of Gata5, a gene encoding a zinc finger DNA-binding protein

被引:35
作者
Nemer, G
Qureshi, ST
Malo, D
Nemer, M
机构
[1] Clin Res Inst Montreal, Lab Dev & Differenciat Cardiaq, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Dept Pharmacol, Montreal, PQ H3C 3J7, Canada
[3] McGill Univ, Dept Med & Human Genet, Montreal, PQ H3G 1Y6, Canada
[4] L11 144 Montreal Gen Hosp, Ctr Study Host Resistance, Montreal, PQ H3G 1A4, Canada
关键词
D O I
10.1007/s003359901146
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 GATA family of zinc finger proteins are transcriptional regulators with critical functions in lineage differentiation and embryonic development. Based on structural and expression pattern comparisons, the GATA proteins have been subdivided into two groups. The first subgroup consists of GATA-1, -2, and 3, which are all highly expressed in the hematopoietic system, whereas GATA-4, -5, and -6 are present essentially in the heart and gut. We have isolated and functionally characterized the rat GATA-5 cDNA, which encodes a 45-kDa protein with 71%, 73%, and 97% homology to its amphibian, avian, and murine homologs, respectively. Northern blot analysis showed that rat GATA-5 is expressed in a dynamic pattern during embryonic and postnatal development. In the midgestation embryo, GATA-5 transcripts are most abundant in the heart and decrease dramatically in the postnatal heart; in contrast, GATA-5 expression is upregulated in the lung and gut during postnatal development. Functional studies with recombinant GATA-4, -5, and -6 proteins show that GATA-5 has preferential affinity for a subset of GATA elements found on cardiac promoters and differentially activate cardiac gene transcription. Structure-function analysis revealed the presence of an activation domain within the carboxy terminal region of GATA-5 that is essential for transcriptional regulation of target promoters. Linkage analysis localized Gata5 to distal mouse Chromosome (Chr) 2 in a conserved linkage group with genes localized to rat Chr 3q43 and human Chr 20q13.2-q13.3. The results suggest that GATA-5 may have specific downstream targets and that GATA-4, -5, and -6 can only partially substitute for each other in cardiogenesis. Thus, Gata5 probably plays a specialized evolutionary conserved role in cardiac development.
引用
收藏
页码:993 / 999
页数:7
相关论文
共 35 条
[1]   Expression of NK-2 class homeobox gene Nkx2-6 in foregut endoderm and heart [J].
Biben, C ;
Hatzistavrou, T ;
Harvey, RP .
MECHANISMS OF DEVELOPMENT, 1998, 73 (01) :125-127
[2]  
Bristow J, 1995, CELL MOL BIOL RES, V41, P307
[3]   TENASCIN-X - A NOVEL EXTRACELLULAR-MATRIX PROTEIN ENCODED BY THE HUMAN XB GENE OVERLAPPING P450C21B [J].
BRISTOW, J ;
TEE, MK ;
GITELMAN, SE ;
MELLON, SH ;
MILLER, WL .
JOURNAL OF CELL BIOLOGY, 1993, 122 (01) :265-278
[4]   Chick NKx-2.3 represents a novel family member of vertebrate homologues to the Drosophila homeobox gene tinman: Differential expression of cNKx-2.3 and cNK-2.5 during heart and gut development [J].
Buchberger, A ;
Pabst, O ;
Brand, T ;
Seidl, K ;
Arnold, HH .
MECHANISMS OF DEVELOPMENT, 1996, 56 (1-2) :151-163
[5]   EXPRESSION OF HOMEOBOX GENES MSX-1 (HOX-7) AND MSX-2 (HOX-8) DURING CARDIAC DEVELOPMENT IN THE CHICK [J].
CHANTHOMAS, PS ;
THOMPSON, RP ;
ROBERT, B ;
YACOUB, MH ;
BARTON, PJR .
DEVELOPMENTAL DYNAMICS, 1993, 197 (03) :203-216
[6]  
Charron F, 1999, MOL CELL BIOL, V19, P4355
[7]   Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum [J].
de la Pompa, JL ;
Timmerman, LA ;
Takimoto, H ;
Yoshida, H ;
Elia, AJ ;
Samper, E ;
Potter, J ;
Wakeham, A ;
Marengere, L ;
Langille, BL ;
Crabtree, GR ;
Mak, TW .
NATURE, 1998, 392 (6672) :182-186
[8]   The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors [J].
Durocher, D ;
Charron, F ;
Schwartz, RJ ;
Warren, R ;
Nemer, M .
EMBO JOURNAL, 1997, 16 (18) :5687-5696
[9]   MOLECULAR REGULATION OF ATRIOVENTRICULAR VALVULOSEPTAL MORPHOGENESIS [J].
EISENBERG, LM ;
MARKWALD, RR .
CIRCULATION RESEARCH, 1995, 77 (01) :1-6
[10]  
Grepin C, 1997, DEVELOPMENT, V124, P2387