Pazin M J, Bhargava P, Geiduschek E P, Kadonaga J T
Department of Biology and Center for Molecular Genetics, University of California, San Diego, La Jolla, CA 92093, USA.
Science. 1997 May 2;276(5313):809-12. doi: 10.1126/science.276.5313.809.
To study nucleosome mobility and positioning, the R3 lac repressor was used with an adenosine triphosphate (ATP)-dependent chromatin assembly system to establish the positioning of five nucleosomes, with one nucleosome located between two R3 lac operators. When R3 protein was dissociated from DNA with isopropyl beta-D-thiogalactopyranoside, the R3-induced nucleosome positions remained unchanged for at least 60 minutes in the absence of ATP but rearranged within 15 minutes in the presence of ATP. These results suggest that nucleosomes are dynamic and mobile rather than static and that a DNA binding factor is continuously required for the maintenance of nucleosome positioning.
为了研究核小体的移动性和定位,R3乳糖阻遏物与一种依赖三磷酸腺苷(ATP)的染色质组装系统一起使用,以确定五个核小体的定位,其中一个核小体位于两个R3乳糖操纵基因之间。当用异丙基β-D-硫代半乳糖苷使R3蛋白与DNA解离时,在没有ATP的情况下,R3诱导的核小体位置至少60分钟保持不变,但在有ATP的情况下15分钟内就会重新排列。这些结果表明,核小体是动态且可移动的,而非静态的,并且维持核小体定位持续需要一种DNA结合因子。