Evidence mapPaperPMID 42096909Full record

ArticlePoultry science2026

Characterization of the chicken insulin receptor gene: Genomic organization and alternative promoter regulation.

Ming Lou, Jiaxin Huang, Haoyu Luo, Fan Gao, Fang Mu, Ning Wang

Abstract read
In one paragraph

Article in Poultry science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
field-weighted citation impact
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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

6 authors.

Ming LouKey Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture and Rural Affairs, Harbin 150030, China; Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Jiaxin HuangKey Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture and Rural Affairs, Harbin 150030, China; Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Haoyu LuoKey Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture and Rural Affairs, Harbin 150030, China; Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Fan GaoKey Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture and Rural Affairs, Harbin 150030, China; Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Fang MuKey Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture and Rural Affairs, Harbin 150030, China; Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China.
Ning WangKey Laboratory of Chicken Genetics and Breeding, Ministry of Agriculture and Rural Affairs, Harbin 150030, China; Key Laboratory of Animal Genetics, Breeding and Reproduction, Education Department of Heilongjiang Province, Harbin 150030, China; College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China. Electronic address: wangning@neau.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The insulin receptor (INSR) serves as a central mediator in insulin signaling pathway, critically regulating cellular growth, metabolism, and homeostasis. While extensively characterized in mammals, the genomic architecture and transcriptional regulation of the INSR in avian species remain largely unexplored. Here, we delineated the chicken INSR gene using 5'/3' rapid amplification of cDNA ends (RACE) and RT-PCR, identifying three alternative first exons (exon 1A, 1B, and 1C) and their associated promoters. Dual-luciferase reporter assays demonstrated that each promoter exhibits distinct promoter activity and differential responsiveness to insulin and dexamethasone. Quantitative RT-PCR analysis further revealed tissue-specific expression patterns of the resulting transcript isoforms, with significant differences observed between lean and fat broiler lines. MEME motif analysis revealed that INSR promoters exhibited differential motif architecture across the species examined and among the three alternative promoters of the chicken INSR gene. Our findings establish that INSR expression in chickens is regulated by three alternative promoters-a paradigm divergent from the mammalian model. This work provides fundamental insights into the evolutionary divergence of insulin signaling in birds and establishes a transcriptional framework for investigating insulin resistance mechanisms in avian species.

Indexed as

Avian ProteinsChickensGene Expression RegulationPromoter Regions, GeneticReceptor, InsulinAnimalsInsulinAvian ProteinsInsulinReceptor, InsulinAlternative promoterGallus gallusHormonal responseInsulin receptorTranscriptional regulation

Identifiers

PMID42096909
PMCPMC13157139

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.