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酵母线粒体基因组的物理图谱:D273 - 10B菌株精细结构和基因图谱的推导以及与基因组大小不同的菌株(MH41 - 7B)的比较。

Physical mapping of the yeast mitochondrial genome: derivation of the fine structure and gene map of strain D273-10B and comparison with a strain (MH41-7B) differing in genome size.

作者信息

Morimoto R, Rabinowitz M

出版信息

Mol Gen Genet. 1979 Feb 16;170(1):25-48.

PMID:375015
Abstract

(1) We have derived a fine-structure map of the 70 kb mitochondrial genome of the yeast S. cerevisiae, strain D273-10B, and compared it with our previous maps for strain MH41-7B. Restriction fragment maps for 56 enzyme recognition sites for 13 endonucleases, Eco RI, Hpa I, Bam HI, Hha I, Hinc II, Xba I, Hind III, Bgl II, Pvu II, Sal I, Pst I, Sst I, and Xho I, have been derived. We have used several methods to obtain these maps: (a) Four enzymes (Sal I, Sst I, Xho I, Pst I), each of which cuts D273-10B mtDNA at a single site, were employed to localize and orient fragments from multi-site enzyme digests that are cleaved by the single-site enzyme. (b) Radioactively labeled probes (rRNA or copy RNA [cRNA] transcribed from simple-sequence petite mtDNA) were hybridized to restriction fragments from different digests for identification of fragments which share common sequences. (c) The products of double or triple enzyme digests were identified for mapping and confirmation of the localization of restriction sites. (2) The antibiotic-resistant (antR) loci for erythromycin (E), chloramphenicol (C), paromomycin (P), and oligomycin (OI, OII) were positioned on the physical restriction map by hybridization of 3H-labeled cRNA transcribed from simple-sequence petite mtDNAs that retain a single genetic antR marker to appropriate restriction fragments bound to nitrocellulose filters. (3) Mitochondrial transcripts (21s rRNA, 14s rRNA, and tRNAs) labeled with 125I were hybridized to restriction fragments for identification of the corresponding coding sequence. (4) The gene order and localization of the antR loci and mitochondrial transcripts are as follows: C(0-1.5u)-tRNA I(0-21.5u)-P(29-36.6u)-tRNA II(29-46.4u)-14s rRNA(36-38.3u)-OII(60.3-62.5u) - tRNA III(73-76u) - OI(78.6-83.0u) - tRNA IV(82.5-83.0u) - E(94.2-98.6u) - 21s rRNA (94.2-99.4u). (5) The DNA fine structure and gene map of the 70 kb D273-10B mtDNA were compared to the map of the larger MH41-7B (76 kb) mtDNA. There are 56 restriction sites on D273-10B and 67 sites on MH41-7B for the 13 enzymes studied. The additional restriction sites are largely accounted for by the presence, in MH41-7B, of two sets of sequences, "A" (2.7 kb) and "B" (3.0 kb), located on either side of the OII marker. The remainder of the fragments map is remarkably similar for the two strains. The distances separating the antR loci and the mitochondrial transcripts are very similar except in the two regions surrounding OII.

摘要

(1) 我们绘制了酿酒酵母D273 - 10B菌株70 kb线粒体基因组的精细结构图,并将其与我们之前绘制的MH41 - 7B菌株的图谱进行了比较。已得出针对13种核酸内切酶(Eco RI、Hpa I、Bam HI、Hha I、Hinc II、Xba I、Hind III、Bgl II、Pvu II、Sal I、Pst I、Sst I和Xho I)的56个酶识别位点的限制性片段图谱。我们使用了几种方法来获取这些图谱:(a) 四种酶(Sal I、Sst I、Xho I、Pst I),每种酶在D273 - 10B线粒体DNA上仅切割一个位点,用于定位和定向来自多位点酶切的片段,这些片段可被单一位点酶切割。(b) 将放射性标记的探针(从简单序列小菌落线粒体DNA转录而来的rRNA或拷贝RNA [cRNA])与来自不同酶切的限制性片段杂交,以鉴定具有共同序列的片段。(c) 鉴定双酶切或三酶切产物,用于图谱绘制和限制酶切位点定位的确认。(2) 通过将从保留单个遗传抗药标记的简单序列小菌落线粒体DNA转录而来的3H标记cRNA与结合在硝酸纤维素滤膜上的适当限制性片段杂交,将红霉素(E)、氯霉素(C)、巴龙霉素(P)和寡霉素(OI、OII)的抗生素抗性(antR)位点定位在物理限制性图谱上。(3) 用125I标记的线粒体转录本(21s rRNA、14s rRNA和tRNAs)与限制性片段杂交,以鉴定相应的编码序列。(4) 抗药位点和线粒体转录本的基因顺序及定位如下:C(0 - 1.5u) - tRNA I(0 - 21.5u) - P(29 - 36.6u) - tRNA II(29 - 46.4u) - 14s rRNA(36 - 38.3u) - OII(60.3 - 62.5u) - tRNA III(73 - 76u) - OI(78.6 - 83.0u) - tRNA IV(82.5 - 83.0u) - E(94.2 - 98.6u) - 21s rRNA (94.2 - 99.4u)。(5) 将70 kb D273 - 10B线粒体DNA的DNA精细结构和基因图谱与更大的MH41 - (76 kb)线粒体DNA的图谱进行了比较。在所研究的13种酶中,D273 - 10B上有56个限制性位点,MH41 - 7B上有67个位点。额外的限制性位点主要是由于在MH41 - 7B中,位于OII标记两侧存在两组序列,“A”(2.7 kb)和“B”(3.0 kb)。对于这两个菌株,其余片段图谱非常相似。除了围绕OII的两个区域外,抗药位点和线粒体转录本之间的距离非常相似。

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