Vu T H, Begovich A B, Tacchini-Cottier F M, Jones P P
Department of Biological Sciences, Stanford University, CA 94305-5020.
J Immunol. 1989 Apr 15;142(8):2936-42.
The expression and sequences of the mouse MHC class II genes, E alpha f and E alpha q, have been studied to determine the molecular basis for their defective expression. Previous work in our laboratory showed that H-2f and H-2q mice produce no detectable E alpha protein. Northern blot analysis confirms previous results showing normal amounts of E alpha f message and a 100-fold reduction in E alpha q mRNA. Despite that observation, the rates of transcription of both defective E alpha genes, measured by nuclear run-on transcription assays, are comparable to that of the normally expressed E alpha k gene. The nucleotide sequences of the E alpha f and E alpha q genes reveal mutations generating premature translation stop codons in both genes. A single base substitution has created the stop codon TGA at amino acid -2 in the E alpha f leader sequence. A nucleotide insertion at codon 64 in the second exon of the E alpha q gene results in a frame shift and a premature stop codon at amino acid residue 69 of a mature E alpha protein. The low steady state level of E alpha q mRNA may be correlated with the unusual size distribution of the RNA, possibly due to altered RNA processing.
对小鼠MHC II类基因Eαf和Eαq的表达及序列进行了研究,以确定其表达缺陷的分子基础。我们实验室之前的研究表明,H-2f和H-2q小鼠无法产生可检测到的Eα蛋白。Northern印迹分析证实了之前的结果,即Eαf信使RNA量正常,而Eαq mRNA减少了100倍。尽管有此观察结果,但通过核转录分析测定的两个缺陷Eα基因的转录速率与正常表达的Eαk基因相当。Eαf和Eαq基因的核苷酸序列显示,两个基因中均发生了产生过早翻译终止密码子的突变。一个单碱基替换在Eαf前导序列的第-2位氨基酸处产生了终止密码子TGA。Eαq基因第二个外显子的第64位密码子处的核苷酸插入导致移码,并在成熟Eα蛋白的第69位氨基酸残基处产生过早的终止密码子。Eαq mRNA的低稳态水平可能与RNA异常的大小分布相关,这可能是由于RNA加工改变所致。