{"title":"猪 ACSL3 基因的核心启动子识别和转录调控。","authors":"Xiaomin Li, Zijiao Guo, Xueying Ma, Huixin Liu, Wenwen Wang, Hui Tang","doi":"10.1080/10495398.2024.2430383","DOIUrl":null,"url":null,"abstract":"<p><p>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 (<i>ACSL3</i>), as a key enzyme in the process of lipid synthesis in mammals. However, no information about the core promoter of the <i>ACSL3</i> gene and its transcriptional regulation has been reported so far. In this experiment, we successfully cloned 3112 bp of the porcine <i>ACSL3</i> gene promoter region. In order to find out the core promoter of the <i>ACSL3</i> gene. The results indicated that the core promoter region of the <i>ACSL3</i> gene is located from -111 bp to -59 bp upstream of the transcription initiation site (TSS). To identify the interaction between SP1 and the <i>ACSL3</i> gene promoter, we mutated the predicted binding sites of <i>ACSL3</i> 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 <i>ACSL3</i> gene. In summary, our study identified a core promoter region of the porcine <i>ACSL3</i> gene, and the SP1 binding site is responsible for the promoter activity.</p>","PeriodicalId":7836,"journal":{"name":"Animal Biotechnology","volume":"35 1","pages":"2430383"},"PeriodicalIF":1.7000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Core promoter identification and transcriptional regulation of porcine <i>ACSL3</i> gene.\",\"authors\":\"Xiaomin Li, Zijiao Guo, Xueying Ma, Huixin Liu, Wenwen Wang, Hui Tang\",\"doi\":\"10.1080/10495398.2024.2430383\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 (<i>ACSL3</i>), as a key enzyme in the process of lipid synthesis in mammals. However, no information about the core promoter of the <i>ACSL3</i> gene and its transcriptional regulation has been reported so far. In this experiment, we successfully cloned 3112 bp of the porcine <i>ACSL3</i> gene promoter region. In order to find out the core promoter of the <i>ACSL3</i> gene. The results indicated that the core promoter region of the <i>ACSL3</i> gene is located from -111 bp to -59 bp upstream of the transcription initiation site (TSS). To identify the interaction between SP1 and the <i>ACSL3</i> gene promoter, we mutated the predicted binding sites of <i>ACSL3</i> 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 <i>ACSL3</i> gene. In summary, our study identified a core promoter region of the porcine <i>ACSL3</i> gene, and the SP1 binding site is responsible for the promoter activity.</p>\",\"PeriodicalId\":7836,\"journal\":{\"name\":\"Animal Biotechnology\",\"volume\":\"35 1\",\"pages\":\"2430383\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Animal Biotechnology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1080/10495398.2024.2430383\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/25 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Animal Biotechnology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1080/10495398.2024.2430383","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/25 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Core promoter identification and transcriptional regulation of porcine ACSL3 gene.
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 (ACSL3), as a key enzyme in the process of lipid synthesis in mammals. However, no information about the core promoter of the ACSL3 gene and its transcriptional regulation has been reported so far. In this experiment, we successfully cloned 3112 bp of the porcine ACSL3 gene promoter region. In order to find out the core promoter of the ACSL3 gene. The results indicated that the core promoter region of the ACSL3 gene is located from -111 bp to -59 bp upstream of the transcription initiation site (TSS). To identify the interaction between SP1 and the ACSL3 gene promoter, we mutated the predicted binding sites of ACSL3 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 ACSL3 gene. In summary, our study identified a core promoter region of the porcine ACSL3 gene, and the SP1 binding site is responsible for the promoter activity.
期刊介绍:
Biotechnology can be defined as any technique that uses living organisms (or parts of organisms like cells, genes, proteins) to make or modify products, to improve plants, animals or microorganisms for a specific use. Animal Biotechnology publishes research on the identification and manipulation of genes and their products, stressing applications in domesticated animals. The journal publishes full-length articles and short research communications, as well as comprehensive reviews. The journal also provides a forum for regulatory or scientific issues related to cell and molecular biology applied to animal biotechnology.
Submissions on the following topics are particularly welcome:
- Applied microbiology, immunogenetics and antibiotic resistance
- Genome engineering and animal models
- Comparative genomics
- Gene editing and CRISPRs
- Reproductive biotechnologies
- Synthetic biology and design of new genomes