cDNA cloning and chromosomal mapping of a novel human GAP (GAP1M), a GTPase-activating protein of Ras

Genomics. 1996 Aug 1;35(3):625-7. doi: 10.1006/geno.1996.0412.

Abstract

We have previously isolated a novel Ras GTPase-activating protein (Ras GAP), Gap1m, from rat brain. Gap1m is considered to be a negative regulator of the Ras signaling pathways, like other Ras GAPs, neurofibromin, which is a gene product of the neurofibromatosis type I gene, and p120GAP. In this study we have isolated a human cDNA of this Gap and mapped the gene. The gene encodes a protein of 853 amino acids that shows 89% sequence identity to rat Gap1m. The human gene was mapped to chromosome 3 by PCR analysis on a panel of human-mouse hybrid cells. FISH analysis refined the location of the gene further to 3q22-q23.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell Line
  • Chromosome Mapping
  • Chromosomes, Human, Pair 3*
  • Cloning, Molecular
  • DNA, Complementary
  • GTPase-Activating Proteins
  • Humans
  • Hybrid Cells
  • In Situ Hybridization, Fluorescence
  • Mice
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Proteins / genetics*
  • Rats
  • Sequence Homology, Amino Acid
  • ras GTPase-Activating Proteins
  • ras Proteins / metabolism*

Substances

  • DNA, Complementary
  • GTPase-Activating Proteins
  • Proteins
  • ras GTPase-Activating Proteins
  • ras Proteins

Associated data

  • GENBANK/D82880
  • GENBANK/D82881