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mir-486-5p 及其宿主基因 sANK1 在猪肌肉中的表达机制。

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

机构信息

Laboratory Animal Center, Guangxi Medical University, Nanning, 530021, Guangxi, China.

College of Animal Science and Technology, Guangxi University, Nanning, 530004, Guangxi, China.

出版信息

Mol Biol Rep. 2024 Jul 23;51(1):840. doi: 10.1007/s11033-024-09773-2.

Abstract

BACKGROUND

MiR-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 RESULTS

In 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.

CONCLUSIONS

The 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.

摘要

背景

miR-486-5p 已被鉴定为 PI3K/AKT 信号通路的关键调节因子,该通路在骨骼肌发育中起着重要作用。其宿主基因 sANK1 对于骨骼肌发育也是必不可少的。然而,人们对猪 miR-486-5p 和 sANK1 的了解有限。

方法和结果

在这项研究中,PCR 分析显示 miR-486-5p 和 sANK1 在巴马小型猪和长白猪背最长肌中的表达呈正相关,并且在肌母细胞分化过程中也是如此。此外,miR-486-5p/sANK1 的表达在巴马小型猪中高于长白猪。sANK1 启动子区域共存在 18 个单核苷酸多态性(SNP)。其中 14 个 SNP 导致转录因子结合位点(TFB)发生改变。此外,启动子荧光测定表明,来自巴马小型猪的 sANK1 启动子的活性明显高于长白猪。值得注意的是,有 10 个调节性 SNP 有可能影响 sANK1 启动子的活性。在巴马小型猪中,在位置 -401(相对于转录起始位点)处发现了一个核突变 A-G,该突变创造了一个用于 MyoD 的假定 TFB 基序。

结论

本研究提供了 miR-486-5p/sANK1 的基本分子知识和表达模式,这对于深入了解该基因在猪骨骼肌发育和肉质中的作用具有重要意义。

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