Oxygen sensing and transcriptional regulation under hypoxia exposure in the mollusk Crassostrea gigas.
Feedback loop
Hypoxia inducible factor
Hypoxia responsive element
Oyster
Prolyl-4-hydroxylase
Protein structure
Journal
The Science of the total environment
ISSN: 1879-1026
Titre abrégé: Sci Total Environ
Pays: Netherlands
ID NLM: 0330500
Informations de publication
Date de publication:
20 Dec 2022
20 Dec 2022
Historique:
received:
13
06
2022
revised:
23
08
2022
accepted:
01
09
2022
pubmed:
10
9
2022
medline:
28
10
2022
entrez:
9
9
2022
Statut:
ppublish
Résumé
Hypoxia caused by global climate change and anthropogenic pollution has exposed marine species to increasing stress. Oxygen sensing mediated by prolyl hydroxylase (PHD) is regarded as the first line of defense under hypoxia exposure; however, the function of PHD in marine molluscan species remains unclear. In this study, we identified two PHD2 gene in the oyster Crassostrea gigas using phylogenetic tree analysis with 36 species, namely, CgPHD2A/B. Under hypoxia, the mRNA and protein expression of CgPHD2A displayed a time-dependent pattern, revealing a critical role in the response to hypoxia-induced stress. Observation of interactions between CgPHD2 and CgHIF-1α proteins under normoxia using co-immunoprecipitation and GST-pull down experiments showed that the β2β3 loop in CgPHD2A hydroxylates CgHIF-1α to promote its ubiquitination with CgVHL. With the protein recombination and site-directed mutagenesis, the hydroxylation domain and two target proline loci (P404A and 504A) in CgPHDs and CgHIF-1α were identified respectively. Moreover, the electrophoretic mobility-shift assay (EMSA) and luciferase double reporter gene assay revelaed that CgHIF-1α could regulate CgPHD2A expression through binding with the hypoxia-responsive element in the promoter region (320 bp upstream), forming a feedback loop. However, protein structure analysis indicated that six extra amino acids formed an α-helix in the β2β3 loop of CgPHD2B, inhibiting its activity. Overall, this study revealed that two CgPHD2 proteins have evolved, which encode enzymes with different activities in oyster, potentially representing a specific hypoxia-sensing mechanism in mollusks. Illustrating the functional diversity of CgPHDs could help to assess the physiological status of oyster and guide their aquaculture.
Identifiants
pubmed: 36084780
pii: S0048-9697(22)05656-X
doi: 10.1016/j.scitotenv.2022.158557
pii:
doi:
Substances chimiques
Oxygen
S88TT14065
Procollagen-Proline Dioxygenase
EC 1.14.11.2
RNA, Messenger
0
Proline
9DLQ4CIU6V
Amino Acids
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
158557Informations de copyright
Copyright © 2022. Published by Elsevier B.V.
Déclaration de conflit d'intérêts
Declaration of competing interest There is no conflict of interest in the manuscript, which is approved by all authors for publication. We also declare that the work described is original research that has not been published previously, and not under consideration for publication elsewhere, in whole or in part.