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Identification of differentially expressed genes in yeast Saccharomyces cerevisiae cells with inactivated Mmf1p and Hmf1p, members of proteins family YERO57c/YJGF

机译:酵母酿酒酵母细胞中失活的Mmf1p和Hmf1p(YERO57c / YJGF蛋白家族成员)的差异表达基因的鉴定

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摘要

We used differential display analysis of mRNA to investigate the differences between gene expression in wild-type (wt) yeast Saccharomyces cerevisiae cells and mutated ones with disrupted activity of genes MMF1 and HMF1, members of the YERO57c/YJGF family. Reverse transcription-polymerase chain reaction (RT-PCR) analysis was performed to determine the differences in the degree of expression of 14 specific transcripts in normal and mutated yeast cells. Obtained data demonstrate that disruption of genes encoding proteins Mmf1p, Hmf1p (or both of them) result in the correlative variation of expression level of the target 12 genes both in the cells with changed phenotype (mmf1 and mmf1 hmf1) and in the cells retaining w.t. shape and growth rate (wt cells, hmf1). Metabolic processes and cellular pathways have been indicated for Mmf1p and Hmf1p based on the different profiles of the expression of 14 genes in mmf1, hmf1 yeast S. cerevisiae cells.
机译:我们使用mRNA的差异显示分析来研究野生型(wt)酿酒酵母细胞中的基因表达与YERO57c / YJGF家族成员MMF1和HMF1基因活性被破坏的突变细胞之间的基因表达差异。进行了逆转录聚合酶链反应(RT-PCR)分析,以确定正常和突变酵母细胞中14种特定转录本的表达程度差异。获得的数据表明,编码蛋白Mmf1p,Hmf1p(或它们两者)的基因的破坏导致表型(mmf1和mmf1 hmf1)改变的细胞以及保留w.t.的细胞中靶12基因表达水平的相关变化。形状和生长速率(wt细胞,hmf1)。基于mmf1,hmf1酵母酿酒酵母细胞中14个基因表达的不同情况,已表明Mmf1p和Hmf1p的代谢过程和细胞途径。

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