The human bone morphogenetic protein 4 (BMP-4) gene: Molecular structure and transcriptional regulation

被引:44
作者
Shore, EM
Xu, MQ
Shah, PB
Janoff, HB
Hahn, GV
Deardorff, MA
Sovinsky, L
Spinner, NB
Zasloff, MA
Wozney, JM
Kaplan, FS
机构
[1] Univ Penn, Sch Med, Dept Orthopaed Surg, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Div Human Genet & Mol Biol, Philadelphia, PA 19104 USA
[5] Genet Inst, Cambridge, MA 02140 USA
关键词
bone morphogenetic protein 4; gene structure; gene organization; transcriptional regulation;
D O I
10.1007/s002239900518
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bone morphogenetic protein 4 (BMP-4) is a vital regulatory molecule that functions throughout human development in mesoderm induction, tooth development, limb formation, bone induction, and fracture repair and is overexpressed in patients who have fibrodysplasia ossificans progressiva. The human gene encoding bone morphogenetic protein 4 (BMP-4) has been isolated and its structural organization characterized. The complete DNA sequence of an 11.2 kb region has been determined. BMP-4 mRNA is transcribed from four exons, although there is evidence that alternate first exons may be used. Transcript initiation occurs at variable positions within a GA-rich region of the DNA, The promoter region is CC-rich with no obvious TATA or CAAT consensus sequences, and contains both positive and negative transcriptional regulatory elements within the 3 kb 5' flanking region of the RNA start site. Comparison of the human and murine BMP-4 genes reveals highly conserved sequences not only in the exon-coding regions but also within the introns and 5' flanking regions. BMP-4 localizes to human chromosome 14q21 by fluorescence in situ hybridization, a location more centromeric than that recently reported. These studies provide a foundation for understanding the genetic regulation of this important gene in human development.
引用
收藏
页码:221 / 229
页数:9
相关论文
共 48 条
[1]   Transcriptional activation of hedgehog target genes in Drosophila is mediated directly by the cubitus interruptus protein, a member of the GLI family of zinc finger DNA-binding proteins [J].
Alexandre, C ;
Jacinto, A ;
Ingham, PW .
GENES & DEVELOPMENT, 1996, 10 (16) :2003-2013
[2]  
Ausubel F.M., 1992, SHORT PROTOCOLS MOL, V2nd
[3]   A signaling pathway to translational control [J].
Brown, EJ ;
Schreiber, SL .
CELL, 1996, 86 (04) :517-520
[4]   DIRECT REGULATION OF DECAPENTAPLEGIC BY ULTRABITHORAX AND ITS ROLE IN DROSOPHILA MIDGUT MORPHOGENESIS [J].
CAPOVILLA, M ;
BRANDT, M ;
BOTAS, J .
CELL, 1994, 76 (03) :461-475
[5]   CLONING AND SEQUENCE OF BONE MORPHOGENETIC PROTEIN-4 CDNA FROM FETAL-RAT CALVARIAL CELL [J].
CHEN, D ;
FENG, JQ ;
FENG, M ;
HARRIS, MA ;
MUNDY, GR ;
HARRIS, SE .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1174 (03) :289-292
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]  
Conaway, 1994, TRANSCRIPTION MECHAN, P63
[8]   CHROMOSOMAL LOCALIZATION OF 7 MEMBERS OF THE MURINE TGF-BETA SUPERFAMILY SUGGESTS CLOSE LINKAGE TO SEVERAL MORPHOGENETIC MUTANT LOCI [J].
DICKINSON, ME ;
KOBRIN, MS ;
SILAN, CM ;
KINGSLEY, DM ;
JUSTICE, MJ ;
MILLER, DA ;
CECI, JD ;
LOCK, LF ;
LEE, A ;
BUCHBERG, AM ;
SIRACUSA, LD ;
LYONS, KM ;
DERYNCK, R ;
HOGAN, BLM ;
COPELAND, NG ;
JENKINS, NA .
GENOMICS, 1990, 6 (03) :505-520
[9]   PROMOTERS FOR HOUSEKEEPING GENES [J].
DYNAN, WS .
TRENDS IN GENETICS, 1986, 2 (08) :196-197
[10]   COMPILATION OF VERTEBRATE-ENCODED TRANSCRIPTION FACTORS [J].
FAISST, S ;
MEYER, S .
NUCLEIC ACIDS RESEARCH, 1992, 20 (01) :3-26