Arabidopsis mutants lacking long chain base phosphate lyase are fumonisin-sensitive and accumulate trihydroxy-18:1 long chain base phosphate

J Biol Chem. 2007 Sep 21;282(38):28195-206. doi: 10.1074/jbc.M705074200. Epub 2007 Jul 16.

Abstract

The sphingoid long chain bases (LCBs) and their phosphorylated derivatives (LCB-Ps) are important signaling molecules in eukaryotic organisms. The cellular levels of LCB-Ps are tightly controlled by the coordinated action of the LCB kinase activity responsible for their synthesis and the LCB-P phosphatase and lyase activities responsible for their catabolism. Although recent studies have implicated LCB-Ps as regulatory molecules in plants, in comparison with yeast and mammals, much less is known about their metabolism and function in plants. To investigate the functions of LCB-Ps in plants, we have undertaken the identification and characterization of Arabidopsis genes that encode the enzymes of LCB-P metabolism. In this study the Arabidopsis At1g27980 gene was shown to encode the only detectable LCB-P lyase activity in Arabidopsis. The LCB-P lyase activity was characterized, and mutant plant lines lacking the lyase were generated and analyzed. Whereas in other organisms loss of LCB-P lyase activity is associated with accumulation of high levels of LCB/LCB-Ps and developmental abnormalities, the sphingolipid profiles of the mutant plants were remarkably similar to those of wild-type plants, and no developmental abnormalities were observed. Thus, these studies indicate that the lyase plays a minor role in maintenance of sphingolipid metabolism during normal plant development and growth. However, a clear role for the lyase was revealed upon perturbation of sphingolipid synthesis by treatment with the inhibitor of ceramide synthase, fumonisin B(1).

Publication types

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

MeSH terms

  • Aldehyde-Lyases / genetics*
  • Aldehyde-Lyases / physiology
  • Amino Acid Sequence
  • Arabidopsis / genetics*
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • Arabidopsis Proteins / physiology
  • Fumonisins / chemistry
  • Fumonisins / metabolism*
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal*
  • Gene Expression Regulation, Plant*
  • Microsomes / metabolism
  • Models, Chemical
  • Molecular Sequence Data
  • Mutation*
  • Phosphates*
  • Saccharomyces cerevisiae / metabolism
  • Sequence Homology, Amino Acid
  • Sphingolipids / chemistry

Substances

  • Arabidopsis Proteins
  • Fumonisins
  • Fungal Proteins
  • Phosphates
  • Sphingolipids
  • fumonisin B1
  • Aldehyde-Lyases
  • At1g27980 protein, Arabidopsis