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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Morawiec, E.a , Wichtowska, D.a , Graczyk, D.a f , Conesa, C.b c d , Lefebvre, O.b c d , Boguta, M.a e Maf1, repressor of tRNA transcription, is involved in the control of gluconeogenetic genes in Saccharomyces cerevisiae
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Morawiec, E.a , Wichtowska, D.a , Graczyk, D.a f , Conesa, C.b c d , Lefebvre, O.b c d , Boguta, M.a e Maf1, repressor of tRNA transcription, is involved in the control of gluconeogenetic genes in Saccharomyces cerevisiae

机译:Morawiec,E.a,Wichtowska,D.a,Graczyk,D.af,Conesa,C.b c d,Lefebvre,O.b c d,Boguta,M.a e Maf1,tRNA转录阻遏物,参与酿酒酵母糖原异生基因的控制。

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摘要

Maf1 is a negative regulator of RNA polymerase III (Pol III) in yeast. Maf1-depleted cells manifest elevated tRNA transcription and inability to grow on non-fermentable carbon source, such as glycerol. Using genomic microarray approach, we examined the effect of Maf1 deletion on expression of Pol II-transcribed genes in yeast grown in medium containing glycerol. We found that transcription of FBP1 and PCK1, two major genes controlling gluconeogenesis, was decreased in maf1δ cells. FBP1 is located on chromosome XII in close proximity to a tRNA-Lys gene. Accordingly we hypothesized that decreased FBP1 mRNA level could be due to the effect of Maf1 on tgm silencing (tRNA gene mediated silencing). Two approaches were used to verify this hypothesis. First, we inactivated tRNA-Lys gene on chromosome XII by inserting a deletion cassette in a control wild type strain and in maf1δ mutant. Second, we introduced a point mutation in the promoter of the tRNA-Lys gene cloned with the adjacent FBP1 in a plasmid and expressed in fbp1δ or fbp1δ maf1δ cells. The levels of FBP1 mRNA were determined by RT-qPCR in each strain. Although the inactivation of the chromosomal tRNA-Lys gene increased expression of the neighboring FBP1, the mutation preventing transcription of the plasmid-born tRNA-Lys gene had no significant effect on FBP1 transcription. Taken together, those results do not support the concept of tgm silencing of FBP1. Other possible mechanisms are discussed.
机译:Maf1是酵母中RNA聚合酶III(Pol III)的负调节剂。缺乏Maf1的细胞表现出升高的tRNA转录,并且无法在不可发酵的碳源(如甘油)上生长。使用基因组微阵列方法,我们检查了Maf1缺失对在含甘油培养基中生长的酵母中Pol II转录基因表达的影响。我们发现在maf1δ细胞中,控制糖异生的两个主要基因FBP1和PCK1的转录降低了。 FBP1位于XII染色体上,紧邻tRNA-Lys基因。因此,我们假设FBP1 mRNA水平降低可能是由于Maf1对tgm沉默(tRNA基因介导的沉默)的影响。使用两种方法来验证该假设。首先,我们通过在控制野生型菌株和maf1δ突变体中插入缺失盒使XII染色体上的tRNA-Lys基因失活。其次,我们在与质粒中的相邻FBP1克隆并在fbp1δ或fbp1δmaf1δ细胞中表达的tRNA-Lys基因的启动子中引入了点突变。通过RT-qPCR确定每个菌株中的FBP1mRNA水平。尽管染色体tRNA-Lys基因的失活增加了邻近FBP1的表达,但阻止质粒出生的tRNA-Lys基因转录的突变对FBP1转录没有显着影响。综上所述,这些结果不支持FBP1的tgm沉默的概念。讨论了其他可能的机制。

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