Dorn A, Durand B, Marfing C, Le Meur M, Benoist C, Mathis D
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6249-53. doi: 10.1073/pnas.84.17.6249.
A conserved sequence motif exists at the 5' end of all major histocompatibility complex class II genes. This motif consists of the 14-base X and Y boxes separated by a short stretch of variable sequence. In this report, we provide evidence that the X and Y boxes play an important role in controlling transcription of the murine class II gene E kappa alpha. We have developed transgenic mouse lines that carry E alpha genes cleanly deleted for either the X or Y box and have compared the expression of these mutant transgenes with that of a nondeleted control. Both the X and Y segments appear critical for accurate and efficient transcription of E kappa alpha. The most drastic effect is seen with gamma-interferon-treated macrophages, where deletion of the Y box completely abrogates transcription initiated by the normal promoter. In addition, we identify proteins from nuclear extracts that bind specifically to the X or Y box.
在所有主要组织相容性复合体II类基因的5'端存在一个保守的序列基序。该基序由14个碱基的X盒和Y盒组成,中间间隔一段短的可变序列。在本报告中,我们提供证据表明X盒和Y盒在控制小鼠II类基因Eκα的转录中起重要作用。我们构建了携带X盒或Y盒被完全缺失的Eα基因的转基因小鼠品系,并将这些突变转基因的表达与未缺失的对照进行了比较。X和Y片段对于Eκα的准确和高效转录似乎都至关重要。在γ干扰素处理的巨噬细胞中观察到最显著的影响,其中Y盒的缺失完全消除了正常启动子启动的转录。此外,我们鉴定了来自核提取物中与X盒或Y盒特异性结合的蛋白质。