THE COMPLETE SEQUENCE AND PROMOTER ACTIVITY OF THE HUMAN A-RAF-1 GENE (ARAF1)

被引:16
作者
LEE, JE
BECK, TW
BRENNSCHEIDT, U
DEGENNARO, LJ
RAPP, UR
机构
[1] NCI,FREDERICK CANC RES & DEV CTR,VIRAL CARCINOGENESIS LAB,FREDERICK,MD 21702
[2] NCI,FREDERICK CANC RES & DEV CTR,PROGRAM RESOURCES INC DYNCORP,FREDERICK,MD 21702
[3] GEORGE WASHINGTON UNIV,DEPT GENET,WASHINGTON,DC
[4] UNIV MASSACHUSETTS,SCH MED,DEPT NEUROL,WORCESTER,MA 01655
[5] UNIV MASSACHUSETTS,SCH MED,DEPT CELL BIOL,WORCESTER,MA 01655
关键词
D O I
10.1006/geno.1994.1125
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 raf proto-oncogenes encode cytoplasmic protein serine/threonine kinases, which play a critical role in cell growth and development. One of these, A-raf-1 (human gene symbol, ARAF1), which is predominantly expressed in mouse urogenital tissues, has been mapped to an evolutionarily conserved linkage group composed of ARAF1, SYN1, TIMP, and properdin located at human chromosome Xp11.2. We have isolated human genomic DNA clones containing the expressed gene (ARAF1) on the X chromosome and a pseudogene (ARAF2) on chromosome 7p12-q11.21. Analysis of the nucleotide sequence from the ARAF1 genomic clones demonstrated that it consists of 16 exons encoded by minimally 10,776 nucleotides. The major transcriptional start site (+1) was determined by RNase protection and primer extension assays. Promoter activity was confirmed by functional assays using DNA fragments fused to a CAT reporter gene. The ARAF1 minimal promoter, located between nucleotides -59 and +93, has a low G + C content and lacks consensus TATA and Inr sequences but shows sequence similarity at position -1 to the E box that is known to interact with USF and TFII-I transcription factors. (C) 1994 Academic Press, Inc.
引用
收藏
页码:43 / 55
页数:13
相关论文
共 64 条
[1]  
AELST LV, 1993, P NATL ACAD SCI USA, V90, P6213
[2]   REQUIREMENT OF THE DROSOPHILA RAF HOMOLOG FOR TORSO FUNCTION [J].
AMBROSIO, L ;
MAHOWALD, AP ;
PERRIMON, N .
NATURE, 1989, 342 (6247) :288-291
[3]   THE COMPLETE CODING SEQUENCE OF THE HUMAN A-RAF-1 ONCOGENE AND TRANSFORMING ACTIVITY OF A HUMAN A-RAF CARRYING RETROVIRUS [J].
BECK, TW ;
HULEIHEL, M ;
GUNNELL, M ;
BONNER, TI ;
RAPP, UR .
NUCLEIC ACIDS RESEARCH, 1987, 15 (02) :595-609
[4]   MOLECULAR-ORGANIZATION OF THE HUMAN RAF-1 PROMOTER REGION [J].
BECK, TW ;
BRENNSCHEIDT, U ;
SITHANANDAM, G ;
CLEVELAND, J ;
RAPP, UR .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (07) :3325-3333
[5]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[6]   STRUCTURE AND BIOLOGICAL-ACTIVITY OF HUMAN HOMOLOGS OF THE RAF MIL ONCOGENE [J].
BONNER, TI ;
KERBY, SB ;
SUTRAVE, P ;
GUNNELL, MA ;
MARK, G ;
RAPP, UR .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (06) :1400-1407
[7]   THE COMPLETE CODING SEQUENCE OF THE HUMAN RAF ONCOGENE AND THE CORRESPONDING STRUCTURE OF THE C-RAF-1 GENE [J].
BONNER, TI ;
OPPERMANN, H ;
SEEBURG, P ;
KERBY, SB ;
GUNNELL, MA ;
YOUNG, AC ;
RAPP, UR .
NUCLEIC ACIDS RESEARCH, 1986, 14 (02) :1009-1015
[8]   X-CHROMOSOME INACTIVATION OF THE HUMAN TIMP GENE [J].
BROWN, CJ ;
FLENNIKEN, AM ;
WILLIAMS, BRG ;
WILLARD, HF .
NUCLEIC ACIDS RESEARCH, 1990, 18 (14) :4191-4195
[9]   SERUM-INDUCED, TPA-INDUCED, AND RAS-INDUCED EXPRESSION FROM AP-1/ETS-DRIVEN PROMOTERS REQUIRES RAF-1 KINASE [J].
BRUDER, JT ;
HEIDECKER, G ;
RAPP, UR .
GENES & DEVELOPMENT, 1992, 6 (04) :545-556
[10]  
COLEMAN M, 1990, AM J HUM GENET, V47, P935