Characterization of the rat, mouse, and human genes of growth/differentiation factor-15/macrophage inhibiting cytokine-1 (GDF-15/MIC-1)

被引:133
作者
Böttner, M
Laaff, M
Schechinger, B
Rappold, G
Unsicker, K
Suter-Crazzolara, C
机构
[1] Univ Heidelberg, Dept Neuroanat, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Dept Human Genet, D-69120 Heidelberg, Germany
关键词
gene structure; mRNA expression; promoter; transforming growth factor-beta;
D O I
10.1016/S0378-1119(99)00309-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We have isolated the rat, mouse and human genes of a distant member of the TGF-beta superfamily, growth/differentiation factor-15/macrophage inhibiting cytokine-l (GDF-15/MIC-1) by screening of genomic libraries. All three genes are composed of two exons, and contain one single intron that interrupts the coding sequences at identical positions within the prepro-domain of the corresponding proteins. The predicted proteins contain the structural hallmarks of members of the TGF-beta superfamily, including the seven conserved carboxy-terminal cysteine residues that form the cystine knot. The orthologous molecules show the lowest sequence conservation of all members of the TGF-beta superfamily. RT-PCR reveals an abundant expression of GDF-15/MIC-1 mRNA in numerous embryonic and adult organs and tissues. Promoter analysis of the rat promoter indicates the presence of multiple regulatory elements, including a TATA-like sequence as well as several SP1, AP-1 and AP-2 sites. Deletion analysis suggests that a 350 bp region upstream of the start of the open reading frame appears to be the most important for regulation of transcription. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 111
页数:7
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