THE MOUSE CREB (CAMP RESPONSIVE ELEMENT BINDING-PROTEIN) GENE - STRUCTURE, PROMOTER ANALYSIS, AND CHROMOSOMAL LOCALIZATION

被引:34
作者
COLE, TJ [1 ]
COPELAND, NG [1 ]
GILBERT, DJ [1 ]
JENKINS, NA [1 ]
SCHUTZ, G [1 ]
RUPPERT, S [1 ]
机构
[1] NCI,FREDERICK CANC RES & DEV CTR,ABL BASIC RES PROGRAM,MAMMALIAN GENET LAB,FREDERICK,MD 21702
关键词
D O I
10.1016/0888-7543(92)90010-P
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
In this paper we report the isolation and characterization of the mouse CREB gene. It is composed of 11 exons and 10 introns and spans a region of 70 kb. BR-A and BR-B, the two α-helical regions of the proposed basic DNA binding domain of CREB, are encoded separately on exons 10 and 11. The mouse CREB gene is expressed from a promoter that is situated in a CpG island. The promoter contains no TATA or CCAAT box homologies but has a number of putative binding sites for the acidic transcriptional activator Sp1 and a 9 11 match with the initiator region. Transcriptional start site mapping identified five major start sites spread over at least 41 nucleotides. Northern blot analysis indicated that expression of the CREB gene is almost ubiquitous with expression at differing levels of multiple transcripts. Testis expressed a predominent RNA species of approximately 1.6 kb. The CREB gene was found to be single copy in the mouse and well conserved through evolution. Finally Creb-1, the CREB locus, was mapped to the proximal region of mouse chromosome 1. © 1992.
引用
收藏
页码:974 / 982
页数:9
相关论文
共 58 条
[1]   GENETIC-ANALYSIS OF THE MOUSE USING INTERSPECIFIC CROSSES [J].
AVNER, P ;
AMAR, L ;
DANDOLO, L ;
GUENET, JL .
TRENDS IN GENETICS, 1988, 4 (01) :18-23
[2]   2 DISTINCT FORMS OF ACTIVE TRANSCRIPTION FACTOR CREB (CAMP RESPONSE ELEMENT BINDING-PROTEIN) [J].
BERKOWITZ, LA ;
GILMAN, MZ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5258-5262
[3]   CPG ISLANDS AS GENE MARKERS IN THE VERTEBRATE NUCLEUS [J].
BIRD, AP .
TRENDS IN GENETICS, 1987, 3 (12) :342-347
[4]   A CYCLIC-AMP RESPONSE ELEMENT MEDIATES REPRESSION OF TYROSINE AMINOTRANSFERASE GENE-TRANSCRIPTION BY THE TISSUE-SPECIFIC EXTINGUISHER LOCUS TSE-1 [J].
BOSHART, M ;
WEIH, F ;
SCHMIDT, A ;
FOURNIER, REK ;
SCHUTZ, G .
CELL, 1990, 61 (05) :905-916
[5]  
BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
[6]  
BUCHBERG AM, 1988, ONCOGENE RES, V2, P149
[7]   A CYCLIC AMP- AND PHORBOL ESTER-INDUCIBLE DNA ELEMENT [J].
COMB, M ;
BIRNBERG, NC ;
SEASHOLTZ, A ;
HERBERT, E ;
GOODMAN, HM .
NATURE, 1986, 323 (6086) :353-356
[8]   CHROMOSOMAL LOCATION OF MURINE AND HUMAN IL-1 RECEPTOR GENES [J].
COPELAND, NG ;
SILAN, CM ;
KINGSLEY, DM ;
JENKINS, NA ;
CANNIZZARO, LA ;
CROCE, CM ;
HUEBNER, K ;
SIMS, JE .
GENOMICS, 1991, 9 (01) :44-50
[9]   ANALYSIS OF SP1 INVIVO REVEALS MULTIPLE TRANSCRIPTIONAL DOMAINS, INCLUDING A NOVEL GLUTAMINE-RICH ACTIVATION MOTIF [J].
COUREY, AJ ;
TJIAN, R .
CELL, 1988, 55 (05) :887-898
[10]   CAMP RESPONSE ELEMENT-BINDING PROTEIN IS ACTIVATED BY CA2+/CALMODULIN-DEPENDENT AS WELL AS CAMP-DEPENDENT PROTEIN-KINASE [J].
DASH, PK ;
KARL, KA ;
COLICOS, MA ;
PRYWES, R ;
KANDEL, ER .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (11) :5061-5065