Leiden Institute of Chemistry, Leiden University, Leiden, The Netherlands.
Centre for Microbial Cell Biology, Leiden University, Leiden, The Netherlands.
Nat Commun. 2024 Sep 11;15(1):7950. doi: 10.1038/s41467-024-52337-y.
Histones are important chromatin-organizing proteins in eukaryotes and archaea. They form superhelical structures around which DNA is wrapped. Recent studies have shown that some archaea and bacteria contain alternative histones that exhibit different DNA binding properties, in addition to highly divergent sequences. However, the vast majority of these histones are identified in metagenomes and thus are difficult to study in vivo. The recent revolutionary breakthroughs in computational protein structure prediction by AlphaFold2 and RoseTTAfold allow for unprecedented insights into the potential function and structure of previously uncharacterized proteins. Here, we categorize the prokaryotic histone space into 17 distinct groups based on AlphaFold2 predictions. We identify a superfamily of histones, termed α3 histones, which are common in archaea and present in several bacteria. Importantly, we establish the existence of a large family of histones throughout archaea and in some bacteriophages that, instead of wrapping DNA, bridge DNA, thereby diverging from conventional nucleosomal histones.
组蛋白是真核生物和古菌中重要的染色质组织蛋白。它们形成超螺旋结构,DNA 缠绕在这些结构周围。最近的研究表明,一些古菌和细菌含有替代组蛋白,除了高度分化的序列外,它们还具有不同的 DNA 结合特性。然而,这些组蛋白中的绝大多数是在宏基因组中鉴定出来的,因此很难在体内进行研究。最近的 AlphaFold2 和 RoseTTAfold 计算蛋白质结构预测的革命性突破,使得我们能够以前所未有的方式深入了解以前未被表征的蛋白质的潜在功能和结构。在这里,我们根据 AlphaFold2 的预测,将原核生物的组蛋白空间分为 17 个不同的组。我们确定了一个称为 α3 组蛋白的组蛋白超家族,它在古菌中很常见,并且在几种细菌中存在。重要的是,我们在整个古菌和一些噬菌体中建立了一个大型组蛋白家族的存在,这些组蛋白不缠绕 DNA,而是桥接 DNA,从而与传统的核小体组蛋白不同。