Evidence map›Paper›PMID 31418102›Full record

ArticleFish physiology and biochemistry2019

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 Zhang, Zhiyong Zhang, Zhenpeng Yu, Jiayi Li, Shuyin Chen, Ruijian Sun, Chaofeng Jia, Fei Zhu, Qian Meng, Shixia Xu

Abstract read
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In one paragraph

Article in Fish physiology and biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Liver Transcriptome Analysis of the Black Porgy (Life (Basel, Switzerland) · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Xinyi ZhangMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Zhiyong ZhangMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Zhenpeng YuJiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Jiayi LiJiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China.
Shuyin ChenMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China. shuyinchen89@163.com.
Ruijian SunMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Chaofeng JiaMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Fei ZhuMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Qian MengMarine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China.
Shixia XuJiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, 210023, China. xushixia78@163.com.ORCID http://orcid.org/0000-0002-0283-0986
Zhejiang Marine Fisheries Research Institute · CNNanjing Normal University · CN

Funding

Aquatic Sanxin Engineering Project of Jiangsu Province Y2016-23Independent Innovation of Agricultural Science and Technology of Jiangsu Province CX(17)2021Key Project for Jiangsu Agricultural New Variety Innovation PZCZ201744Key Research and Development (Modern Agriculture) Program of Jiangsu Province BE2016326National Natural Science Foundation of China 31570379Priority Academic Program Development of Jiangsu Higher Education Institutions PAPD
6 · The paper itself

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.

Indexed as

Cloning, MolecularEvolution, MolecularAmino Acid SequenceAnimalsGene Expression RegulationHumansInsulin-Like Growth Factor Binding ProteinsPerciformesPhylogenyTissue DistributionInsulin-Like Growth Factor Binding ProteinsAcanthopagrus schlegeliiCloningGene evolutionIGFBP-2Tissue distribution

Identifiers

PMID31418102
OpenAlexW2968648057

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.