NADK-mediated proline synthesis enhances high-salinity tolerance in the razor clam

Comp Biochem Physiol A Mol Integr Physiol. 2024 May:291:111610. doi: 10.1016/j.cbpa.2024.111610. Epub 2024 Feb 24.

Abstract

Euryhaline organisms can accumulate organic osmolytes to maintain osmotic balance between their internal and external environments. Proline is a pivotal organic small molecule and plays an important role in osmoregulation that enables marine shellfish to tolerate high-salinity conditions. During high-salinity challenge, NAD kinase (NADK) is involved in de novo synthesis of NADP(H) in living organisms, which serves as a reducing agent for the biosynthetic reactions. However, the role of shellfish NADK in proline biosynthesis remains elusive. In this study, we show the modulation of NADK on proline synthesis in the razor clam (Sinonovacula constricta) in response to osmotic stress. Under acute hypersaline conditions, gill tissues exhibited a significant increase in the expression of ScNADK. To elucidate the role of ScNADK in proline biosynthesis, we performed dsRNA interference in the expression of ScNADK in gill tissues to assess proline content and the expression levels of key enzyme genes involved in proline biosynthesis. The results indicate that the knock-down of ScNADK led to a significant decrease in proline content (P<0.01), as well as the expression levels of two proline synthetase genes P5CS and P5CR involved in the glutamate pathway. Razor clams preferred to use ornithine as substrate for proline synthesis when the glutamate pathway is blocked. Exogenous administration of proline greatly improved cell viability and mitigated cell apoptosis in gills. In conclusion, our results demonstrate the important role of ScNADK in augmenting proline production under high-salinity stress, by which the razor clam is able to accommodate salinity variations in the ecological niche.

Keywords: Euryhaline; NADK; Osmolytes; Proline; Sinonovacula constricta.

MeSH terms

  • Animals
  • Bivalvia* / metabolism
  • Glutamates / metabolism
  • Phosphotransferases (Alcohol Group Acceptor)*
  • Proline / metabolism
  • Salt Tolerance*

Substances

  • NAD kinase
  • Proline
  • Glutamates
  • Phosphotransferases (Alcohol Group Acceptor)