» Articles » PMID: 24966054

Thermal Plasticity of the MiRNA Transcriptome During Senegalese Sole Development

Overview
Journal BMC Genomics
Publisher Biomed Central
Specialty Genetics
Date 2014 Jun 27
PMID 24966054
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Several miRNAs are known to control myogenesis in vertebrates. Some of them are specifically expressed in muscle while others have a broader tissue expression but are still involved in establishing the muscle phenotype. In teleosts, water temperature markedly affects embryonic development and larval growth. It has been previously shown that higher embryonic temperatures promoted faster development and increased size of Senegalese sole (Solea senegalensis) larvae relatively to a lower temperature. The role of miRNAs in thermal-plasticity of growth is hitherto unknown. Hence, we have used high-throughput SOLiD sequencing to determine potential changes in the miRNA transcriptome in Senegalese sole embryos that were incubated at 15°C or 21°C until hatching and then reared at a common temperature of 21°C.

Results: We have identified 320 conserved miRNAs in Senegalese sole, of which 48 had not been previously described in teleosts. mir-17a-5p, mir-26a, mir-130c, mir-206-3p, mir-181a-5p, mir-181a-3p and mir-199a-5p expression levels were further validated by RT- qPCR. The majority of miRNAs were dynamically expressed during early development, with peaks of expression at pre-metamorphosis or metamorphosis. Also, a higher incubation temperature (21°C) was associated with expression of some miRNAs positively related with growth (e.g., miR-17a, miR-181-5p and miR-206) during segmentation and at hatching. Target prediction revealed that these miRNAs may regulate myogenesis through MAPK and mTOR pathways. Expression of miRNAs involved in lipid metabolism and energy production (e.g., miR-122) also differed between temperatures. A miRNA that can potentially target calpain (miR-181-3p), and therefore negatively regulate myogenesis, was preferentially expressed during segmentation at 15°C compared to 21°C.

Conclusions: Temperature has a strong influence on expression of miRNAs during embryonic and larval development in fish. Higher expression levels of miR-17a, miR-181-5p and miR-206-3p and down-regulation of miR-181a-3p at 21°C may promote myogenesis and are in agreement with previous studies in Senegalese sole, which reported enhanced growth at higher embryonic temperatures compared to 15°C. Moreover, miRNAs involved in lipid metabolism and energy production may also contribute to increased larval growth at 21°C compared to 15°C. Taken together, our data indicate that miRNAs may play a role in temperature-induced phenotypic plasticity of growth in teleosts.

Citing Articles

Integration of mRNA and miRNA Analysis Sheds New Light on the Muscle Response to Heat Stress in Spotted Sea Bass ().

Liu C, Wen H, Zheng Y, Zhang C, Zhang Y, Wang L Int J Mol Sci. 2024; 25(22).

PMID: 39596165 PMC: 11594061. DOI: 10.3390/ijms252212098.


Embryonic temperature has long-term effects on muscle circRNA expression and somatic growth in Nile tilapia.

Rbbani G, Murshed R, Siriyappagouder P, Sharko F, Nedoluzhko A, Joshi R Front Cell Dev Biol. 2024; 12:1369758.

PMID: 39149515 PMC: 11324953. DOI: 10.3389/fcell.2024.1369758.


Are fish immunocompetent enough to face climate change?.

Franke A, Beemelmanns A, Miest J Biol Lett. 2024; 20(2):20230346.

PMID: 38378140 PMC: 10878809. DOI: 10.1098/rsbl.2023.0346.


Plasma cortisol and production of miRNAs in red drum (Sciaenops ocellatus) exposed to three distinct challenges.

Houdelet C, Blondeau-Bidet E, Mialhe X, Lallement S, Devilliers S, Falguiere J Fish Physiol Biochem. 2024; 50(2):757-766.

PMID: 38265685 DOI: 10.1007/s10695-024-01304-x.


The Discovery and Characterization of Conserved and Novel miRNAs in the Different Developmental Stages and Organs of Pikeperch ().

Verleih M, Visnovska T, Nguinkal J, Rebl A, Goldammer T, Andreassen R Int J Mol Sci. 2024; 25(1).

PMID: 38203361 PMC: 10778745. DOI: 10.3390/ijms25010189.


References
1.
Chang T, Mendell J . microRNAs in vertebrate physiology and human disease. Annu Rev Genomics Hum Genet. 2007; 8:215-39. DOI: 10.1146/annurev.genom.8.080706.092351. View

2.
Xie C, Xu S, Yang L, Ke Z, Xing J, Gai J . mRNA/microRNA Profile at the Metamorphic Stage of Olive Flounder (Paralichthys olivaceus). Comp Funct Genomics. 2011; 2011:256038. PMC: 3092494. DOI: 10.1155/2011/256038. View

3.
Juan A, Kumar R, Marx J, Young R, Sartorelli V . Mir-214-dependent regulation of the polycomb protein Ezh2 in skeletal muscle and embryonic stem cells. Mol Cell. 2009; 36(1):61-74. PMC: 2761245. DOI: 10.1016/j.molcel.2009.08.008. View

4.
Ren H, Accili D, Duan C . Hypoxia converts the myogenic action of insulin-like growth factors into mitogenic action by differentially regulating multiple signaling pathways. Proc Natl Acad Sci U S A. 2010; 107(13):5857-62. PMC: 2851893. DOI: 10.1073/pnas.0909570107. View

5.
Bizuayehu T, Lanes C, Furmanek T, Karlsen B, Fernandes J, Johansen S . Differential expression patterns of conserved miRNAs and isomiRs during Atlantic halibut development. BMC Genomics. 2012; 13:11. PMC: 3398304. DOI: 10.1186/1471-2164-13-11. View