| 注册
首页|期刊导航|农业生物技术学报|奶山羊ACSL6基因启动子克隆与转录活性分析

奶山羊ACSL6基因启动子克隆与转录活性分析

熊畑畑 吴钰 邵钺馨 陈冲 王琬婷 程菲 李聪

农业生物技术学报2025,Vol.33Issue(1):124-133,10.
农业生物技术学报2025,Vol.33Issue(1):124-133,10.DOI:10.3969/j.issn.1674-7968.2025.01.011

奶山羊ACSL6基因启动子克隆与转录活性分析

Cloning and Transcriptional Activity Analysis of ACSL6 Gene Promoter in Dairy Goats(Capra hircus)

熊畑畑 1吴钰 1邵钺馨 1陈冲 1王琬婷 1程菲 1李聪1

作者信息

  • 1. 西北农林科技大学动物科技学院/陕西省动物遗传育种与繁殖重点实验室,杨凌 712100
  • 折叠

摘要

Abstract

Acyl-CoA synthetase long chain family member 6(ACSL6),a key enzyme in the uptake and transport of free fatty acids,is involved in the regulation of fatty acid metabolism during lactation in dairy animals.This study aimed to preliminarily investigate the transcriptional regulation mechanism of A CSL6 gene(Gene ID:XM_018050725.1)through promoter cloning,bioinformatics analysis and diluciferase activity detection in dairy goats(Capra hirc us).The full-length sequence of the ACSL6 promoter was obtained by PCR amplification using the blood genomic DNA of Xinong Saanen dairy goats as a template.The sequence features of the binding sites and promoter regions with high prediction scores were screened using bioinformatics analysis software.The promoter deletion fragment vectors were cloned and constructed,which were co-transfected with the internal reference vectors into the mammary epithelial cells of dairy goats,and the promoter active regions were identified by dual luciferase activity assay.The results showed that the full-length sequence of the ACSL6 promoter was 2 108 bp.The multiple transcription factor binding sites were existed in the ACSL6 promoter.The two CpG islands with lengths of 101 and 460 bp were identified in the promoter sequences of-907~-807 bp and-513~-54 bp,respectively.The nine deletions obtained from the cloning were analysed by dual-luciferase activity,and it was found that the core region of the ACSL6 promoter was located at-170~-33 bp,and there might be negative regulatory elements upstream of the transcriptional start site at-2 004~-1 707 bp,-1 334~-957 bp,and-584~-271 bp.This study provides basic information to reveal the molecular mechanism of ACSL6 regulating milk fat metabolism in dairy goats,and provides a reference to improve the quality of goat milk at the molecular level.

关键词

酰基辅酶A合成酶长链家族成员6(ACSL6)/启动子克隆/片段缺失分析/生物信息学分析/转录因子

Key words

Acyl-CoA synthetase long chain family member 6(ACSL6)/Promoter cloning/Fragment deletion analysis/Bioinformatics analysis/Transcription factor

分类

农业科技

引用本文复制引用

熊畑畑,吴钰,邵钺馨,陈冲,王琬婷,程菲,李聪..奶山羊ACSL6基因启动子克隆与转录活性分析[J].农业生物技术学报,2025,33(1):124-133,10.

基金项目

国家重点研发计划(2022YFD1300203) (2022YFD1300203)

陕西省畜禽育种"两链"融合重点专项(2022GD-TSLD-46-0203) (2022GD-TSLD-46-0203)

农业生物技术学报

OA北大核心

1674-7968

访问量3
|
下载量0
段落导航相关论文