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急性冷刺激激活小鼠棕色脂肪组织STAU1介导的mRNA降解途径

郭子豪 万梦瑶 聂诗琪 梁小弟

基础医学与临床2025,Vol.45Issue(10):1284-1290,7.
基础医学与临床2025,Vol.45Issue(10):1284-1290,7.DOI:10.16352/j.issn.1001-6325.2025.10.1284

急性冷刺激激活小鼠棕色脂肪组织STAU1介导的mRNA降解途径

Activation of STAU1-mediated mRNA decay pathway in brown adipose tissue of mice by acute cold stress

郭子豪 1万梦瑶 1聂诗琪 1梁小弟1

作者信息

  • 1. 新疆医科大学 基础医学院 生物化学与分子生物学教研室,新疆 乌鲁木齐 830011
  • 折叠

摘要

Abstract

Objective To investigate the effect of acute cold stimulation on the staufen1-mediated mRNA decay(SMD)pathway in brown adipose tissue of mice and the downstream regulated target genes.Methods Mice were subjected to acute cold stimulation(CS)at 4℃.After 48 hours,the brown adipose tissue of mice was extracted to detect the expression of genes including as Stau1,Ucp1 and Pparγ,and compared with mice in room temperature control group(RT).Transcriptomic sequencing was performed on the brown adipose tissue of mice in the CS group and in the RT group,and the functional enrichment analysis of differential genes was performed on the sequencing re-sults.The Stau1 gene was knocked out in the brown adipocytes of mice using CRISPR-Cas9 technology,and the ex-pression of thermogenic genes after knockout was analyzed.Results Acute cold stimulation induced the expression of Stau1 gene and promoted the degradation of downstream target genes Serpineb1,Klf2 and c-Jun in the SMD pathway(P<0.05).After Stau1 knockout,the glycolipid metabolism pathway of brown adipocytes in mice was significantly up-regulated,and the expression of thermogenesis-related genes Ucp1,Prdm16,ATP5o,Dio2 and Pgc1α was up-regulated(P<0.05).Conclusions Acute cold stimulation promotes the SMD pathway in brown adipose tissue of mice,and SMD pathway mainly regulates the metabolic and thermogenic pathways in brown adipocytes.

关键词

急性冷刺激/棕色脂肪组织/STAU1/RNA降解途径/转录组测序

Key words

acute cold stimulation/brown adipose tissue/STAU1/RNA degradation pathway/transcriptome sequencing

分类

医药卫生

引用本文复制引用

郭子豪,万梦瑶,聂诗琪,梁小弟..急性冷刺激激活小鼠棕色脂肪组织STAU1介导的mRNA降解途径[J].基础医学与临床,2025,45(10):1284-1290,7.

基金项目

国家自然科学基金(82260177) (82260177)

省部共建中亚高发病成因与防治国家重点实验室开放课题(SKL-HIDCA-2023-20) (SKL-HIDCA-2023-20)

基础医学与临床

1001-6325

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