Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice

  • David J. Rawlings
  • , Douglas C. Saffran
  • , Satoshi Tsukada
  • , David A. Largaespada
  • , J. Christopher Grimaldi
  • , Lucie Cohen
  • , Randolph N. Mohr
  • , J. Fernando Bazan
  • , Maureen Howard
  • , Neal G. Copeland
  • , Nancy A. Jenkins
  • , Owen N. Witte

Research output: Contribution to journalArticlepeer-review

827 Scopus citations

Abstract

The cytoplasmic tyrosine kinase, Bruton's tyrosine kinase (Btk, formerly bpk or atk), is crucial for B cell development. Loss of kinase activity results in the human immunodeficiency, X-linked agammaglobulinemia, characterized by a failure to produce B cells. In the murine X-linked immunodeficiency (XID), B cells are present but respond abnormally to activating signals. The Btk gene, btk, was mapped to the xid region of the mouse X chromosome by interspecific backcross analysis. A single conserved residue within the amino terminal unique region of Btk was mutated in XID mice. This change in xid probably interferes with normal B cell signaling mediated by Btk protein interactions.

Original languageEnglish (US)
Pages (from-to)358-361
Number of pages4
JournalScience
Volume261
Issue number5119
StatePublished - Jul 16 1993
Externally publishedYes

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