核小体
生物
基因组
染色质
计算生物学
进化生物学
折叠(DSP实现)
遗传学
DNA
基因
电气工程
工程类
作者
Abrar Aljahani,Clemens Mauksch,A. Marieke Oudelaar
标识
DOI:10.1016/j.ceb.2024.102398
摘要
Eukaryotic genomes are organized into 3D structures, which range from small-scale nucleosome arrays to large-scale chromatin domains. These structures have an important role in the regulation of transcription and other nuclear processes. Despite advances in our understanding of the properties, functions, and underlying mechanisms of genome structures, there are many open questions about the interplay between these structures across scales. In particular, it is not well understood if and how 1D features of nucleosome arrays influence large-scale 3D genome folding patterns. In this review, we discuss recent studies that address these questions and summarize our current understanding of the relationship between nucleosome positioning and higher-order genome folding.
科研通智能强力驱动
Strongly Powered by AbleSci AI