{"title":"Anoxia-responsive microRNA profile of freshwater turtle red skeletal muscle","authors":"Tighe Bloskie, Kenneth B. Storey","doi":"10.1016/j.genrep.2025.102302","DOIUrl":null,"url":null,"abstract":"<div><div>The red-eared slider (<em>Trachemys scripta elegans</em>) is a uniquely impressive vertebrate facultative anaerobe, capable of 18 weeks without oxygen at 3 °C. Metabolic rate depression (∼85 %) is the core feature of anaerobiosis and is characterized by the suppression of costly processes like protein synthesis/decay and the cell cycle. The elucidation of microRNA (miRNA) action in support of animal extreme stress adaptation is increasing, but is currently lacking in <em>T.s. elegans</em> anoxia tolerance. Here, we use small RNA sequencing and subsequent bioinformatic analyses to identify differentially expressed miRNA and predicted target pathways in 20 h anoxic red skeletal muscle of red-eared slider turtles. Of the 52 mapped miRNA species, we identify two that were upregulated (miR-2114-5p, let-7f-5p) and two that were downregulated (miR-1260b, miR-5100) under 20 h anoxic conditions (|FC| > 1.5; <em>p</em> < 0.05). KEGG and GO analysis predict miRNA contribute to the aerobic to anaerobic respiration shift and outline miRNA-mediated inhibition of numerous gene sets in (1) protein turnover, (2) RNA turnover and (3) the cell cycle. Conversely, alleviated miRNA interference in branched amino acid biosynthesis, arachidonic acid and linolenic acid metabolism suggest a role in atrophy resistance of skeletal muscles.</div></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"40 ","pages":"Article 102302"},"PeriodicalIF":0.9000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S245201442500175X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
The red-eared slider (Trachemys scripta elegans) is a uniquely impressive vertebrate facultative anaerobe, capable of 18 weeks without oxygen at 3 °C. Metabolic rate depression (∼85 %) is the core feature of anaerobiosis and is characterized by the suppression of costly processes like protein synthesis/decay and the cell cycle. The elucidation of microRNA (miRNA) action in support of animal extreme stress adaptation is increasing, but is currently lacking in T.s. elegans anoxia tolerance. Here, we use small RNA sequencing and subsequent bioinformatic analyses to identify differentially expressed miRNA and predicted target pathways in 20 h anoxic red skeletal muscle of red-eared slider turtles. Of the 52 mapped miRNA species, we identify two that were upregulated (miR-2114-5p, let-7f-5p) and two that were downregulated (miR-1260b, miR-5100) under 20 h anoxic conditions (|FC| > 1.5; p < 0.05). KEGG and GO analysis predict miRNA contribute to the aerobic to anaerobic respiration shift and outline miRNA-mediated inhibition of numerous gene sets in (1) protein turnover, (2) RNA turnover and (3) the cell cycle. Conversely, alleviated miRNA interference in branched amino acid biosynthesis, arachidonic acid and linolenic acid metabolism suggest a role in atrophy resistance of skeletal muscles.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.