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RNA-seq analysis of the mantle transcriptome from Mytilus edulis during a seasonal spawning event in deep and shallow water culture sites on the northeast coast of Newfoundland, Canada.
Gallardi, Daria; Xue, Xi; Mercier, Eloi; Mills, Terry; Lefebvre, Francois; Rise, Matthew L; Murray, Harry M.
Affiliation
  • Gallardi D; Fisheries and Oceans Canada, 80 East White Hills Road, PO Box 5667, St. John's, NL A1C 5X1, Canada. Electronic address: daria.gallardi@dfo-mpo.gc.ca.
  • Xue X; Department of Ocean Sciences, Memorial University of Newfoundland, St. John's, NL A1C 5S7, Canada.
  • Mercier E; Canadian Centre for Computational Genomics - Montreal Node, McGill University and Genome Quebec Innovation Center, 740 Dr. Penfield Avenue, Montréal, Québec H3A 0G1, Canada.
  • Mills T; Norlantic Processors Limited, P.O. Box 381, Botwood, NL A0H 1E0, Canada.
  • Lefebvre F; Canadian Centre for Computational Genomics - Montreal Node, McGill University and Genome Quebec Innovation Center, 740 Dr. Penfield Avenue, Montréal, Québec H3A 0G1, Canada.
  • Rise ML; Department of Ocean Sciences, Memorial University of Newfoundland, St. John's, NL A1C 5S7, Canada.
  • Murray HM; Fisheries and Oceans Canada, 80 East White Hills Road, PO Box 5667, St. John's, NL A1C 5X1, Canada.
Mar Genomics ; 60: 100865, 2021 Dec.
Article in En | MEDLINE | ID: mdl-33933383
ABSTRACT
The blue mussel (Mytilus edulis) has global commercial and ecological importance both in wild and cultured conditions. However there is a qualitative and quantitative lack of knowledge of the molecular mechanisms associated with its reproductive physiology, especially with reference to environmental interactions. Here we initiated a transcriptomic analysis (RNA-sequencing (RNA-seq)) of the mantle from both sexes sampled during a seasonal spawning event and from two culture depths (shallow-5 m; deep- 15 m). Mantle libraries were produced from 3 males and 3 females sampled from each of two shallow sites and two deep sites for a total of 12 replicate male and 12 replicate female libraries (24 total libraries). Overall a total of 2.3 billion raw 100 base reads with an average of 96.5 million reads/library were obtained and assembled into 296,118 transcripts with an average length of 568 bp. Overall, 315 transcripts from male libraries and 25 from female libraries were found to be upregulated in deep water as compared to shallow (edgeR adjusted p value ≤ 0.05). Conversely, 126 transcripts from male libraries and 135 from female libraries were found to be significantly downregulated at the same depth. Thirteen transcripts were selected for qPCR validation based on importance in reproduction, antimicrobial defense and metabolism. Of these, 9 RNA-seq identified transcripts were shown by qPCR to be differentially expressed between groups 2 were upregulated in deep compared with shallow water (dhx38, mt-co1), 2 were upregulated for female compared with male mantle (pias2, mapkap1) and 6 genes (fndc3a, acbd3, klhl10, ccnb3, armc4, mt-co1) showed to be upregulated in males compared to females. The majority of qPCR studied transcripts were identified as involved in gamete development based on the UniProt database. This study further characterizes the importance of the mantle transcriptome during reproductive activities of M. edulis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mytilus edulis Type of study: Qualitative_research Limits: Animals Country/Region as subject: America do norte Language: En Journal: Mar Genomics Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mytilus edulis Type of study: Qualitative_research Limits: Animals Country/Region as subject: America do norte Language: En Journal: Mar Genomics Year: 2021 Document type: Article
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