Rawlings D J, Saffran D C, Tsukada S, Largaespada D A, Grimaldi J C, Cohen L, Mohr R N, Bazan J F, Howard M, Copeland N G
Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024.
Science. 1993 Jul 16;261(5119):358-61. doi: 10.1126/science.8332901.
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.
细胞质酪氨酸激酶,布鲁顿酪氨酸激酶(Btk,以前称为bpk或atk),对B细胞发育至关重要。激酶活性丧失会导致人类免疫缺陷疾病——X连锁无丙种球蛋白血症,其特征是无法产生B细胞。在小鼠X连锁免疫缺陷(XID)中,B细胞存在,但对激活信号反应异常。通过种间回交分析,将Btk基因(btk)定位到小鼠X染色体的xid区域。XID小鼠中,Btk氨基末端独特区域内的一个保守残基发生了突变。xid中的这种变化可能会干扰由Btk蛋白相互作用介导的正常B细胞信号传导。