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猪基因的核心启动子鉴定和转录调控。

Core promoter identification and transcriptional regulation of porcine gene.

机构信息

Key Laboratory of Efficient Utilization of Non-grain Feed Resources (Co-construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Shandong Agricultural University, Taian, Shandong Province, China.

Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Taian, Shandong Province, China.

出版信息

Anim Biotechnol. 2024 Nov;35(1):2430383. doi: 10.1080/10495398.2024.2430383. Epub 2024 Nov 25.

Abstract

Intramuscular fat (IMF) content is an important factor that affects the edible and processing quality of pork. Studying the transcriptional regulation mechanisms of genes affecting intramuscular fat deposition can provide theoretical support for genetic improvement in pigs. Long-chain fatty acyl-CoA synthase 3 (), as a key enzyme in the process of lipid synthesis in mammals. However, no information about the core promoter of the gene and its transcriptional regulation has been reported so far. In this experiment, we successfully cloned 3112 bp of the porcine gene promoter region. In order to find out the core promoter of the gene. The results indicated that the core promoter region of the gene is located from -111 bp to -59 bp upstream of the transcription initiation site (TSS). To identify the interaction between SP1 and the gene promoter, we mutated the predicted binding sites of gene promoter. The results showed that the activity of the promoter was decreased by site-specific mutagenesis of the SP1 transcription factor binding site, while overexpression of SP1 increased the expression of the gene. In summary, our study identified a core promoter region of the porcine gene, and the SP1 binding site is responsible for the promoter activity.

摘要

肌内脂肪(IMF)含量是影响猪肉食用和加工品质的重要因素。研究影响肌内脂肪沉积的基因的转录调控机制可为猪的遗传改良提供理论支持。长链脂肪酸酰基辅酶 A 合酶 3()是哺乳动物脂质合成过程中的关键酶。然而,目前尚未报道关于基因核心启动子及其转录调控的信息。在本实验中,我们成功克隆了猪基因启动子区域的 3112bp。为了找出基因的核心启动子。结果表明,基因的核心启动子区域位于转录起始位点(TSS)上游的-111bp 至-59bp。为了鉴定 SP1 与基因启动子之间的相互作用,我们突变了基因启动子的预测结合位点。结果表明,SP1 转录因子结合位点的特异性突变降低了启动子的活性,而过表达 SP1 则增加了基因的表达。总之,我们的研究鉴定了猪基因的核心启动子区域,并且 SP1 结合位点负责启动子活性。

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