Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States.
Acc Chem Res. 2021 Aug 17;54(16):3215-3227. doi: 10.1021/acs.accounts.1c00313. Epub 2021 Jul 28.
The fundamental repeating unit of chromatin, the nucleosome, is composed of DNA wrapped around two copies each of four canonical histone proteins. Nucleosomes possess 2-fold pseudo-symmetry that is subject to disruption in cellular contexts. For example, the post-translational modification (PTM) of histones plays an essential role in epigenetic regulation, and the introduction of a PTM on only one of the two "sister" histone copies in a given nucleosome eliminates the inherent symmetry of the complex. Similarly, the removal or swapping of histones for variants or the introduction of a histone mutant may render the two faces of the nucleosome asymmetric, creating, if you will, a type of "Janus" bioparticle. Over the past decade, many groups have detailed the discovery of asymmetric species in chromatin isolated from numerous cell types. However, in vitro biochemical and biophysical investigation of asymmetric nucleosomes has proven synthetically challenging. Whereas symmetric nucleosomes are readily formed via a stochastic combination of their histone and DNA components, asymmetric nucleosome assembly demands the selective incorporation of a single modified/mutant histone copy alongside its wild-type counterpart.Herein we describe the chemical biology tools that we and others have developed in recent years for investigating nucleosome asymmetry. Such approaches, each with its own benefits and shortcomings, fall into five broad categories. First, we discuss affinity tag-based purification methods. These enable the assembly of theoretically any asymmetric nucleosome of interest but are frequently labor-intensive and suffer from low yields. Second, we detail transient cross-linking strategies that are amenable to the preparation of histone H3- or H4-modified/mutant asymmetric species. These yield asymmetric nucleosomes in a traceless fashion, albeit through the use of more complicated synthesis techniques. Third, we describe a synthetic biology technique based on the generation of bump-hole mutant H3 histones that selectively heterodimerize. Although currently developed only for H3 and a related isoform, this method uniquely allows for the interrogation of nucleosome asymmetry in yeast. Fourth, we outline a method for generating H2A- or H2B-modified/mutant asymmetric nucleosomes that relies on the differential DNA-histone contact strength inherent in the Widom 601 DNA sequence. This technique involves the initial formation of hexasomes which are then complemented with distinct H2A/H2B dimers. Finally, we review an approach that utilizes split intein technology to isolate asymmetric H2A- or H2B-modified/mutant nucleosomes. This method shares steps in common with the former but exploits tagged, intein-fused dimers for the facile purification of asymmetric products.Throughout the Account, we highlight various biological questions that drove the development of these methods and ultimately were answered by them. Though each technique has its own shortcomings, collectively these chemical biology tools provide a means to biochemically interrogate a plethora of asymmetric nucleosome species. We conclude with a discussion of remaining challenges, particularly that of endogenous asymmetric nucleosome detection.
染色质的基本重复单元核小体由两条各含两个拷贝的组蛋白组成。核小体具有 2 重拟态对称性,这种对称性在细胞环境中会被破坏。例如,组蛋白的翻译后修饰(PTM)在表观遗传调控中起着至关重要的作用,在给定核小体中两个“姐妹”组蛋白拷贝之一上引入 PTM 会消除复合物的固有对称性。同样,组蛋白变体的替换或组蛋白突变体的引入可能使核小体的两面不对称,从而创造出一种“两面神”生物粒子。在过去的十年中,许多研究小组详细描述了从许多细胞类型中分离出的染色质中不对称物种的发现。然而,体外生化和生物物理研究表明,不对称核小体的合成具有挑战性。虽然对称核小体可以通过其组蛋白和 DNA 成分的随机组合轻易形成,但不对称核小体的组装需要选择性地掺入单个修饰/突变组蛋白拷贝及其野生型对应物。本文描述了我们和其他研究小组近年来开发的用于研究核小体不对称性的化学生物学工具。这些方法各有优缺点,大致可分为五类。首先,我们讨论了基于亲和标签的纯化方法。这些方法可用于组装任何理论上感兴趣的不对称核小体,但通常劳动强度大,产量低。其次,我们详细介绍了适用于制备组蛋白 H3 或 H4 修饰/突变不对称物种的瞬时交联策略。这些方法以无痕迹的方式产生不对称核小体,但需要更复杂的合成技术。第三,我们描述了一种基于产生选择性异二聚化的 bump-hole 突变体 H3 组蛋白的合成生物学技术。尽管目前仅开发用于 H3 和相关同工型,但该方法独特地允许在酵母中研究核小体的不对称性。第四,我们概述了一种生成 H2A 或 H2B 修饰/突变不对称核小体的方法,该方法依赖于 Widom 601 DNA 序列中固有的 DNA-组蛋白接触强度差异。该技术涉及六聚体的初始形成,然后用不同的 H2A/H2B 二聚体进行补充。最后,我们回顾了一种利用分裂整合酶技术分离不对称 H2A 或 H2B 修饰/突变核小体的方法。该方法与前一种方法有共同之处,但利用标记的、融合了整合酶的二聚体来方便地纯化不对称产物。在整个叙述中,我们强调了推动这些方法发展的各种生物学问题,并最终通过这些方法得到了回答。虽然每种技术都有其自身的缺点,但这些化学生物学工具共同为研究大量不对称核小体物种提供了一种生物化学手段。我们最后讨论了剩余的挑战,特别是内源性不对称核小体检测的挑战。