首页> 外文OA文献 >The DNA-binding defect observed in major histocompatibility complex class II regulatory mutants concerns only one member of a family of complexes binding to the X boxes of class II promoters.
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The DNA-binding defect observed in major histocompatibility complex class II regulatory mutants concerns only one member of a family of complexes binding to the X boxes of class II promoters.

机译:在主要的组织相容性复合物II类调控突变体中观察到的DNA结合缺陷仅涉及与II类启动子X盒结合的复合物家族中的一个成员。

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摘要

The X box of major histocompatibility complex class II promoters is essential for proper expression of class II genes. Here we show that two distinct protein-DNA complexes (A and B), which exhibit similar binding characteristics and identical contact points on the X box, can be formed. This suggests the existence of a family of related X box-binding factors. Complex B (and not complex A) is specifically affected in primary combined immunodeficiency, a congenital defect in class II gene regulation. RFX1, the first X box-binding protein cloned, encodes a functionally relevant factor present in complex A and not in complex B as originally suspected. This report also illustrates the need for caution in correlating specific cloned proteins with nuclear factors identified by DNA-binding assays, particularly when dealing with families of related proteins.
机译:主要组织相容性复合物II类启动子的X框对于II类基因的正确表达至关重要。在这里,我们表明可以形成两个不同的蛋白质-DNA复合物(A和B),它们表现出相似的结合特性和在X盒上相同的接触点。这表明存在一系列相关的X框结合因子。复合物B(而非复合物A)在原发性联合免疫缺陷(II类基因调节中的先天性缺陷)中受到特定影响。 RFX1是第一个克隆的X盒结合蛋白,它编码复合物A而不是最初怀疑的复合物B中存在的功能相关因子。该报告还说明在将特定克隆的蛋白质与通过DNA结合测定法鉴定的核因子相关联时需要谨慎,尤其是在处理相关蛋白质家族时。

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