Vogelauer M, Cioci F, Camilloni G
Dípartimento di Genetica e Biologia Molecolare, Università di Roma, La Sapienza, Rome, Italy.
J Mol Biol. 1998 Jan 16;275(2):197-209. doi: 10.1006/jmbi.1997.1451.
This study represents a detailed analysis of the structural context of the RNA polymerase I promoter of Saccharomyces cerevisiae. We determined the presence of regularly spaced nucleosomes in the non-transcribed spacer (NTS) and found that five of them have well defined positions. We show that this nucleosome positioning is restricted to the region between the 35 S and 5 S rRNA promoters, beyond which a more delocalized chromatin structure is evident. A more refined analysis detects the DNA-protein interactions on the RNA polymerase I promoter at nucleotide resolution and provides the first in vivo footprints, attributable to factors like REB1, CF, UAF and an additional protection that seems to be sensitive to the topological context. Moreover, when this analysis is extended to different growth media (YPD versus YNB), some of these protections show a growth condition dependent behaviour.
本研究对酿酒酵母RNA聚合酶I启动子的结构背景进行了详细分析。我们确定了非转录间隔区(NTS)中存在规则间隔的核小体,并发现其中五个核小体具有明确的位置。我们表明,这种核小体定位仅限于35S和5S rRNA启动子之间的区域,在此区域之外,更弥散的染色质结构很明显。更精细的分析以核苷酸分辨率检测RNA聚合酶I启动子上的DNA-蛋白质相互作用,并提供了首个体内足迹,这些足迹归因于REB1、CF、UAF等因子以及一种似乎对拓扑背景敏感的额外保护。此外,当将此分析扩展到不同的生长培养基(YPD与YNB)时,其中一些保护表现出依赖生长条件的行为。