Literature DB >> 8185811

Differential expression and hormonal regulation of alternatively spliced IGF-I mRNA transcripts in salmon.

S J Duguay1, P Swanson, W W Dickhoff.   

Abstract

Salmon have been shown to express alternatively spliced IGF-I mRNA transcripts coding for four different IGF-I prohormones. These transcripts, now designated Ea-1, Ea-2, Ea-3 and Ea-4, differ in size due to the inclusion of additional sequences in the E domain-coding region of the molecule. In this study, the tissue distribution and hormonal regulation of expression of alternatively spliced IGF-I mRNA transcripts were investigated in coho salmon. IGF-I mRNAs were detected by solution hybridization/RNase protection assay in all tissues examined. GH treatment significantly increased hepatic IGF-I mRNA content. Hepatic IGF-I mRNA levels were not influenced by prolactin or somatolactin. Heart, fat, brain, kidney, spleen and ovary IGF-I mRNA levels were not affected by GH, prolactin or somatolactin. Ea-1, Ea-3 and Ea-4 mRNA transcripts were detectable in the liver, and Ea-1 and Ea-3 levels increased dramatically in response to GH treatment, whereas the amount of Ea-4 mRNA was unchanged. Most non-hepatic tissues expressed only the Ea-4 transcript, and expression was not influenced by GH, prolactin or somatolactin. Ea-1 and Ea-3 transcripts were visible in gill samples from fish treated with GH. The ovaries of juvenile fish expressed Ea-1, Ea-2 and Ea-4. The amounts of these transcripts were not changed by gonadotrophin treatment. During smoltification of juvenile coho salmon, liver and gill IGF-I mRNA levels increased with increasing plasma GH and thyroxine concentrations. Muscle, brain and ovary IGF-I mRNA levels were unchanged during this period. These data suggest that the liver is a major site of IGF-I production in response to GH. Heart, fat, brain, kidney, spleen and ovary did not show increased IGF-I mRNA levels in response to GH treatment. GH and prolactin had inconsistent effects on muscle IGF-I mRNA levels. Somatolactin and a gonadotrophin preparation did not stimulate IGF-I expression in tissues of juvenile fish. Differences in tissue GH responsiveness can be partially explained by the expression of alternatively spliced IGF-I mRNAs. Of the four hepatic IGF-I mRNA transcripts, Ea-1 and Ea-3 are GH-responsive, while Ea-2 and Ea-4 are not. Most non-hepatic tissues express only the Ea-4 transcript, and IGF-I mRNA levels do not increase after GH treatment. The increased IGF-I mRNA levels observed in gill tissue during smoltification suggest that other factors, in addition to GH, may regulate IGF-I expression.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 8185811     DOI: 10.1677/jme.0.0120025

Source DB:  PubMed          Journal:  J Mol Endocrinol        ISSN: 0952-5041            Impact factor:   5.098


  11 in total

1.  Distinct organ-specific up- and down-regulation of IGF-I and IGF-II mRNA in various organs of a GH-overexpressing transgenic Nile tilapia.

Authors:  Elisabeth Eppler; Giorgi Berishvili; Peter Mazel; Antje Caelers; Gyulin Hwang; Norman Maclean; Manfred Reinecke
Journal:  Transgenic Res       Date:  2009-08-11       Impact factor: 2.788

Review 2.  The complexity of the IGF1 gene splicing, posttranslational modification and bioactivity.

Authors:  Anastassios Philippou; Maria Maridaki; Spiros Pneumaticos; Michael Koutsilieris
Journal:  Mol Med       Date:  2014-05-07       Impact factor: 6.354

3.  Insulin-like growth factors I and II in starry flounder (Platichthys stellatus): molecular cloning and differential expression during embryonic development.

Authors:  Yongjiang Xu; Kun Zang; Xuezhou Liu; Bao Shi; Cunyu Li; Xueying Shi
Journal:  Fish Physiol Biochem       Date:  2014-11-26       Impact factor: 2.794

4.  Growth hormone and two forms of insulin-like growth factors I in the giant grouper (Epinephelus lanceolatus): molecular cloning and characterization of tissue distribution.

Authors:  Haiyan Dong; Lingxian Zeng; Da Duan; Haifa Zhang; Yunxin Wang; Wensheng Li; Haoran Lin
Journal:  Fish Physiol Biochem       Date:  2008-05-30       Impact factor: 2.794

5.  Evidences for involvement of growth hormone and insulin-like growth factor in ovarian development of starry flounder (Platichthys stellatus).

Authors:  Yongjiang Xu; Bin Wang; Xuezhou Liu; Bao Shi; Kun Zang
Journal:  Fish Physiol Biochem       Date:  2016-11-02       Impact factor: 2.794

6.  Seasonal and sex-specific mRNA levels of key endocrine genes in adult yellow perch (Perca flavescens) from Lake Erie.

Authors:  S G Lynn; K A Powell; D F Westneat; B S Shepherd
Journal:  Mar Biotechnol (NY)       Date:  2008-09-23       Impact factor: 3.619

7.  Cloning of Russian sturgeon (Acipenser gueldenstaedtii) growth hormone and insulin-like growth factor I and their expression in male and female fish during the first period of growth.

Authors:  S Yom Din; A Hurvitz; D Goldberg; K Jackson; B Levavi-Sivan; G Degani
Journal:  J Endocrinol Invest       Date:  2008-03       Impact factor: 4.256

8.  Differential gene expression during smoltification of Atlantic salmon (Salmo salar L.): a first large-scale microarray study.

Authors:  Paul J Seear; Stephen N Carmichael; Richard Talbot; John B Taggart; James E Bron; Glen E Sweeney
Journal:  Mar Biotechnol (NY)       Date:  2009-07-08       Impact factor: 3.619

Review 9.  Endocrine and Local IGF-I in the Bony Fish Immune System.

Authors:  Anne-Constance Franz; Oliver Faass; Bernd Köllner; Natallia Shved; Karl Link; Ayako Casanova; Michael Wenger; Helena D'Cotta; Jean-François Baroiller; Oliver Ullrich; Manfred Reinecke; Elisabeth Eppler
Journal:  Biology (Basel)       Date:  2016-01-26

10.  Lysine and Leucine Deficiencies Affect Myocytes Development and IGF Signaling in Gilthead Sea Bream (Sparus aurata).

Authors:  Sheida Azizi; Mohammad Ali Nematollahi; Bagher Mojazi Amiri; Emilio J Vélez; Esmail Lutfi; Isabel Navarro; Encarnación Capilla; Joaquim Gutiérrez
Journal:  PLoS One       Date:  2016-01-25       Impact factor: 3.240

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