Involvement of CgPGC-1α in regulating mitochondrial biogenesis in Pacific oyster Crassostrea gigas under ocean acidification

Highlights

  • CgPGC-1α with classical RRM domain was identified from Crassostrea gigas.
  • CgPGC-1α mRNA was ubiquitously expressed with the highest level in gill.
  • CgPGC-1α could respond to acidification treatment, promote mitochondrial biogenesis.
  • Acidification enhanced mitochondrial biogenesis and ATP via AMPKα/PGC-1α.

Abstract

Ocean acidification poses a significant threat to calcifying marine organisms. The Pacific oyster Crassostrea gigas is an economically and ecologically important bivalve species. Understanding the molecular mechanisms underlying its physiological adaptation to acidification stress is therefore of great ecological and aquaculture relevance. Peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) is a central regulator of mitochondrial biogenesis and cellular energy metabolism, which plays important roles in response to various stressors. In this study, a PGC-1α homolog was identified from Crassostrea gigas (CgPGC-1α), which harbors an evolutionarily conserved RRM domain. The phylogenetic tree indicated that CgPGC-1α first clustered with PGC-1α from molluscs, then grouped with vertebrate PGC-1α, and finally joined with the PGC-1α of arthropods. During larval development, expression level of CgPGC-1α increased from the early embryonic stages, reached its highest level at blastula stage, and subsequently decreased during later development stages. In adult oysters, expression level of CgPGC-1α were detected in haemocytes and all examined tissues, with the highest level in gills. When the oysters were exposed to acidified seawater at pH 7.4, the expression level of CgPGC-1α in gonad was significantly upregulated at 7 and 21 days. Furthermore, at 7 days after acidification treatment, the mtDNA copy number, the expression level of CgMFN mRNA transcripts, the CgPGC-1α protein levels and the pAMPKα (Thr172) phosphorylation levels all significantly increased (p < 0.05), while the relative mRNA expression level of CgDRP1 significantly decreased (p < 0.05). Moreover, a significant increase in the number of mitochondria with morphology changing from elliptical to irregular and cristae becoming swollen was observed, and the ATP content was significantly elevated. After 28d days of acidification, mtDNA copy number and the expression level of CgMFN and CgNRF2 were significantly decreased, whereas the expression level of CgDRP1 was significantly increased. Collectively, these findings reveal a temporal response to acidification, characterized by an early compensatory activation of the AMPKα/PGC-1α axis and enhanced mitochondrial biogenesis, followed by impaired mitochondrial homeostasis under prolonged acidification stress. This study provides new insights into the molecular mechanisms underlying oyster resilience to ocean acidification and highlights the potential importance of mitochondrial adaptation in coping with future environmental changes.

Jiang D., Lu H., Zhang Z., Yang C., Liu C., Wang L. & Song L., 2026. Involvement of CgPGC-1α in regulating mitochondrial biogenesis in Pacific oyster Crassostrea gigas under ocean acidification. Comparative Immunology Reports 11: 200308. doi: 10.1016/j.cirep.2026.200308. Article.


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