首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Molecular analysis of Saccharomyces cerevisiae chromosome I: identification of additional transcribed regions and demonstration that some encode essential functions.
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Molecular analysis of Saccharomyces cerevisiae chromosome I: identification of additional transcribed regions and demonstration that some encode essential functions.

机译:酿酒酵母染色体I的分子分析:识别其他转录区域并证明其中一些编码基本功能。

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Saccharomyces cerevisiae chromosome I has provided a vivid example of the "gene-number paradox." Although molecular studies have suggested that there are greater than 100 transcribed regions on the chromosome, classical genetic studies have identified only about 15 genes, including just 6 identified in intensive studies using Ts- lethal mutations. To help elucidate the reasons for this disparity, we have undertaken a detailed molecular analysis of a 34-kb segment of the left arm of the chromosome. This segment contains the four known genes CDC24, WHI1, CYC3 and PYK1 plus at least seven transcribed regions of unknown function. The 11 identified transcripts have a total length of approximately 25.9 kb, suggesting that greater than or equal to 75% of the DNA in this region is transcribed. Of the transcribed regions of unknown function, three are essential for viability on rich medium and three appear to be nonessential, as judged by the lethality or nonlethality of deletions constructed using integrative transformation methods. No obvious phenotypes were associated with the deletions in the apparently nonessential genes. However, two of these genes may have homologs elsewhere in the genome, as judged from the appearance of additional bands when DNA-DNA blot hybridizations were performed at reduced stringency. Taken together, the results provide further evidence that the limitations of classical genetic studies of chromosome I cannot be explained solely by a lack of genes, or even a lack of essential genes, on the chromosome.
机译:酿酒酵母I染色体提供了“基因数悖论”的生动例子。尽管分子研究表明,染色体上有100个以上的转录区域,但经典的遗传研究仅鉴定了约15个基因,其中只有6个在使用Ts致死突变的强化研究中鉴定。为了帮助阐明这种差异的原因,我们对染色体左臂的34kb片段进行了详细的分子分析。该区段包含四个已知基因CDC24,WHI1,CYC3和PYK1,以及至少七个功能未知的转录区。鉴定出的11个转录本的总长度约为25.9 kb,表明该区域中转录的DNA大于或等于75%。在功能未知的转录区域中,三个区域对于在丰富培养基上的生存力至关重要,而三个区域则显得无关紧要,这可以通过使用整合转化方法构建的缺失的致死性或非致死性来判断。没有明显的表型与显然非必需基因的缺失无关。然而,当以降低的严格性进行DNA-DNA印迹杂交时,从另外的条带的出现判断,这些基因中的两个可能在基因组中的其他地方具有同源物。综上所述,结果提供了进一步的证据,即不能仅通过染色体上缺乏基因,甚至缺乏必需基因来解释I号染色体经典遗传研究的局限性。

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