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对酿酒酵母十二号染色体左臂上六个新开放阅读框的功能分析表明,其中三个对硫饥饿有反应。

Functional Analysis of six novel ORFs on the left arm of Chromosome XII of Saccharomyces cerevisiae reveals three of them responding to S-starvation.

作者信息

Zhang N, Merlotti C, Wu J, Ismail T, El-Moghazy A N, Khan S A, Butt A, Gardner D C, Sims P F, Oliver S G

机构信息

School of Biological Sciences, University of Manchester, Oxford Road, Manchester M13 9PT, UK.

出版信息

Yeast. 2001 Mar 15;18(4):325-34. doi: 10.1002/1097-0061(20010315)18:4<325::AID-YEA669>3.0.CO;2-K.

Abstract

Six novel Open Reading Frames (ORFs) located on the left arm of the chromosome XII (YLL061w, YLL060c, YLL059c, YLL058w, YLL057c and YLL056c) have been analysed using either short-flanking homology (SFH) or long-flanking homology (LFH) gene replacement. Sporulation and tetrad analysis showed none of these ORFs to be essential for vegetative growth. The standard EUROFAN growth tests failed to reveal any obvious phenotypes resulting from deletion of each of the ORFs. Bioinformatic analysis revealed that YLL061w is probably an amino acid permease for S-methylmethionine and that YLL060c encodes a glutathione transferase which is involved in cellular detoxification, while YLL058w may play a role in sulphur-containing amino-acid metabolism, YLL057c in sulphonate catabolism and YLL056c in stress response. The transcription of three ORFs (YLL061w, YLL057c and YLL056c) has been shown to increase more than 10-fold under sulphate starvation. Replacement cassettes, comprising the kanMX marker flanked by each ORF's promoter and terminator regions, were cloned into pUG7. All the cognate clones, were generated using direct PCR products amplified from genomic DNA or using gap-repair. All clones and strains produced have been deposited in the EUROFAN genetic stock centre (EUROSCARF, Frankfurt).

摘要

位于第十二号染色体左臂上的六个新开放阅读框(ORF)(YLL061w、YLL060c、YLL059c、YLL058w、YLL057c和YLL056c)已通过短侧翼同源性(SFH)或长侧翼同源性(LFH)基因替换进行了分析。孢子形成和四分体分析表明,这些ORF对营养生长均非必需。标准的EUROFAN生长测试未能揭示因每个ORF缺失而产生的任何明显表型。生物信息学分析表明,YLL061w可能是S-甲基甲硫氨酸的氨基酸通透酶,YLL060c编码一种参与细胞解毒的谷胱甘肽转移酶,而YLL058w可能在含硫氨基酸代谢中起作用,YLL057c在磺酸盐分解代谢中起作用,YLL056c在应激反应中起作用。已证明三个ORF(YLL061w、YLL057c和YLL056c)的转录在硫酸盐饥饿条件下增加了10倍以上。包含由每个ORF的启动子和终止子区域侧翼的kanMX标记的替换盒被克隆到pUG7中。所有同源克隆均使用从基因组DNA扩增的直接PCR产物或使用缺口修复产生。所有产生的克隆和菌株均已保存在EUROFAN遗传储备中心(EUROSCARF,法兰克福)。

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