Determination of the primary structure of PLC-154 demonstrates diversity of phosphoinositide-specific phospholipase C activities

Cell. 1988 Jul 15;54(2):171-7. doi: 10.1016/0092-8674(88)90549-1.

Abstract

Protein sequence analysis of a bovine brain phosphoinositide-specific phospholipase C (PI-PLC; PLC-154) has permitted the isolation of a cDNA that appears to code for this protein. Transient expression of this cDNA in COS-1 cells demonstrates that the cDNA encodes a functional phospholipase C that migrates at approximately 150,000 daltons. A transcript of approximately 7 kb is observed in RNA derived from bovine brain and a related transcript of the same size is present in certain human cell lines. Southern blot analysis indicates that one or possibly two genes hybridize with a PLC-154 probe. Regions of homology between PLC-154 and the previously described PLC-148 allow the assignment of a putative catalytic domain to the central region of PLC-154.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Brain / enzymology*
  • Cattle
  • Cell Line
  • Cloning, Molecular
  • DNA / biosynthesis
  • DNA / genetics
  • Electrophoresis, Polyacrylamide Gel
  • Gene Expression Regulation
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Phosphatidylinositols / metabolism*
  • RNA / genetics
  • Sequence Homology, Nucleic Acid
  • Substrate Specificity
  • Transcription, Genetic
  • Type C Phospholipases / genetics*
  • Type C Phospholipases / metabolism

Substances

  • Phosphatidylinositols
  • RNA
  • DNA
  • Type C Phospholipases

Associated data

  • GENBANK/J03137