CHROMOSOMAL MAPPING OF THE HUMAN (MACS) AND MOUSE (MACS) GENES ENCODING THE MARCKS PROTEIN

被引:26
作者
BLACKSHEAR, PJ
TUTTLE, JS
OAKEY, RJ
SELDIN, MF
CHERY, M
PHILIPPE, C
STUMPO, DJ
机构
[1] DUKE UNIV,MED CTR,DEPT MED,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT BIOCHEM,DURHAM,NC 27710
[3] DUKE UNIV,MED CTR,DIV ENDOCRINOL METAB & NUTR,DURHAM,NC 27710
[4] CTR REG TRANSFUS SANGUINE NANCY BRABOIS,GENET LAB,VANDOEVRE LES NANCY,FRANCE
[5] DUKE UNIV,MED CTR,DEPT MICROBIOL,DURHAM,NC 27710
关键词
D O I
10.1016/S0888-7543(05)80300-3
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
The myristoylated, alanine-rich C-kinase substrate, or MARCKS protein, is a major cellular substrate for protein kinase C that is also a high-affinity calmodulin-binding protein. In addition, it is the prototype of a small family of myristoylated, calmodulin-binding protein kinase C substrate proteins. We isolated a phage clone from a mouse genomic library that spanned the entire coding sequence of the mouse MARCKS protein. The first 612 bp of the putative promoter was 89% identical to a corresponding region of the human promoter, and contained at least 59 potential transcription factor binding sites in analogous locations; both human and mouse promoters lacked TATA boxes. The mouse genomic probe was used to localize the mouse gene to chromosome 10, in the middle of a linkage group that corresponds to a region on human chromosome 6q. These data strongly suggested that the human gene would localize to 6q21. This was confirmed by studies of DNA from a patient with del(6)(q21), in which expression of the human gene encoding MARCKS, MACS, was only about 50% of normal; MARCKS mRNA expression in lymphoblast RNA from this patient was only 22% of normal. These studies confirm that the mouse and human MARCKS proteins are products of the same genes in their respective species; differences in their primary sequence can therefore be attributed to species variation rather than to the existence of related genes. © 1992 Academic Press, Inc. All rights reserved.
引用
收藏
页码:168 / 174
页数:7
相关论文
共 35 条
[1]  
BACKSHEAR PJ, 1992, J BIOL CHEM, V267, P13540
[2]  
BISHOP D T, 1985, Genetic Epidemiology, V2, P349, DOI 10.1002/gepi.1370020404
[3]   PROTEIN-KINASE-C ACTIVATION POTENTLY DOWN-REGULATES THE EXPRESSION OF ITS MAJOR SUBSTRATE, 80K, IN SWISS 3T3-CELLS [J].
BROOKS, SF ;
HERGET, T ;
ERUSALIMSKY, JD ;
ROZENGURT, E .
EMBO JOURNAL, 1991, 10 (09) :2497-2505
[4]   STRUCTURAL ORGANIZATION OF THE MOUSE PROTO-MYB GENE [J].
CASTLE, S ;
SHEINESS, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 132 (02) :688-695
[5]  
CHERY M, 1989, ANN GENET-PARIS, V32, P82
[6]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[7]   NUMBER AND EVOLUTIONARY CONSERVATION OF ALPHA-TUBULIN AND BETA-TUBULIN AND CYTOPLASMIC BETA-ACTIN AND GAMMA-ACTIN GENES USING SPECIFIC CLONED CDNA PROBES [J].
CLEVELAND, DW ;
LOPATA, MA ;
MACDONALD, RJ ;
COWAN, NJ ;
RUTTER, WJ ;
KIRSCHNER, MW .
CELL, 1980, 20 (01) :95-105
[8]  
COOKE M P, 1989, New Biologist, V1, P66
[9]   REGULATION OF T-CELL RECEPTOR SIGNALING BY A SRC FAMILY PROTEIN-TYROSINE KINASE (P59FYN) [J].
COOKE, MP ;
ABRAHAM, KM ;
FORBUSH, KA ;
PERLMUTTER, RM .
CELL, 1991, 65 (02) :281-291
[10]  
ERUSALIMSKY JD, 1991, J BIOL CHEM, V266, P7073