L-serine synthesis in the central nervous system: a review on serine deficiency disorders

Mol Genet Metab. 2010 Mar;99(3):256-62. doi: 10.1016/j.ymgme.2009.10.012. Epub 2009 Oct 25.

Abstract

The de novo synthesis of the amino acid L-serine plays an essential role in the development and functioning of the central nervous system (CNS). L-serine displays many metabolic functions during different developmental stages; among its functions providing precursors for amino acids, protein synthesis, nucleotide synthesis, neurotransmitter synthesis and L-serine derived lipids. Patients with congenital defects in the L-serine synthesizing enzymes present with severe neurological abnormalities and underscore the importance of this synthetic pathway. In this review, we will discuss the cellular functions of the L-serine pathway, structure and enzymatic properties of the enzymes involved and genetic defects associated with this pathway.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / genetics*
  • Animals
  • Brain / metabolism
  • Brain Diseases, Metabolic, Inborn / genetics
  • Central Nervous System / metabolism*
  • Humans
  • Mice
  • Mutation
  • Phosphoglycerate Dehydrogenase / deficiency
  • Phosphoglycerate Dehydrogenase / genetics
  • Phosphoric Monoester Hydrolases / deficiency
  • Phosphoric Monoester Hydrolases / genetics
  • Rats
  • Serine / biosynthesis*
  • Serine / deficiency*
  • Syndrome
  • Transaminases / deficiency
  • Transaminases / genetics

Substances

  • Serine
  • Phosphoglycerate Dehydrogenase
  • Transaminases
  • phosphoserine aminotransferase
  • Phosphoric Monoester Hydrolases
  • phosphoserine phosphatase