STRUCTURAL CHARACTERIZATION AND ALTERNATE SPLICING OF THE GENE ENCODING THE PREADIPOCYTE EGF-LIKE PROTEIN PREF-1

被引:101
作者
SMAS, CM [1 ]
GREEN, D [1 ]
SUL, HS [1 ]
机构
[1] HARVARD UNIV, SCH PUBL HLTH, DEPT NUTR, BOSTON, MA 02115 USA
关键词
D O I
10.1021/bi00197a029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Preadipocyte factor 1 (pref-1), a member of the EGF-like protein family, is a transmembrane protein with six tandem EGF-like repeats in the putative extracellular domain. Expression of pref-1 is abolished during the in vitro differentiation of 3T3-L1 preadipocytes to adipocytes, and constitutive expression of pref-1 in preadipocytes inhibits their differentiation [Smas, C. M., and Sul, H. S. (1993) Cell 73, 725-734]. In the present studies, we have isolated and characterized genomic clones for pref-1 and have identified multiple pref-1 transcripts generated by alternate splicing. The pref-1 gene consists of five exons and four introns spanning approximately 7.3 kb. By primer extension analysis, the transcription start site was determined to be 169 bp upstream from the translation initiation codon. We have identified functional promoter sequences by transient transfection using a 2.1 kb fragment of the pref-1 5' flanking region linked to a luciferase gene; the pref-1-luciferase fusion gene construct gave 20-fold higher promoter activity as compared to the promoterless vector. Analysis of exon-intron junctions reveals that unlike the majority of the mammalian EGF-like genes, EGF-like repeats of pref-1 are not encoded by discrete exons. Through RT-PCR and the isolation and analysis of multiple pref-1 cDNA clones, we have identified, in addition to full-length pref-1, five alternately spliced forms with various in-frame deletions of all or a part of the sixth EGF-like repeat, juxtamembrane, and predicted transmembrane domains. We conclude, by comparing cDNA and genomic sequences, that all of the multiple forms of pref-1 transcript have in-frame deletions generated by alternate splicing within exon 5.
引用
收藏
页码:9257 / 9265
页数:9
相关论文
共 56 条
[1]   GENERATION OF PROTEIN ISOFORM DIVERSITY BY ALTERNATIVE SPLICING - MECHANISTIC AND BIOLOGICAL IMPLICATIONS [J].
ANDREADIS, A ;
GALLEGO, ME ;
NADALGINARD, B .
ANNUAL REVIEW OF CELL BIOLOGY, 1987, 3 :207-242
[2]   THE GENE STRUCTURE OF HUMAN ANTI-HEMOPHILIC FACTOR-IX [J].
ANSON, DS ;
CHOO, KH ;
REES, DJG ;
GIANNELLI, F ;
GOULD, K ;
HUDDLESTON, JA ;
BROWNLEE, GG .
EMBO JOURNAL, 1984, 3 (05) :1053-1060
[3]  
ARATANI Y, 1988, J BIOL CHEM, V263, P16163
[4]  
BALDWIN CT, 1989, J BIOL CHEM, V264, P15747
[5]   HUMAN EPIDERMAL GROWTH-FACTOR PRECURSOR - CDNA SEQUENCE, EXPRESSION INVITRO AND GENE ORGANIZATION [J].
BELL, GI ;
FONG, NM ;
STEMPIEN, MM ;
WORMSTED, MA ;
CAPUT, D ;
KU, L ;
URDEA, MS ;
RALL, LB ;
SANCHEZPESCADOR, R .
NUCLEIC ACIDS RESEARCH, 1986, 14 (21) :8427-8446
[6]   CHARACTERIZATION OF THE RAT TRANSFORMING GROWTH FACTOR-ALPHA GENE AND IDENTIFICATION OF PROMOTER SEQUENCES [J].
BLASBAND, AJ ;
ROGERS, KT ;
AZIZKHAN, JC ;
LEE, DC .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (05) :2111-2121
[7]  
BRASIER AR, 1989, BIOTECHNIQUES, V7, P1116
[8]   COMPILATION AND ANALYSIS OF EUKARYOTIC POL-II PROMOTER SEQUENCES [J].
BUCHER, P ;
TRIFONOV, EN .
NUCLEIC ACIDS RESEARCH, 1986, 14 (24) :10009-10026
[9]  
CALVO JC, 1991, J BIOL CHEM, V266, P11237
[10]  
CARPENTER G, 1990, J BIOL CHEM, V265, P7709