Circular RNA expression in turkey skeletal muscle satellite cells is significantly altered by thermal challenge.

Meleagris gallopavo Pectoralis major circRNA differential splicing non-coding RNA

Journal

Frontiers in physiology
ISSN: 1664-042X
Titre abrégé: Front Physiol
Pays: Switzerland
ID NLM: 101549006

Informations de publication

Date de publication:
2024
Historique:
received: 05 08 2024
accepted: 28 08 2024
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 3 10 2024
Statut: epublish

Résumé

Understanding the genetic mechanisms behind muscle growth and development is crucial for improving the efficiency of animal protein production. Recent poultry studies have identified genes related to muscle development and explored how environmental stressors, such as temperature extremes, affect protein production and meat quality. Non-coding RNAs, including circular RNAs (circRNAs), play crucial roles in modulating gene expression and regulating the translation of mRNAs into proteins. This study examined circRNA expression in turkey skeletal muscle stem cells under thermal stress. The objectives were to identify and quantify circRNAs, assess circRNA abundance following RNAse R depletion, identify differentially expressed circRNAs (DECs), and predict potential microRNA (miRNA) targets for DECs and their associated genes. Cultured cells from two genetic lines (Nicholas commercial turkey and The Ohio State Random Bred Control 2) under three thermal treatments: cold (33°C), control (38°C), and hot (43°C) were compared at both the proliferation and differentiation stages. CircRNA prediction and differential expression and splicing analyses were conducted using the CIRIquant pipeline for both the untreated and RNase R depletion treated libraries. Predicted interactions between DECs and miRNAs, as well as the potential impact of circRNA secondary structure on these interactions, were investigated. A total of 11,125 circRNAs were predicted within the treatment groups, between both untreated and RNase R treated libraries. Differential expression analyses indicated that circRNA expression was significantly altered by thermal treatments and the genetic background of the stem cells. A total of 140 DECs were identified across the treatment comparisons. In general, more DECs within temperature treatment comparisons were identified in the proliferation stage and more DECs within genetic line comparisons were identified in the differentiation stage. This study highlights the significant impact of environmental stressors on non-coding RNAs and their role in gene regulation. Elucidating the role of non-coding RNAs in gene regulation can help further our understanding of muscle development and poultry production, underscoring the broader implications of this research for enhancing animal protein production efficiency.

Identifiants

pubmed: 39359572
doi: 10.3389/fphys.2024.1476487
pii: 1476487
pmc: PMC11445135
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1476487

Informations de copyright

Copyright © 2024 Powell, Velleman, Strasburg, Abrahante Lloréns and Reed.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Ashley A Powell (AA)

Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, MN, United States.

Sandra G Velleman (SG)

Department of Animal Sciences, The Ohio State University, Wooster, OH, United States.

Gale M Strasburg (GM)

Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI, United States.

Juan E Abrahante Lloréns (JE)

Minnesota Supercomputing Institute, University of Minnesota, Minneapolis, MN, United States.

Kent M Reed (KM)

Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, MN, United States.

Classifications MeSH