CHROMOSOMAL LOCALIZATION OF 7 MEMBERS OF THE MURINE TGF-BETA SUPERFAMILY SUGGESTS CLOSE LINKAGE TO SEVERAL MORPHOGENETIC MUTANT LOCI

被引:130
作者
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
机构
[1] VANDERBILT UNIV, MED CTR, SCH MED, DEPT CELL BIOL, NASHVILLE, TN 37232 USA
[2] GENENTECH INC, DEPT DEV BIOL, S SAN FRANCISCO, CA 94080 USA
[3] NCI, FREDERICK CANC RES FACIL,BIONET RES INC, BASIC RES PROGRAM,MAMMALIAN GENET LAB, FREDERICK, MD 21701 USA
[4] GENENTECH INC, DEPT MOLEC BIOL, S SAN FRANCISCO, CA 94080 USA
关键词
D O I
10.1016/0888-7543(90)90480-I
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chromosomal locations have been assigned to seven members of the TGF-β superfamily using an interspecific mouse backcross. Probes for the Tgfb-1, -2, and -3, Bmp-2a and -3, and Vgr-1 genes recognized only single loci, whereas the Bmp-2b probe recognized two independently segregating loci (designated Bmp-2b1 and Bmp-2b2). The results show that the seven members of the TGF-β superfamily map to eight different chromosomes, indicating that the TGF-β family has become widely dispersed during evolution. Five of the eight loci (Tgfb-1, Bmp-2a, Bmp-2b1, Bmp-2b2, Vgr-1) mapped near mutant loci associated with connective tissue and skeletal disorders, raising the possibility that at least some of these mutations result from defects in TGF-β-related genes. © 1990.
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页码:505 / 520
页数:16
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