Moran J V, Mecklenburg K L, Sass P, Belcher S M, Mahnke D, Lewin A, Perlman P
Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 75235.
Nucleic Acids Res. 1994 Jun 11;22(11):2057-64. doi: 10.1093/nar/22.11.2057.
Six mutations blocking the function of a seven intron form of the mitochondrial gene encoding subunit I of cytochrome c oxidase (COXI) and mapping upstream of exon 3 were isolated and characterized. A cis-dominant mutant of the group IIA intron 1 defines a helical portion of the C1 substructure of domain 1 as essential for splicing. A trans-recessive mutant confirms that the intron 1 reading frame encodes a maturase function. A cis-dominant mutant in exon 2 was found to have no effect on the splicing of intron 1 or 2. A trans-recessive mutant, located in the group IIA intron 2, demonstrates for the first time that intron 2 encodes a maturase. A genetic dissection of the five missense mutations present in the intron 2 reading frame of that strain demonstrates that the maturase defect results from one or both of the missense mutations in a newly-recognized conserved sequence called domain X.
分离并鉴定了六个突变,这些突变阻断了编码细胞色素c氧化酶亚基I(COXI)的线粒体基因的一种含七个内含子形式的功能,并定位于外显子3上游。IIA组内含子1的一个顺式显性突变体确定结构域1的C1亚结构的一个螺旋部分对于剪接至关重要。一个反式隐性突变体证实内含子1阅读框编码一个成熟酶功能。发现外显子2中的一个顺式显性突变体对内含子1或2的剪接没有影响。位于IIA组内含子2中的一个反式隐性突变体首次证明内含子2编码一个成熟酶。对该菌株内含子2阅读框中存在的五个错义突变进行的遗传分析表明,成熟酶缺陷是由一个新识别的保守序列(称为结构域X)中的一个或两个错义突变导致的。