NUCLEOTIDE-SEQUENCE AND TISSUE DISTRIBUTION OF 3 INSULIN-LIKE GROWTH FACTOR-I PROHORMONES IN SALMON

被引:92
作者
DUGUAY, SJ
PARK, LK
SAMADPOUR, M
DICKHOFF, WW
机构
[1] UNIV WASHINGTON, SCH PUBL HLTH & COMMUNITY MED, DEPT ENVIRONM HLTH, SEATTLE, WA 98195 USA
[2] NATL MARINE FISHERIES SERV, NW FISHERIES SCI CTR, SEATTLE, WA 98112 USA
关键词
D O I
10.1210/me.6.8.1202
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tissue distribution and potential alternative splicing of insulin-like growth factor I (IGF-I) messenger RNA were studied using reverse transcriptase-polymerase chain reaction (RT-PCR) on RNA from several tissues at various stages of the life cycle of coho salmon (Oncorhynchus kisutch). DNA sequence analysis of RT-PCR products revealed three IGF-I mRNA transcripts, designated Ea-1, Ea-2, and Ea-3, which code for three distinct prohormones, IGF-IA-1, IGF-IA-2, and IGF-IA-3, respectively. The E-domain of proIGF-IA-1 is 35 amino acids long and shares 77% sequence identity with the E-domain of human prolGF-IA, which is also 35 amino acids long. The proIGF-IA-2 and proIGF-IA-3 E-domains are homologous to the proIGF-IA-1 E-domain but contain 27 and 39 amino acid inserts, respectively, between Lys86 and Glu87. In the human IGF-I gene Lys86 is coded by exon 4 and Glu87 is coded by exon 6. This suggests that Ea-2 and Ea-3 transcripts may be the result of alternative splicing during pre-mRNA processing. All three transcripts were readily detectable using a solution hybridization/RNase protection assay. Furthermore, RT-PCR and DNA sequencing analysis indicate the presence of three IGF-I prohormones in another member of the Salmonidae family, the Atlantic salmon (Salmo salar). An analysis of IGF-I and -II E-domains from several vertebrates suggests that certain chemical and physical properties of the molecule are well conserved despite wide variations in primary structure. Ea-1, Ea-2, and Ea-3 transcripts were found in whole embryos, and liver, muscle, and brain of juvenile and adult salmon. At least one IGF-I transcript was found in heart, kidney, testes, ovary, adipose tissue, and spleen of juvenile salmon. These results indicate that IGF-I is expressed during embryonic development of fish, and that most tissues are capable of IGF-I mRNA production. These data also indicate that pre-mRNA transcripts can be alternatively spliced to yield at least three prohormones.
引用
收藏
页码:1202 / 1210
页数:9
相关论文
共 37 条
[1]   PARTIAL CHARACTERIZATION OF A MITOGENIC FACTOR WITH SOMATOMEDIN-LIKE ACTIVITY PRODUCED BY CULTURE WI-38 HUMAN-FIBROBLASTS [J].
ATKISON, PR ;
BALA, RM .
JOURNAL OF CELLULAR PHYSIOLOGY, 1981, 107 (03) :317-327
[2]   RELEASE OF SOMATOMEDIN-LIKE ACTIVITY BY CULTURED WI-38 HUMAN-FIBROBLASTS [J].
ATKISON, PR ;
WEIDMAN, ER ;
BHAUMICK, B ;
BALA, RM .
ENDOCRINOLOGY, 1980, 106 (06) :2006-2012
[3]  
AUSUBEL FM, 1990, CURRENT PROTOCOLS MO
[4]   IMPAIRED FORMATION OF THE TERNARY INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN COMPLEX IN PATIENTS WITH HYPOGLYCEMIA DUE TO NONISLET CELL TUMORS [J].
BAXTER, RC ;
DAUGHADAY, WH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (04) :696-702
[5]   SEQUENCE OF A CDNA CLONE ENCODING HUMAN PREPROINSULIN-LIKE GROWTH FACTOR-II [J].
BELL, GI ;
MERRYWEATHER, JP ;
SANCHEZPESCADOR, R ;
STEMPIEN, MM ;
PRIESTLEY, L ;
SCOTT, J ;
RALL, LB .
NATURE, 1984, 310 (5980) :775-777
[6]   ISOLATION OF THE HUMAN INSULIN-LIKE GROWTH-FACTOR GENES - INSULIN-LIKE GROWTH FACTOR-II AND INSULIN GENES ARE CONTIGUOUS [J].
BELL, GI ;
GERHARD, DS ;
FONG, NM ;
SANCHEZPESCADOR, R ;
RALL, LB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (19) :6450-6454
[7]   MOLECULAR MECHANISMS OF PROTEIN SECRETION - THE ROLE OF THE SIGNAL SEQUENCE [J].
BRIGGS, MS ;
GIERASCH, LM .
ADVANCES IN PROTEIN CHEMISTRY, 1986, 38 :109-180
[8]   NUCLEOTIDE-SEQUENCE AND GROWTH HORMONE-REGULATED EXPRESSION OF SALMON INSULIN-LIKE GROWTH FACTOR-I MESSENGER-RNA [J].
CAO, QP ;
DUGUAY, SJ ;
PLISETSKAYA, E ;
STEINER, DF ;
CHAN, SJ .
MOLECULAR ENDOCRINOLOGY, 1989, 3 (12) :2005-2010
[9]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[10]  
Chou P Y, 1978, Adv Enzymol Relat Areas Mol Biol, V47, P45