Woontner M, Jaehning J A
Department of Biology, Indiana University, Bloomington 47405.
Yeast. 1993 Dec;9(12):1331-4. doi: 10.1002/yea.320091206.
We demonstrate the successful adaptation to other yeast species of a protocol previously described for production of transcriptionally active whole cell extracts from Saccharomyces cerevisiae (Woontner and Jaehning, 1990, J. Biol. Chem. 265, 8979-8982). Extracts prepared from Schizosaccharomyces pombe, Kluyveromyces lactis and Candida glabrata were all capable of initiating transcription from a template containing the S. cerevisiae CYC1 TATA box fused to a G-less cassette. Transcription in all of the extracts was sensitive to inhibition by alpha-amanitin, indicating that it was catalysed by RNA polymerase II, and was dramatically stimulated by the chimeric activator GAL4/VP16. The different extracts used different subsets of a group of three initiation sites.
我们证明了一种先前描述的用于从酿酒酵母中制备转录活性全细胞提取物的方案(Woontner和Jaehning,1990年,《生物化学杂志》265卷,8979 - 8982页)能够成功适用于其他酵母物种。从粟酒裂殖酵母、乳酸克鲁维酵母和光滑念珠菌制备的提取物均能够从含有与无鸟苷盒融合的酿酒酵母CYC1 TATA框的模板起始转录。所有提取物中的转录均对α-鹅膏蕈碱抑制敏感,表明其由RNA聚合酶II催化,并且受到嵌合激活剂GAL4/VP16的显著刺激。不同的提取物使用了一组三个起始位点中的不同子集。