Saved in:
Bibliographic Details
Main Authors: Ullah, Kalim, Hossain, Aslam, Cao, Mingyue, Xue, Liangyi, Wang, Yajun
Format: Artículo científico
Language:en
Published: Scientific reports 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/39905090/
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1868266247440826368
author Ullah, Kalim
Hossain, Aslam
Cao, Mingyue
Xue, Liangyi
Wang, Yajun
author_facet Ullah, Kalim
Hossain, Aslam
Cao, Mingyue
Xue, Liangyi
Wang, Yajun
Ullah, Kalim
Hossain, Aslam
Cao, Mingyue
Xue, Liangyi
Wang, Yajun
collection PubMed - marine biology
contents Target miRNA identification for the LPL gene in large yellow croaker (Larimichthys crocea). Ullah, Kalim Hossain, Aslam Cao, Mingyue Xue, Liangyi Wang, Yajun Animals Perciformes MicroRNAs Lipoprotein Lipase 3' Untranslated Regions Computational Biology Lipid Metabolism Gene Expression Regulation Liver Fish Proteins MicroRNA (miRNA), a conservatively evolved single-stranded non-coding RNA, exerts pivotal control over the appearance of target genes and several biological processes. This study conducted a comprehensive screening of candidate microRNAs (miRNAs) associated with Lipoprotein Lipase (LPL) in the large yellow croaker (Larimichthys crocea), utilizing sophisticated bioinformatics techniques across the species' muscular and hepatic tissues. The bioinformatics analysis facilitated the compilation and examination of miRNA datasets specific to these tissues. The investigation culminated in the identification of miR-84a and miR-1231-5p as key miRNAs that modulate fat hydrolysis, highlighting their potential roles in lipid metabolism. Subsequent in-depth analysis further implicated these miRNAs, along with miR-891a, as prospective targets of LPL, suggesting their integral involvement in the regulation of this critical enzyme. Validation of these bioinformatics predictions was conducted through the construction of double luciferase reporters concealing the LPL 3' untranslated region (3'UTR), substantiating that miR-84a and miR-1231-5p can modulate LPL expression via the LPL 3'UTR. Conversely, miR-891a was not concerned with this regulatory mechanism. Site-directed mutagenesis experiments elucidated the specificity of the interaction sequences. Quantitative PCR assays suggested that miR-84a and miR-1231-5p might influence LPL expression during the starvation phase, intimating the regulatory role of miRNA in fatty acid metabolism within hepatic and muscular tissue under starvation. These findings offer a nuanced understanding of LPL's molecular functionality under stress conditions in fish, emphasizing the regulatory dynamics of miRNA during metabolic stress.
format Artículo científico
id pubmed_39905090
institution PubMed
language en
publishDate 2025
publisher Scientific reports
record_format pubmed
spellingShingle Target miRNA identification for the LPL gene in large yellow croaker (Larimichthys crocea).
Ullah, Kalim
Hossain, Aslam
Cao, Mingyue
Xue, Liangyi
Wang, Yajun
Animals
Perciformes
MicroRNAs
Lipoprotein Lipase
3' Untranslated Regions
Computational Biology
Lipid Metabolism
Gene Expression Regulation
Liver
Fish Proteins
Target miRNA identification for the LPL gene in large yellow croaker (Larimichthys crocea). Ullah, Kalim Hossain, Aslam Cao, Mingyue Xue, Liangyi Wang, Yajun Animals Perciformes MicroRNAs Lipoprotein Lipase 3' Untranslated Regions Computational Biology Lipid Metabolism Gene Expression Regulation Liver Fish Proteins MicroRNA (miRNA), a conservatively evolved single-stranded non-coding RNA, exerts pivotal control over the appearance of target genes and several biological processes. This study conducted a comprehensive screening of candidate microRNAs (miRNAs) associated with Lipoprotein Lipase (LPL) in the large yellow croaker (Larimichthys crocea), utilizing sophisticated bioinformatics techniques across the species' muscular and hepatic tissues. The bioinformatics analysis facilitated the compilation and examination of miRNA datasets specific to these tissues. The investigation culminated in the identification of miR-84a and miR-1231-5p as key miRNAs that modulate fat hydrolysis, highlighting their potential roles in lipid metabolism. Subsequent in-depth analysis further implicated these miRNAs, along with miR-891a, as prospective targets of LPL, suggesting their integral involvement in the regulation of this critical enzyme. Validation of these bioinformatics predictions was conducted through the construction of double luciferase reporters concealing the LPL 3' untranslated region (3'UTR), substantiating that miR-84a and miR-1231-5p can modulate LPL expression via the LPL 3'UTR. Conversely, miR-891a was not concerned with this regulatory mechanism. Site-directed mutagenesis experiments elucidated the specificity of the interaction sequences. Quantitative PCR assays suggested that miR-84a and miR-1231-5p might influence LPL expression during the starvation phase, intimating the regulatory role of miRNA in fatty acid metabolism within hepatic and muscular tissue under starvation. These findings offer a nuanced understanding of LPL's molecular functionality under stress conditions in fish, emphasizing the regulatory dynamics of miRNA during metabolic stress.
title Target miRNA identification for the LPL gene in large yellow croaker (Larimichthys crocea).
topic Animals
Perciformes
MicroRNAs
Lipoprotein Lipase
3' Untranslated Regions
Computational Biology
Lipid Metabolism
Gene Expression Regulation
Liver
Fish Proteins
url https://pubmed.ncbi.nlm.nih.gov/39905090/