Tsui H W, Siminovitch K A, de Souza L, Tsui F W
Toronto Hospital, Ontario, Canada.
Nat Genet. 1993 Jun;4(2):124-9. doi: 10.1038/ng0693-124.
Mice with the recessive motheaten (me) or the allelic viable motheaten (mev) mutations express a severe autoimmune and immunodeficiency syndrome. We have shown that the basic defect in these mice involves lesions in the gene which encodes haematopoietic cell phosphatase (HCP). These mice thus provide excellent models for investigating the roles of phosphatases in haematopoiesis and the nature of the genetic and cellular events linking impaired haematopoiesis to severe immunodeficiency and expression of systemic autoimmunity.
具有隐性食母生(me)或等位基因存活食母生(mev)突变的小鼠表现出严重的自身免疫和免疫缺陷综合征。我们已经表明,这些小鼠的基本缺陷涉及编码造血细胞磷酸酶(HCP)的基因中的损伤。因此,这些小鼠为研究磷酸酶在造血中的作用以及将造血受损与严重免疫缺陷和全身自身免疫表达联系起来的遗传和细胞事件的性质提供了极好的模型。