Literature DB >> 31418102

Molecular cloning and expression pattern of IGFBP-2a in black porgy (Acanthopagrus schlegelii) and evolutionary analysis of IGFBP-2s in the species of Perciformes.

Xinyi Zhang1,2, Zhiyong Zhang1, Zhenpeng Yu2, Jiayi Li2, Shuyin Chen3, Ruijian Sun1, Chaofeng Jia1, Fei Zhu1, Qian Meng1, Shixia Xu4.   

Abstract

Insulin-like growth factor-binding protein-2 (IGFBP-2) plays a key role in regulating growth and development by its affinity with insulin-like growth factors (IGFs). In this study, we cloned the coding sequence (CDS) of IGFBP-2a from the black porgy (Acanthopagrus schlegelii) muscle and identified that the full-length CDS of IGFBP-2a was 882 bp. Real-time quantitative PCR revealed that IGFBP-2a was most abundant in the liver of the black porgy and backcross breed (F1♀×black porgy♂) but remained lower in each tested tissue in self-cross breed (F1♀×F1♂). In addition, the IGFBP-2a expression in the liver of three breeds showed a negative correlation with their growth rates, indicating that the IGFBP-2a played a growth-inhibiting role in the three breeds. We further identified 810 bp IGFBP-2b gene from the draft genome of black porgy. Finally, we examined the IGFBP-2a and IGFBP-2b genes by scanning the genomes of the species of Perciformes and found the IGFBP-2 gene duplication took place earlier than the divergence of perciform species. Interestingly, six positively selected sites were detected in both Perciformes IGFBP-2 genes, although both genes were identified to be under purifying selection. Specially, these positively selected sites were located in the functional domains, suggesting these sites played key roles in the growth of Perciformes. Our study partially explains the molecular basis for the prepotency in black porgy hybrids, which will provide guidance for their cultivation in the future.

Entities:  

Keywords:  Acanthopagrus schlegelii; Cloning; Gene evolution; IGFBP-2; Tissue distribution

Mesh:

Substances:

Year:  2019        PMID: 31418102     DOI: 10.1007/s10695-019-00665-y

Source DB:  PubMed          Journal:  Fish Physiol Biochem        ISSN: 0920-1742            Impact factor:   2.794


  64 in total

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Authors:  Diego Safian; Eduardo N Fuentes; Juan Antonio Valdés; Alfredo Molina
Journal:  J Endocrinol       Date:  2012-04-12       Impact factor: 4.286

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Authors:  Leon A Bach; Stephen J Headey; Raymond S Norton
Journal:  Trends Endocrinol Metab       Date:  2005-07       Impact factor: 12.015

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Journal:  Genetics       Date:  1998-03       Impact factor: 4.562

7.  Divergent regulation of insulin-like growth factor binding protein genes in cultured Atlantic salmon myotubes under different models of catabolism and anabolism.

Authors:  Daniel Garcia de la Serrana; Eduardo N Fuentes; Samuel A M Martin; Ian A Johnston; Daniel J Macqueen
Journal:  Gen Comp Endocrinol       Date:  2017-01-19       Impact factor: 2.822

8.  Identification of the amniotic fluid insulin-like growth factor binding protein-1 phosphorylation sites and propensity to proteolysis of the isoforms.

Authors:  Lorenzo Dolcini; Alberto Sala; Monica Campagnoli; Sara Labò; Maurizia Valli; Livia Visai; Lorenzo Minchiotti; Hugo L Monaco; Monica Galliano
Journal:  FEBS J       Date:  2009-09-17       Impact factor: 5.542

9.  FasParser: a package for manipulating sequence data.

Authors:  Yan-Bo Sun
Journal:  Zool Res       Date:  2017-03-18

10.  Duplication of the IGFBP-2 gene in teleost fish: protein structure and functionality conservation and gene expression divergence.

Authors:  Jianfeng Zhou; Wenhong Li; Hiroyasu Kamei; Cunming Duan
Journal:  PLoS One       Date:  2008-12-12       Impact factor: 3.240

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  1 in total

1.  Sex-Specific Control of Muscle Mass: Elevated IGFBP Proteolysis and Reductions of IGF-1 Levels Are Associated with Substantial Loss of Carcass Weight in Male DU6PxIGFBP-2 Transgenic Mice.

Authors:  Daniela Ohde; Michael Walz; Christina Walz; Antonia Noce; Julia Brenmoehl; Martina Langhammer; Andreas Hoeflich
Journal:  Cells       Date:  2020-09-26       Impact factor: 6.600

  1 in total

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