Differential tissue-regulation of myostatin genes in the teleost fish Lates calcarifer in response to fasting. Evidence for functional differentiation

被引:40
作者
De Santis, C. [1 ]
Jerry, D. R. [1 ]
机构
[1] James Cook Univ, Sch Marine & Trop Biol, Aquaculture Genet Res Program, Townsville, Qld 4811, Australia
关键词
Myostatin; Fasting; Lates calcarifer; Tissue-expression; cis-Elements; Gene duplication; TRANSCRIPTION FACTORS; TRANSFORMING GROWTH-FACTOR-BETA-1; HOPLIAS-MALABARICUS; GENOME DUPLICATION; BETA SUPERFAMILY; FOOD-DEPRIVATION; EXPRESSION; GROWTH; RESTRICTION; LIVER;
D O I
10.1016/j.mce.2011.01.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gene or genome duplication is a fundamental evolutionary mechanism leading towards the origin of new genes, or gene functions. Myostatin (MSTN) is a negative regulator of muscle growth that in teleost fish, as a result of genome duplication, is present in double copy. This study provides evidence of differentiation of MSTN paralogs in fish by comparatively exploring their tissue-regulation in the Asian sea bass (Lotus calcarifer) when subjected to fasting stress. Results showed differential regulation as well as specific tissue-responses in the muscle, liver, gill and brain of L. calcarifer after nutritional deprivation. In particular, the LcMstn-1 expression increased in liver (similar to 4 fold) and muscle (similar to 3 fold) and diminished in brain (similar to 0.5 fold) and gill (similar to 0.5 fold) while that of LcMstn-2 remained stable in brain and muscle and was up regulated in gill (similar to 2.5 fold) and liver (similar to 2 fold). Differential regulation of Mstn paralogs was supported by in silico analyses of regulatory motifs that revealed, at least in the immediate region upstream the genes, a differentiation between Mstn-1 and Mstn-2. The Mstn-1 in particular showed a significantly higher conservation of regulatory sites among teleost species compared to its paralog indicating that this gene might have a highly conserved function in the taxon. Crown Copyright (C) 2011 Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:158 / 165
页数:8
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