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Molecular cloning and expression pattern of IGFBP-2a in black porgy (Acanthopagrus schlegelii) and evolutionary analysis of IGFBP-2s in the species of Perciformes.
Zhang, Xinyi; Zhang, Zhiyong; Yu, Zhenpeng; Li, Jiayi; Chen, Shuyin; Sun, Ruijian; Jia, Chaofeng; Zhu, Fei; Meng, Qian; Xu, Shixia.
Afiliación
  • Zhang X; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
  • Zhang Z; Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Yu Z; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
  • Li J; Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Chen S; Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
  • Sun R; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China. shuyinchen89@163.com.
  • Jia C; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
  • Zhu F; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
  • Meng Q; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
  • Xu S; Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Fish Physiol Biochem ; 45(5): 1731-1745, 2019 Oct.
Article en En | MEDLINE | ID: mdl-31418102
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Perciformes / Regulación de la Expresión Génica / Clonación Molecular / Proteínas de Unión a Factor de Crecimiento Similar a la Insulina / Evolución Molecular Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Fish Physiol Biochem Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Perciformes / Regulación de la Expresión Génica / Clonación Molecular / Proteínas de Unión a Factor de Crecimiento Similar a la Insulina / Evolución Molecular Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Fish Physiol Biochem Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: Países Bajos