Key result
Knockdown of the long non-coding RNA APOA4-AS reduced APOA4 expression and decreased plasma triglyceride and total cholesterol levels in ob/ob mice.
Why the study?
Does knockdown of APOA4-AS reduce APOA4 expression and lipid levels in ob/ob mice?
Does knockdown of APOA4-AS reduce APOA4 expression and lipid levels in ob/ob mice?
Answers are grounded in this paper and cite their sources.
APOA4-AS regulates APOA4 expression via HuR, and its knockdown reduces plasma triglycerides and cholesterol in a mouse model of obesity and fatty liver disease.
Long non-coding RNAs (lncRNAs) have been shown to be critical biomarkers or therapeutic targets for human diseases. However, only a small number of lncRNAs were screened and characterized. Here, we identified 15 lncRNAs, which are associated with fatty liver disease. Among them, APOA4-AS is shown to be a concordant regulator of Apolipoprotein A-IV (APOA4) expression. APOA4-AS has a similar expression pattern with APOA4 gene. The expressions of APOA4-AS and APOA4 are both abnormally elevated in the liver of ob/ob mice and patients with fatty liver disease. Knockdown of APOA4-AS reduces APOA4 expression both in vitro and in vivo and leads to decreased levels of plasma triglyceride and total cholesterol in ob/ob mice. Mechanistically, APOA4-AS directly interacts with mRNA stabilizing protein HuR and stabilizes APOA4 mRNA. Deletion of HuR dramatically reduces both APOA4-AS and APOA4 transcripts. This study uncovers an anti-sense lncRNA (APOA4-AS), which is co-expressed with APOA4, and concordantly and specifically regulates APOA4 expression both in vitro and in vivo with the involvement of HuR.
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Qin et al. (2016) studied Fatty liver disease. Knockdown of APOA4-AS was evaluated on APOA4 expression, plasma triglyceride, and total cholesterol. Knockdown of the long non-coding RNA APOA4-AS reduced APOA4 expression and decreased plasma triglyceride and total cholesterol levels in ob/ob mice.
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