Nham S U, Wilkemeyer M F, Ledley F D
Howard Hughes Medical Institute, Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030.
Genomics. 1990 Dec;8(4):710-6. doi: 10.1016/0888-7543(90)90259-w.
The MUT locus encoding the enzyme methylmalonyl-CoA mutase is defective in mut forms of methylmalonic acidemia. This locus has been mapped to chromosome 6p12-21.1. We report cloning and characterization of this locus which comprises 13 exons spanning greater than 35 kb of the genome. The MUT locus exhibits consensus sequences for transcription, splicing, and polyadenylation. The putative promoter region was localized in a CG island 5' to exon I and was shown to direct expression of a beta-galactosidase reporter gene in cultured cells. Of interest is the observation that the first intron occurs within the 5' untranslated region, and no introns separate the mitochondrial targeting sequences and the mature apoenzyme. An informative HindIII polymorphism was localized within the coding sequence and can be assayed using the polymerase chain reaction. These studies describe the structure of the MUTlocus and provide a foundation for characterization of mutations in mut methylmalonic acidemia.
编码甲基丙二酰辅酶A变位酶的MUT基因座在甲基丙二酸血症的mut型中存在缺陷。该基因座已被定位到6号染色体的p12 - 21.1区域。我们报告了该基因座的克隆和特征分析,它由13个外显子组成,跨越基因组超过35 kb。MUT基因座具有转录、剪接和聚腺苷酸化的共有序列。推测的启动子区域位于外显子I 5'端的一个CG岛中,并在培养细胞中显示出指导β - 半乳糖苷酶报告基因的表达。有趣的是,观察到第一个内含子出现在5'非翻译区内,并且没有内含子分隔线粒体靶向序列和成熟的脱辅基酶。一个信息丰富的HindIII多态性位于编码序列内,可以使用聚合酶链反应进行检测。这些研究描述了MUT基因座的结构,并为mut型甲基丙二酸血症中突变的特征分析提供了基础。