首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Chromatin fiber folding: requirement for the histone H4 N-terminal tail
Authors:Dorigo Benedetta  Schalch Thomas  Bystricky Kerstin  Richmond Timothy J
Institution:ETH Zürich, Institute for Molecular Biology and Biophysics, ETH-H?nggerberg, CH-8093 Zürich, Switzerland.
Abstract:We have developed a self-assembly system for nucleosome arrays in which recombinant, post-translationally unmodified histone proteins are combined with DNA of defined-sequence to form chromatin higher-order structure. The nucleosome arrays obtained are highly homogeneous and sediment at 53S when maximally folded in 1mM or 100mM MgCl(2). The folding properties are comparable to established systems. Analytical ultracentrifugation is used to determine the consequence of individual histone tail domain deletions on array folding. Fully compacted chromatin fibers are obtained with any one of the histone tails deleted with the exception of the H4 N terminus. The region of the H4 tail, which mediates compaction, resides in the stretch of amino acids 14-19.
Keywords:chromatin fiber  higher-order structure  nucleosome array  histone tails  sedimentation
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号