Richter D, Niegemann E, Brendel M
Institut für Mikrobiologie der J.W. Goethe-Universität, Frankfurt/Main, FRG.
Mol Gen Genet. 1992 Jan;231(2):194-200. doi: 10.1007/BF00279791.
A 3.2 kb yeast DNA fragment containing the DNA interstrand cross-link-specific repair gene SNM1 has been sequenced. Two genes were identified. SNM1 has an open reading frame of 1983 bp and codes for a 661 amino acid protein. Hydrophobic analysis shows that the protein is most probably not directly membrane bound. The second gene, UGX1, has an open reading frame of 573 bp coding for a polypeptide of 191 amino acid residues. The two genes are arranged head to head and share a 192 bp divergent promoter region that contains three TATAAA motives, two for the SNM1 and one for the UGX1 locus. Gene UGX1 has no apparent influence on the sensitivity of the cell to cross-linking nitrogen mustard, as its disruption in wild type does not increase sensitivity to nitrogen mustard and the presence of multiple copies of the gene fails to complement the nitrogen mustard sensitivity phenotype of snm1 disruption mutants. Northern analysis revealed that the expression of SNM1 yields an average of 0.3 copies/cell of a 2.4 kb transcript, while expression of UGX1 yields higher levels of a 0.8 kb poly(A)+ RNA.
一段包含DNA链间交联特异性修复基因SNM1的3.2 kb酵母DNA片段已被测序。鉴定出了两个基因。SNM1有一个1983 bp的开放阅读框,编码一个661个氨基酸的蛋白质。疏水分析表明该蛋白质很可能不直接与膜结合。第二个基因UGX1有一个573 bp的开放阅读框,编码一个由191个氨基酸残基组成的多肽。这两个基因头对头排列,共享一个192 bp的分歧启动子区域,该区域包含三个TATAAA基序,其中两个用于SNM1,一个用于UGX1基因座。基因UGX1对细胞对交联氮芥的敏感性没有明显影响,因为其在野生型中的破坏不会增加对氮芥的敏感性,并且该基因的多个拷贝的存在不能补充snm1破坏突变体的氮芥敏感性表型。Northern分析显示,SNM1的表达产生平均每个细胞0.3拷贝的2.4 kb转录本,而UGX1的表达产生更高水平的0.8 kb poly(A)+ RNA。