Isolation and characterization of a novel HS1 SH3 domain binding protein, HS1BP3

Int Immunol. 1999 Dec;11(12):1957-64. doi: 10.1093/intimm/11.12.1957.

Abstract

We have isolated a novel gene, HS1BP3, which encodes an HS1 binding protein. Analysis of HS1BP3 cDNA indicates several potentially important segments, including a PX domain, a leucine zipper, immunoreceptor tyrosine-based inhibitory motif-like motifs and proline-rich regions. HS1BP3 associates with HS1 proteins in vivo as confirmed by immunoprecipitation in B and T cell lines. HS1BP3 preferentially associates with the HS1 SH3 domains rather than with other SH3 molecules, suggesting a role of HS1BP3 as an HS1 signaling mediator. Overexpression of mutant HS1BP3 protein in T cell lines results in decreased IL-2 production. Our data suggest a novel role for HS1BP3 in lymphocyte activation.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Blood Proteins / metabolism*
  • Carrier Proteins / chemistry
  • Carrier Proteins / isolation & purification*
  • Carrier Proteins / physiology
  • Cell Line
  • Interleukin-2 / biosynthesis
  • Lymphocyte Activation
  • Mice
  • Molecular Sequence Data
  • src Homology Domains*

Substances

  • Adaptor Proteins, Signal Transducing
  • Blood Proteins
  • Carrier Proteins
  • HCLS1 protein, human
  • Interleukin-2

Associated data

  • GENBANK/AJ132192