Genomic and functional characterization of the lect2 gene from Siniperca chuatsi.
Amino Acid Sequence
Animals
Base Sequence
Fish Diseases
/ immunology
Fish Proteins
/ chemistry
Gene Expression Profiling
/ veterinary
Gene Expression Regulation
/ immunology
Immunity, Innate
/ genetics
Intercellular Signaling Peptides and Proteins
/ chemistry
Perciformes
/ genetics
Phylogeny
Protein Structure, Tertiary
Sequence Alignment
/ veterinary
DNA methylation
Leukocyte cell-derived chemotaxin 2
Liver
Siniperca chuatsi
miR-145–3p
Journal
Fish & shellfish immunology
ISSN: 1095-9947
Titre abrégé: Fish Shellfish Immunol
Pays: England
ID NLM: 9505220
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
08
05
2020
revised:
09
08
2020
accepted:
26
09
2020
pubmed:
30
9
2020
medline:
6
5
2021
entrez:
29
9
2020
Statut:
ppublish
Résumé
Mandarin fish (Siniperca chuatsi) is an important economic fish in China. Viral and bacterial diseases seriously affect the artificial culture of S. chuatsi. As a carnivorous fish, artificial feed domestication is also an important means to improve the scale of S. chuatsi culture. Therefore, the study of immunology and digestive physiology is very important to the industrial development of S. chuatsi. In this work, we analyzed the expression and function of the S. chuatsi leukocyte cell-derived chemotaxin 2 (Sc-lect2) gene on a basis of next generation, single-molecule long-read sequencing. Sc-lect2 was mainly expressed in the liver but barely expressed in the gill, skin, muscle, kidney, head kidney, brain, stomach, and intestine. When the fish were infected with infectious spleen and kidney necrosis virus and challenged with lipopolysaccharide and polyinosinic-polycytidylic acid, Sc-lect2 expression significantly increased by about 40, 17, and 7-fold, respectively, compared with unstimulated samples. We also found that Sc-lect2 increases by approximately 8-fold after the fish are fed an artificial diet. These results show that mandarin fish liver can not only digest food but also express specific immune genes. Changes in the diet can cause the differential expression of Sc-lect2 genes. Four Sc-lect2 interaction genes were differentially expressed in the skin or blood. Interestingly, miR-145-3p could inhibit Sc-lect2 gene expression by targeting its coding sequence region. One CpG island in the promoter region showed a high level of methylation, suggesting that high methylation does not affect Sc-lect2 gene expression in the liver.
Identifiants
pubmed: 32991992
pii: S1050-4648(20)30657-4
doi: 10.1016/j.fsi.2020.09.034
pii:
doi:
Substances chimiques
Fish Proteins
0
Intercellular Signaling Peptides and Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
146-155Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.