Characterization of the gene EPAC2:: Structure, chromosomal localization, tissue expression, and identification of the liver-specific isoform

被引:53
作者
Ueno, H
Shibasaki, T
Iwanaga, T
Takahashi, K
Yokoyama, Y
Liu, LM
Yokoi, N
Ozaki, N
Matsukura, S
Yano, H
Seino, S
机构
[1] Chiba Univ, Grad Sch Med, Dept Cellular & Mol Med, Chuo Ku, Chiba 2608670, Japan
[2] Hokkaido Univ, Grad Sch Vet Med, Lab Anat, Sapporo, Hokkaido 0600818, Japan
[3] Chiba Univ, Grad Sch Med, Dept Mol Immunol, CREST,Chuo Ku, Chiba 2608670, Japan
[4] Okayama Univ, Sch Med, Dept Pediat, Okayama 7008558, Japan
[5] Chiba Univ, Sch Med, Dept Med Genet, Chuo Ku, Chiba 2608670, Japan
[6] Miyazaki Med Coll, Dept Internal Med 3, Miyazaki 8891692, Japan
关键词
alternative splicing; cAMP; GEF; Rap1;
D O I
10.1006/geno.2001.6641
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 liver-specific protein cAMP-GEFII (also known as Epac2) belongs to a family of cyclic adenosine monophosphate (cAMP) binding proteins having guanine nucleotide exchange factor (GEF) activity (the cAMP-GEF family). Here we clone the gene EPAC2, encoding cAMP-GEFII, from a human liver cDNA library. Human EPAC2 has at least 31 exons and is mapped to human chromosome 2q31. Analyses by primer extension, reverse transcriptase-polymerase chain reaction, and in situ hybridization revealed the presence of three transcription start sites of liver-specific Epac2: two major sites! located in exon 10 and a minor site in intron 9. The same translation start site is used in all three transcripts. Liver-specific cAMP-GEFII protein, which lacks the first cAMP-binding domain and the Dishevelled/Eg1-10/Pleckstrin domain, was detected at 79 kDa by immunoblot analysis, confirming the presence of the short form of cAMP-GEFII in the liver. Liver-specific cAMP-GEFII also has GEF activity toward Rap1. These results demonstrate the presence of liver-specific cAMP-GEFII Together with the previous finding that cAMP-GEFII is responsible for cAMP-dependent exocytosis in secretory cells, our study suggests that cAMP-GEFII may have a distinct role in liver.
引用
收藏
页码:91 / 98
页数:8
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