Interaction cloning and characterization of the cDNA encoding the human prenylated rab acceptor (PRA1)

Biochem Biophys Res Commun. 1999 May 19;258(3):657-62. doi: 10.1006/bbrc.1999.0651.

Abstract

Rab proteins are small GTPases involved in the regulation of intracellular membrane traffic in mammalian cells. In order to find Rab-interacting proteins we performed a two-hybrid screening using a human brain cDNA library. Here we report the isolation of a full-length human cDNA clone coding for a protein of 185 amino acids. This protein interacts strongly with the Rab4b, Rab5a, and Rab5c proteins and weakly with Rab4a, Rab6, Rab7, Rab17, and Rab22 in the two-hybrid assay. Comparison with the Data Bank revealed that this clone represents the human homolog of the previously isolated rat Prenylated Rab Acceptor (rPRA1). Analysis of mRNA expression shows a single abundant mRNA of about 0.8 kb ubiquitously expressed. Western blot analysis of the overexpressed protein shows a band of the expected size equally distributed between cytosol and membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Cell Line
  • Cloning, Molecular
  • Cricetinae
  • DNA, Complementary
  • GTP-Binding Proteins
  • Humans
  • Membrane Proteins
  • Molecular Sequence Data
  • Rats
  • Sequence Homology, Amino Acid
  • Vesicular Transport Proteins

Substances

  • Carrier Proteins
  • DNA, Complementary
  • Membrane Proteins
  • Rabac1 protein, rat
  • Vesicular Transport Proteins
  • GTP-Binding Proteins
  • RABAC1 protein, human

Associated data

  • GENBANK/AJ133534