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
[11]   BOTH THE BASIC REGION AND THE LEUCINE ZIPPER DOMAIN OF THE CYCLIC-AMP RESPONSE ELEMENT BINDING (CREB) PROTEIN ARE ESSENTIAL FOR TRANSCRIPTIONAL ACTIVATION [J].
DWARKI, VJ ;
MONTMINY, M ;
VERMA, IM .
EMBO JOURNAL, 1990, 9 (01) :225-232
[12]   MULTIPLE SEQUENCE ELEMENTS IN THE C-FOS PROMOTER MEDIATE INDUCTION BY CAMP [J].
FISCH, TM ;
PRYWES, R ;
SIMON, MC ;
ROEDER, RG .
GENES & DEVELOPMENT, 1989, 3 (02) :198-211
[13]   DEVELOPMENTAL SWITCH OF CREM - FUNCTION DURING SPERMATOGENESIS - FROM ANTAGONIST TO ACTIVATOR [J].
FOULKES, NS ;
MELLSTROM, B ;
BENUSIGLIO, E ;
SASSONECORSI, P .
NATURE, 1992, 355 (6355) :80-84
[14]   CREM GENE - USE OF ALTERNATIVE DNA-BINDING DOMAINS GENERATES MULTIPLE ANTAGONISTS OF CAMP-INDUCED TRANSCRIPTION [J].
FOULKES, NS ;
BORRELLI, E ;
SASSONECORSI, P .
CELL, 1991, 64 (04) :739-749
[15]   LOCALIZATION OF THE MUSCLE, LIVER, AND BRAIN GLYCOGEN-PHOSPHORYLASE GENES ON LINKAGE MAPS OF MOUSE CHROMOSOME-19, CHROMOSOME-12, AND CHROMOSOME-2, RESPECTIVELY [J].
GLASER, T ;
MATTHEWS, KE ;
HUDSON, JW ;
SETH, P ;
HOUSMAN, DE ;
CRERAR, MM .
GENOMICS, 1989, 5 (03) :510-521
[16]   CHARACTERIZATION OF MOTIFS WHICH ARE CRITICAL FOR ACTIVITY OF THE CYCLIC AMP-RESPONSIVE TRANSCRIPTION FACTOR CREB [J].
GONZALEZ, GA ;
MENZEL, P ;
LEONARD, J ;
FISCHER, WH ;
MONTMINY, MR .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) :1306-1312
[17]   CYCLIC-AMP STIMULATES SOMATOSTATIN GENE-TRANSCRIPTION BY PHOSPHORYLATION OF CREB AT SERINE-133 [J].
GONZALEZ, GA ;
MONTMINY, MR .
CELL, 1989, 59 (04) :675-680
[18]  
Green EL, 1981, GENETICS PROBABILITY, P77
[19]   CYCLIC-AMP - RESPONSIVE DNA-BINDING PROTEIN - STRUCTURE BASED ON A CLONED PLACENTAL CDNA [J].
HOEFFLER, JP ;
MEYER, TE ;
YUN, Y ;
JAMESON, JL ;
HABENER, JF .
SCIENCE, 1988, 242 (4884) :1430-1433
[20]   THE GENE FOR THE UBIQUITOUS OCTAMER-BINDING PROTEIN OCT-1 IS ON HUMAN CHROMOSOME-1, REGION CEN-Q32, AND NEAR LY-22 AND LTW-4 ON MOUSE CHROMOSOME-1 [J].
HSIEH, CL ;
STURM, R ;
HERR, W ;
FRANCKE, U .
GENOMICS, 1990, 6 (04) :666-672