Molecular characterization of Rab5A, and involvement in innate immunity in Yellow River Carp Cyprinus carpio
Rab5A play important roles in regulating trafficking organelles, especially in phagosome formation. In the present study, full-length cDNA sequences of Rab5A were cloned from Yellow River Carp Cyprinus carpio , which was designated as Cc Rab5A. The full-length cDNA of the Cc Rab5A cDNA sequence is 2...
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Veröffentlicht in: | Aquaculture international 2024-04, Vol.32 (2), p.1427-1451 |
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Zusammenfassung: | Rab5A play important roles in regulating trafficking organelles, especially in phagosome formation. In the present study, full-length cDNA sequences of Rab5A were cloned from Yellow River Carp
Cyprinus carpio
, which was designated as
Cc
Rab5A. The full-length cDNA of the
Cc
Rab5A cDNA sequence is 2434 bp and included an open reading frame (ORF) encoding 216 amino acids polypeptide with an estimated molecular weight of 23.47 kDa. Bioinformatics analysis showed that the
Cc
Rab5A protein was highly conserved during evolution.
Cc
Rab5A's deduced amino acid sequence showed high identity to
Cyprinus carpio
(99.54%) in comparison. The guanine-base binding motif (G), phosphate/magnesium-binding motif (PM), and Rab family motif (Rab F) of
Cc
Rab5A are highly conserved among various species, but the N- and C-terminal regions were hypervariable, according to the results of multiple sequence alignment and phylogenetic analysis. Additionally, 11 tissues of Yellow River Carp were examined using Real-time Fluorescence Quantitative PCR (qRT-PCR) to determine the expression levels, with the highest expression levels in head kidney and blood. Followed by heart, liver, muscle, brain, gill, skin, spleen and intestine; The expression level in body kidney was the lowest. Yellow River Carp was immunized with
Aeromonas hydrophila
and Spring viremia of carp virus (SVCV) respectively, and the expression changes of
Cc
Rab5A in gill, spleen, liver, intestine and skin of Yellow River Carp were detected. The results showed that the expression level of the gene was obviously up-regulated at different time points. The eukaryotic recombinant plasmids of
Cc
Rab5A, pEGFP-N3 were constructed and transfected into GCO cells for subcellular localization. The results showed that
Cc
Rab5A were mainly distributed in nuclear membrane and various endosome membranes. These results showed that
Cc
Rab5 were involved in viral and bacterial infection in the immune response of Yellow River Carp
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ISSN: | 0967-6120 1573-143X |
DOI: | 10.1007/s10499-023-01223-3 |