PYP-1, inorganic pyrophosphatase, is required for larval development and intestinal function in C. elegans

FEBS Lett. 2007 Nov 27;581(28):5445-53. doi: 10.1016/j.febslet.2007.10.047. Epub 2007 Nov 5.

Abstract

Inorganic pyrophosphatase (PPase) catalyzes the hydrolysis of inorganic pyrophosphate (PPi) into phosphate (Pi), which provides a thermodynamic driving force for important biosynthetic reactions. The nematode Caenorhabditis elegans gene C47E12.4 encodes a PPase (PYP-1) which shows 54% amino acid identity with human PPase. PYP-1 exhibits specific enzyme activity and is mainly expressed in the intestinal and nervous system. A null mutant of pyp-1 reveals a developmental arrest at early larval stages and exhibits gross defects in intestinal morphology and function. The larval arrest phenotype was successfully rescued by reintroduction of the pyp-1 gene, suggesting that PYP-1 is required for larval development and intestinal function in C. elegans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / growth & development*
  • Caenorhabditis elegans / metabolism*
  • Conserved Sequence
  • Gene Deletion
  • Gene Expression Regulation, Developmental*
  • Gene Expression Regulation, Enzymologic*
  • Humans
  • Inorganic Pyrophosphatase / chemistry
  • Inorganic Pyrophosphatase / genetics
  • Inorganic Pyrophosphatase / metabolism*
  • Intestines / enzymology*
  • Intestines / growth & development*
  • Molecular Sequence Data
  • Mutation / genetics
  • Phenotype
  • Sequence Alignment

Substances

  • Inorganic Pyrophosphatase