Schultz M C, Choe S Y, Reeder R H
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Proc Natl Acad Sci U S A. 1991 Feb 1;88(3):1004-8. doi: 10.1073/pnas.88.3.1004.
A protocol is described for making a soluble whole-cell extract from yeast (Saccharomyces cerevisiae) that supports active and specific transcription initiation by RNA polymerases I, II, and III. Specific initiation by polymerase I decreases in high-density cultures, paralleling the decrease in abundance of the endogenous 35S rRNA precursor. This extract should be useful for studying the molecular mechanisms that regulate rRNA transcription in yeast.
本文描述了一种从酵母(酿酒酵母)中制备可溶性全细胞提取物的方法,该提取物可支持RNA聚合酶I、II和III进行活性和特异性转录起始。在高密度培养中,聚合酶I的特异性起始作用会降低,这与内源性35S rRNA前体丰度的降低相平行。这种提取物对于研究酵母中调节rRNA转录的分子机制应该是有用的。