Rondón Ana G, García-Rubio María, González-Barrera Sergio, Aguilera Andrés
Departamento de Genética, Facultad de Biología, Universidad de Sevilla, Avd. Reina Mercedes 6, E-41012 Sevilla, Spain.
EMBO J. 2003 Feb 3;22(3):612-20. doi: 10.1093/emboj/cdg047.
We have previously shown that yeast mutants of the THO complex have a defect in gene expression, observed as an impairment of lacZ transcription. Here we analyze the ability of mutants of different transcription elongation factors to transcribe lacZ. We found that spt4Delta, like THO mutants, impaired transcription of lacZ and of long and GC-rich DNA sequences fused to the GAL1 promoter. Using a newly developed in vitro transcription elongation assay, we show that Spt4 is required in elongation. There is a functional interaction between Spt4 and THO, detected by the lethality or strong gene expression defect and hyper-recombination phenotypes of double mutants in the W303 genetic background. Our results indicate that Spt4-Spt5 has a positive role in transcription elongation and suggest that Spt4-Spt5 and THO act at different steps during mRNA biogenesis.
我们之前已经表明,THO复合物的酵母突变体在基因表达方面存在缺陷,表现为lacZ转录受损。在此,我们分析了不同转录延伸因子的突变体转录lacZ的能力。我们发现,与THO突变体一样,spt4Δ会损害lacZ以及与GAL1启动子融合的长且富含GC的DNA序列的转录。使用新开发的体外转录延伸测定法,我们表明延伸过程中需要Spt4。在W303遗传背景下,通过双突变体的致死性或强烈的基因表达缺陷以及高重组表型检测到Spt4与THO之间存在功能相互作用。我们的结果表明,Spt4-Spt5在转录延伸中具有积极作用,并表明Spt4-Spt5和THO在mRNA生物合成过程中的不同步骤发挥作用。