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酵母线粒体DNA上21S核糖体RNA区域的精细结构。III. 线粒体遗传标记的物理定位及ω的分子性质

Fine structure of the 21S ribosomal RNA region on yeast mitochondrial DNA. III. Physical location of mitochondrial genetic markers and the molecular nature of omega.

作者信息

Heyting C, Menke H H

出版信息

Mol Gen Genet. 1979 Jan 11;168(3):279-91. doi: 10.1007/BF00271498.

Abstract
  1. We have determined the physical location of mitochondrial genetic markers in the 21S region of yeast mtDNA by genetic analysis of petite mutants whose mtDNA has been physically mapped on the wild-type mtDNA. 2. The order of loci, determined in this study, is in agreement with the order deduced from recombination analysis and coretention analysis except for the position of omega+: we conclude that omega+ is located between C321 (RIB-1) and E514 (RIB-3). 3. The marker E514 (RIB-3) has been localized on a DNA segment of 3800 bp, and the markers E354, E553 and cs23 (RIB-2) on a DNA segment of 1100 base pairs; both these segments overlap the 21S rRNA cistron. The marker C321 (RIB-1) has been localized within a segment of 240 bp which also overlaps the 21S rRNA cistron, and we infer on the basis of indirect evidence that this marker lies within this cistron. 4. In all our rho+ as well as rho- strains there is a one-to-one correlation between the omega+ phenotype, the ability to transmit the omega+ allele and the presence of a mtDNA segment of about 1000 bp long, located between sequences specifying RIB-3 and sequences corresponding to the loci RIB-1 and RIB-2. This segment may be inserted at this same position into omega- mtDNA by recombination. 5. The role which the different allelic forms of omega may play in the polarity of recombination is discussed.
摘要
  1. 通过对小菌落突变体进行遗传分析,我们确定了酵母线粒体DNA(mtDNA)21S区域中线粒体遗传标记的物理位置,这些小菌落突变体的mtDNA已在野生型mtDNA上进行了物理定位。2. 本研究确定的基因座顺序与通过重组分析和共保留分析推导的顺序一致,但ω+的位置除外:我们得出结论,ω+位于C321(RIB-1)和E514(RIB-3)之间。3. 标记E514(RIB-3)已定位在一段3800 bp的DNA片段上,标记E354、E553和cs23(RIB-2)定位在一段1100个碱基对的DNA片段上;这两个片段都与21S rRNA顺反子重叠。标记C321(RIB-1)已定位在一段240 bp的片段内,该片段也与21S rRNA顺反子重叠,并且我们根据间接证据推断该标记位于这个顺反子内。4. 在我们所有的ρ+和ρ-菌株中,ω+表型、传递ω+等位基因的能力与位于指定RIB-3的序列和对应于RIB-1和RIB-2基因座的序列之间的一段约1000 bp长的mtDNA片段的存在之间存在一对一的相关性。该片段可通过重组插入到ω- mtDNA的相同位置。5. 讨论了ω的不同等位基因形式在重组极性中可能发挥的作用。

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