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ArticleMolecular biology reports2024

Expression mechanisms of mir-486-5p and its host gene sANK1 in porcine muscle.

Xiaoping Guo, Ganqiu Lan, Qinyang Jiang, Yafen Guo, Yiqiang Ouyang, Jing Liang, Mingyuan Zhang

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Xiaoping GuoLaboratory Animal Center, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Ganqiu LanCollege of Animal Science and Technology, Guangxi University, Nanning, 530004, Guangxi, China.
Qinyang JiangCollege of Animal Science and Technology, Guangxi University, Nanning, 530004, Guangxi, China.
Yafen GuoCollege of Animal Science and Technology, Guangxi University, Nanning, 530004, Guangxi, China.
Yiqiang OuyangLaboratory Animal Center, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Jing LiangCollege of Animal Science and Technology, Guangxi University, Nanning, 530004, Guangxi, China. liangjing@gxu.edu.cn.
Mingyuan ZhangLaboratory Animal Center, Guangxi Medical University, Nanning, 530021, Guangxi, China. Bio_MYZhang@sr.gxmu.edu.cn.

Funding

National Modern Agricultural Industrial Technological System in Guangxi pig industry innova-tion team project nycytxgxcxtd-03-15National Natural Science Foundation of China 30960058
6 · The paper itself

Abstract

backgroundMiR-486-5p has been identified as a crucial regulator of the PI3K/AKT signalling pathway, which plays a significant role in skeletal muscle development. Its host gene, sANK1, is also essential for skeletal muscle development. However, the understanding of porcine miR-486-5p and sANK1 has been limited. METHODS AND

resultsIn this study, PCR analyses revealed a positive correlation between the expression of miR-486-5p and sANK1 in the longissimus dorsi muscle of the Bama mini-pig and Landrace-pig, as well as during myoblast differentiation. Furthermore, the expression of miR-486-5p/sANK1 was higher in the Bama mini-pig compared to the Landrace-pig. There was a total of 18 single nucleotide polymorphisms (SNP) present in the sANK1 promoter region. Among these SNPs, 14 of them resulted in alterations in transcription factor binding sites (TFBs). Additionally, the promoter fluorescence assay demonstrated that the activity of the sANK1 promoter derived from the Bama mini-pig was significantly higher compared to Landrace-pig. It is worth noting that ten regulatory SNPs have the potential to influence the activity of the sANK1 promoter. A nuclear mutation A-G located at position - 401 (relative to the transcription start site) in the Bama mini-pig was identified, which creates a putative TFB motif for MyoD.

conclusionsThe findings presented in this study offer fundamental molecular knowledge and expression patterns of miR-486-5p/sANK1, which can be valuable for gaining a deeper understanding of the gene's involvement in porcine skeletal muscle development, and meat quality.

Indexed as

MicroRNAsMuscle, SkeletalPolymorphism, Single NucleotidePromoter Regions, GeneticAnimalsBinding SitesCell DifferentiationGene Expression RegulationMuscle DevelopmentMyoblastsMyoD ProteinSignal TransductionSwineMicroRNAsMyoD ProteinmiR-486-5pPigsANK1Skeletal muscle

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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.