Identification of a novel leptin receptor duplicate in Atlantic salmon: Expression analyses in different life stages and in response to feeding status.

Autor: Angotzi AR; Department of Biology, University of Bergen, Thormølensgate 55, Bergen 5020, Norway., Stefansson SO; Department of Biology, University of Bergen, Thormølensgate 55, Bergen 5020, Norway., Nilsen TO; Uni Research Environment, Thormøhlensgate 49 B, N-5006 Bergen, Norway., Øvrebø JI; Department of Biology, University of Bergen, Thormølensgate 55, Bergen 5020, Norway; Huntsman Cancer Institute, University of Utah, 2000 Circle of Hope Drive, Salt Lake City, UT 84112, USA., Andersson E; Institute of Marine Research, P.O. Box 187, Nordnes, N-5817 Bergen, Norway., Taranger GL; Institute of Marine Research, P.O. Box 187, Nordnes, N-5817 Bergen, Norway., Rønnestad I; Department of Biology, University of Bergen, Thormølensgate 55, Bergen 5020, Norway. Electronic address: ivar.ronnestad@uib.no.
Jazyk: angličtina
Zdroj: General and comparative endocrinology [Gen Comp Endocrinol] 2016 Sep 01; Vol. 235, pp. 108-119. Date of Electronic Publication: 2016 Jun 08.
DOI: 10.1016/j.ygcen.2016.06.004
Abstrakt: In recent years rapidly growing research has led to identification of several fish leptin orthologs and numerous duplicated paralogs possibly arisen from the third and fourth round whole genome duplication (3R and 4R WGD) events. In this study we identify in Atlantic salmon a duplicated LepRA gene, named LepRA2, that further extend possible evolutionary scenarios of the leptin and leptin receptor system. The 1121 amino acid sequence of the novel LepRA2 shares 80% sequence identity with the LepRA1 paralog, and contains the protein motifs typical of the functional (long form) leptin receptor in vertebrates. In silico predictions showed similar electrostatic properties of LepRA1 and LepRA2 and high sequence conservation at the leptin interaction surfaces within the CHR/leptin-binding and FNIII domains, suggesting conserved functional specificity between the two duplicates. Analysis of temporal expression profiles during pre-hatching stages indicate that both transcripts are involved in modulating leptin developmental functions, although the LepRA1 paralog may play a major role as the embryo complexity increases. There is ubiquitous distribution of LepRs underlying pleiotropism of leptin in all tissues investigated. LepRA1 and LepRA2 are differentially expressed with LepRA1 more abundant than LepRA2 in most of the tissues investigated, with the only exception of liver. Analysis of constitutive LepRA1 and LepRA2 expression in brain and liver at parr, post-smolt and adult stages reveal striking spatial divergence between the duplicates at all stages investigated. This suggests that, beside increased metabolic requirements, leptin sensitivity in the salmon brain might be linked to important variables such as habitat, ecology and life cycle. Furthermore, leptins and LepRs mRNAs in the brain showed gene-specific variability in response to long term fasting, suggesting that leptin's roles as modulator of nutritional status in Atlantic salmon might be governed by distinct genetic evolutionary processes and distinct functions between the paralogs.
(Copyright © 2016 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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