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梨形四膜虫ST株线粒体DNA中核糖体RNA基因的组织方式。

The organization of ribosomal RNA genes in the mitochondrial DNA of Tetrahymena pyriformis strain ST.

作者信息

Goldbach R W, Borst P, Bollen-de Boer J E, van Bruggen E F

出版信息

Biochim Biophys Acta. 1978 Nov 21;521(1):169-86. doi: 10.1016/0005-2787(78)90260-5.

Abstract
  1. We have constructed a physical map of the mtDNA of Tetrahymena pyriformis strain ST using the restriction endonucleases EcoRI, PstI, SacI, HindIII and HhaI. 2. Hybridization of mitochondrial 21 S and 14 S ribosomal RNA to restriction fragments of strain ST mtDNA shows that this DNA contains two 21-S and only one 14-S ribosomal RNA genes. By S1 nuclease treatment of briefly renatured single-stranded DNA the terminal duplication-inversion previously detected in this DNA (Arnberg et al. (1975) Biochim. Biophys. Acta 383, 359--369) has been isolated and shown to contain both 21-S ribosomal RNA genes. 14 S ribosomal RNA hybridizes to a region in the central part of the DNA, about 8000 nucleotides or 20% of the total DNA length apart from the nearest 21 S ribosomal RNA gene. 3. We have confirmed this position of the three ribosomal RNA genes by electron microscopical analysis of DNA . RNA hybrid molecules and R-loop molecules. 4. Hybridization of 21 S ribosomal RNA with duplex mtDNA digested either with phage lambda-induced exonuclease or exonuclease III of Escherichia coli, shows that the 21-S ribosomal RNA genes are located on the 5'-ends of each DNA strand. Electron microscopy of denaturated mtDNA hybridized with a mixture of 14-S and 21-S ribosomal RNAs show that the 14 S ribosomal RNA gene has the same polarity as the nearest 21 S ribosomal RNA gene. 5. Tetrahymena mtDNA is (after Saccharomyces mtDNA) the second mtDNA in which the two ribosomal RNA cistrons are far apart and the first mtDNA in which one of the ribosomal RNA cistrons is duplicated.
摘要
  1. 我们使用限制性内切酶EcoRI、PstI、SacI、HindIII和HhaI构建了梨形四膜虫ST株系线粒体DNA(mtDNA)的物理图谱。2. 线粒体21S和14S核糖体RNA与ST株系mtDNA的限制性片段杂交表明,该DNA包含两个21S核糖体RNA基因和仅一个14S核糖体RNA基因。通过对短暂复性的单链DNA进行S1核酸酶处理,先前在该DNA中检测到的末端重复-倒位(Arnberg等人,(1975年)《生物化学与生物物理学报》383卷,359 - 369页)已被分离出来,并显示其包含两个21S核糖体RNA基因。14S核糖体RNA与DNA中部的一个区域杂交,该区域距离最近的21S核糖体RNA基因约8000个核苷酸或占总DNA长度的20%。3. 我们通过对DNA - RNA杂交分子和R环分子的电子显微镜分析,证实了这三个核糖体RNA基因的位置。4. 用噬菌体λ诱导的核酸外切酶或大肠杆菌核酸外切酶III消化的双链mtDNA与21S核糖体RNA杂交表明,21S核糖体RNA基因位于每条DNA链的5'端。用14S和21S核糖体RNA混合物杂交的变性mtDNA的电子显微镜观察表明,14S核糖体RNA基因与最近的21S核糖体RNA基因具有相同的极性。5. 四膜虫mtDNA是(仅次于酿酒酵母mtDNA)第二个两个核糖体RNA顺反子相距很远的mtDNA,也是第一个其中一个核糖体RNA顺反子被复制的mtDNA。

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