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Science 16 July 1993: Vol. 261. no. 5119, pp. 355 - 358 DOI: 10.1126/science.8332900
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Articles
Science, Vol 261, Issue 5119, 355-358
Copyright © 1993 by American Association for the Advancement of Science
Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes
JD Thomas,
P Sideras,
CI Smith,
I Vorechovsky,
V Chapman,
and
WE Paul
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Mice that bear the X-linked immunodeficiency (xid) mutation have a B lymphocyte-specific defect resulting in an inability to make antibody responses to polysaccharide antigens. A backcross of 1114 progeny revealed the colocalization of xid with Bruton's agammaglobulinemia tyrosine kinase (btk) gene, which is implicated in the human immune deficiency, X-linked agammaglobulinemia. Mice that carry xid have a missense mutation that alters a highly conserved arginine near the amino-terminus of the btk protein, Btk. Because this region of Btk lies outside any obvious kinase domain, the xid mutation may define another aspect of tyrosine kinase function.
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