Comparative proteomics and transcriptomics illustrate the allograft-induced stress response in the pearl oyster (Pinctada fucata martensii).


Journal

Fish & shellfish immunology
ISSN: 1095-9947
Titre abrégé: Fish Shellfish Immunol
Pays: England
ID NLM: 9505220

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 10 08 2021
revised: 23 12 2021
accepted: 29 12 2021
pubmed: 7 1 2022
medline: 16 3 2022
entrez: 6 1 2022
Statut: ppublish

Résumé

Implantation of a spherical nucleus into a recipient oyster is a critical step in artificial pearl production. However, the molecular mechanisms underlying the response of the pearl oyster to this operation are poorly understood. In this research, we used transcriptomic and proteomic analyses to examine allograft-induced changes in gene/protein expression patterns in Pinctada fucata martensii 12 h after nucleus implantation. Transcriptome analysis identified 688 differential expression genes (DEGs) (FDR<0.01 and |fold change) > 2). Using a 1.2-fold increase or decrease in protein expression as a benchmark for differentially expressed proteins (DEPs), 108 DEPs were reliably quantified, including 71 up-regulated proteins (DUPs) and 37 down-regulated proteins (DDPs). Further analysis revealed that the GO terms, including "cellular process", "biological regulation" and "metabolic process" were considerably enriched. In addition, the transcriptomics analysis showed that "Neuroactive ligand-receptor interaction", "NF-kappa B signaling pathway", "MAPK signaling pathway", "PI3K-Akt signaling pathway', "Toll-like receptor signaling pathway", and "Notch signaling pathway" were significantly enriched in DEGs. The proteomics analysis showed that "ECM-receptor interaction", "Human papillomavirus infection", and "PI3K-Akt signaling pathway" were significantly enriched in DEPs. The results indicate that these functions could play an important role in response to pear oyster stress at nucleus implantation. To assess the potential relevance of quantitative information between mRNA and proteins, using Ward's hierarchical clustering analysis clustered the protein/gene expression patterns across the experimental and control samples into six groups. To investigate the biological processes associated with the protein in each cluster, we identified the significantly enriched GO terms and KEGG pathways in the proteins in each cluster. Gene set enrichment analysis (GSEA) was used to reveal the potential protein or transcription pathways associated with the response to nuclear implantation. Thus, the study of P. f. martensii is essential to enhance our understanding of the molecular mechanisms involved in pearl biosynthesis and the biology of bivalve molluscs.

Identifiants

pubmed: 34990804
pii: S1050-4648(21)00471-X
doi: 10.1016/j.fsi.2021.12.055
pii:
doi:

Substances chimiques

Proto-Oncogene Proteins c-akt EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

74-85

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

Jinzhao Lu (J)

Fisheries College of Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.

Meizhen Zhang (M)

Fisheries College of Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.

Haiying Liang (H)

Fisheries College of Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China; Guangdong Provincial Key Laboratory of Pathogenic Biology and Epidemiology for Aquatic Economic Animals, Zhanjiang, Guangdong, 524088, China. Electronic address: zjlianghy@126.com.

Chenghao Shen (C)

Fisheries College of Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.

Bin Zhang (B)

Fisheries College of Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.

Bidan Liang (B)

Fisheries College of Guangdong Ocean University, Zhanjiang, Guangdong, 524088, China.

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Classifications MeSH