Molecular cloning and function of two tumor necrosis factor receptor-associated factors genes (TRAF2 and TRAF4) from Pinctada fucata martensii
Tumor necrosis factor receptor-associated factors (TRAFs) have been studied in a few mollusks and participate in various biological processes, like apoptosis, immune response, stress, and inflammatory response. However, TRAFs’ function and mechanism of pearl oysters ( Pinctada fucata martensii ) are...
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Veröffentlicht in: | Frontiers in Marine Science 2023-01, Vol.9 |
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Sprache: | eng |
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Zusammenfassung: | Tumor necrosis factor receptor-associated factors (TRAFs) have been studied in a few mollusks and participate in various biological processes, like apoptosis, immune response, stress, and inflammatory response. However, TRAFs’ function and mechanism of pearl oysters (
Pinctada fucata martensii
) are still unclear. In this study, the novel
PmTRAF2
and
PmTRAF4
from
P. f. martensii
were cloned by rapid amplification of complementary DNA ends and their mRNA expression were analyzed by quantitative real-time PCR (qPCR). The interacting protein of PmTRAF2 was verified by the yeast two-hybrid assay. The result shows that full-length of
PmTRAF2
and
PmTRAF4
cDNA were 2055 bp and 2365 bp, respectively. The deduced PmTRAF2 and PmTRAF4 proteins contain TRAF-type zinc finger domain and MATH domain, while PmTRAF4 lacks a RING finger domain. Multiple sequence alignment revealed that PmTRAF2 and PmTRAF4 had high homology with the ortholog of other species. Phylogenic analysis indicated that PmTRAF4 clustered with the homolog protein of
Mytilus edulis
and
Mytilus galloprovincialis
, and PmTRAF2 has the closest genetic relationship to
Crassostrea gigas
TRAF2. The qPCR analysis revealed that
PmTRAF2
and
PmTRAF4
were expressed in all six tissues, and both of them were significantly expressed in hepatopancreas and gill (p < 0.01). Under lipopolysaccharide (LPS) stimulation, polyinosinic acid (PolyI:C) stimulation, and nucleus insertion surgery, the transcripts of
PmTRAF2
,
PmTRAF3
,
PmTRAF4
and
PmTRAF6
in hepatopancreas were markedly changed at corresponding time points. These results have indicated that these genes may play a role in
P. f. martensii
innate immunity. Yeast two-hybrid assays show that PmTRAF2 interacts with PmTRAF6 but not PmTRAF3, potentially affecting downstream immune signaling pathways. Our findings provide new perspectives for further investigation of TRAFs’ immune mechanisms in bivalves. |
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ISSN: | 2296-7745 2296-7745 |
DOI: | 10.3389/fmars.2022.1082975 |