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酵母线粒体DNA上基因的物理图谱:抗生素抗性位点以及rRNA和tRNA基因的定位

Physical mapping of genes on yeast mitochondrial DNA: localization of antibiotic resistance loci, and rRNA and tRNA genes.

作者信息

Morimoto R, Merten S, Lewin A, Martin N C, Rabinowitz M

出版信息

Mol Gen Genet. 1978 Jul 25;163(3):241-55. doi: 10.1007/BF00271954.

Abstract

We have physically mapped the loci conferring resistance to antibiotics that inhibit mitochondrial protein synthesis (erythromycin, chloramphenicol and paromomycin) or respiration (oligomycin I and II), as well as the 21s and 14s rRNA and tRNA genes on the restriction map of the mitochondrial genome of the yeast Saccharomyces cerevisiae. The mitochondrial genes were localized by hybridization of labeled RNA probes to restriction fragments of grande (strain MH41-7B) mitochondrial DNA (mtDNA) generated by endonucleases EcoRI, HpaI, BamHI, HindIII, SalI, PstI and HhaI. We have derived the HhaI restriction fragment map of MH41-7B mit DNA, to be added to our previously reported maps for the six other endonucleases. The antibiotic resistance loci (antR) were mapped by hybridization of 3H-cRNA transcribed from single marker petite mtDNA's of low kinetic complexity to grande restriction fragments. We have chosen the single Sal I site as the origin of the circular physical map and have positioned the antibiotic loci as follows: C (99.5-1.Ou)--P (27-36.Ou)--OII (58.3-62u--OI (80-84u)--E (94.4-98.4u). The 21s rRNA is localized at 94.4-99.2u, and the 14s rRNA is positioned between 36.2-39.8u. The two rRNA species are separated by 36% of the genome. Total mitochondrial tRNA labeled with 125I hybridized primarily to two regions of the genome, at 99.5-11.5u and 34-44u. A third region of hybridization was occasionally detected at 70--76u, which probably corresponds to seryl and glutamyl tRNA genes, previously located to this region by petite deletion mapping.

摘要

我们已在酿酒酵母线粒体基因组的限制性图谱上,对赋予线粒体蛋白合成抑制剂(红霉素、氯霉素和巴龙霉素)或呼吸抑制剂(寡霉素I和II)抗性的基因座,以及21s和14s rRNA及tRNA基因进行了物理定位。通过将标记的RNA探针与由内切酶EcoRI、HpaI、BamHI、HindIII、SalI、PstI和HhaI产生的酿酒酵母(菌株MH41 - 7B)线粒体DNA(mtDNA)的限制性片段杂交,来定位线粒体基因。我们已得出MH41 - 7B线粒体DNA的HhaI限制性片段图谱,将其添加到我们先前报道的其他六种内切酶的图谱中。通过将低动力学复杂度的单标记小线粒体DNA转录的3H - cRNA与酿酒酵母的限制性片段杂交,来定位抗生素抗性基因座(antR)。我们选择单一的Sal I位点作为环形物理图谱的原点,并将抗生素基因座定位如下:C(99.5 - 1.0u)--P(27 - 36.0u)--OII(58.3 - 62u)--OI(80 - 84u)--E(94.4 - 98.4u)。21s rRNA定位在94.4 - 99.2u,14s rRNA位于36.2 - 39.8u之间。这两种rRNA物种被基因组的36%隔开。用125I标记的总线粒体tRNA主要与基因组的两个区域杂交,分别在99.5 - 11.5u和34 - 44u处。偶尔在70 - 76u处检测到第三个杂交区域,这可能对应于丝氨酰和谷氨酰胺tRNA基因,先前通过小缺失图谱定位到该区域。

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