首页> 美国卫生研究院文献>Genetics >An allelic series of mutations in the kit ligand gene of mice. I. Identification of point mutations in seven ethylnitrosourea-induced Kitl(Steel) alleles.
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An allelic series of mutations in the kit ligand gene of mice. I. Identification of point mutations in seven ethylnitrosourea-induced Kitl(Steel) alleles.

机译:小鼠试剂盒配体基因中的等位基因系列突变。 I.鉴定七个乙基亚硝基脲诱导的Kitl(Steel)等位基因中的点突变。

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摘要

An allelic series of mutations is an extremely valuable genetic resource for understanding gene function. Here we describe eight mutant alleles at the Steel (Sl) locus of mice that were induced with N-ethyl-N-nitrosourea (ENU). The product of the Sl locus is Kit ligand (or Kitl; also known as mast cell growth factor, stem cell factor, and Steel factor), which is a member of the helical cytokine superfamily and is the ligand for the Kit receptor tyrosine kinase. Seven of the eight ENU-induced Kitl(Sl) alleles, of which five cause missense mutations, one causes a nonsense mutation and exon skipping, and one affects a splice site, were found to contain point mutations in Kitl. Interestingly, each of the five missense mutations affects residues that are within, or very near, conserved alpha-helical domains of Kitl. These ENU-induced mutants should provide important information on structural requirements for function of Kitl and other helical cytokines.
机译:等位基因突变系列是了解基因功能的极有价值的遗传资源。在这里,我们描述了在小鼠的钢(Sl)基因座上由N-乙基-N-亚硝基脲(ENU)诱导的八个突变等位基因。 S1基因座的产物是Kit配体(或Kit1;也称为肥大细胞生长因子,干细胞因子和Steel因子),其是螺旋细胞因子超家族的成员,并且是Kit受体酪氨酸激酶的配体。在八个ENU诱导的Kit1(S1)等位基因中,有七个(其中五个引起错义突变,一个导致无义突变和外显子跳跃),另一个影响剪接位点,在Kitl中包含点突变。有趣的是,五个错义突变中的每一个都会影响Kit1的保守α-螺旋结构域内或附近的残基。这些ENU诱导的突变体应提供有关Kit1和其他螺旋细胞因子功能的结构要求的重要信息。

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