Ghosal Debnath, Löwe Jan
MRC Laboratory of Molecular Biology, Cambridge, UK
MRC Laboratory of Molecular Biology, Cambridge, UK.
EMBO J. 2015 Sep 14;34(18):2312-20. doi: 10.15252/embj.201591756. Epub 2015 Aug 12.
It is now well established that prokaryotic cells assemble diverse proteins into dynamic cytoskeletal filaments that perform essential cellular functions. Although most of the filaments assemble on their own to form higher order structures, growing evidence suggests that there are a number of prokaryotic proteins that polymerise only in the presence of a matrix such as DNA, lipid membrane or even another filament. Matrix-assisted filament systems are frequently nucleotide dependent and cytomotive but rarely considered as part of the bacterial cytoskeleton. Here, we categorise this family of filament-forming systems as collaborative filaments and introduce a simple nomenclature. Collaborative filaments are frequent in both eukaryotes and prokaryotes and are involved in vital cellular processes including chromosome segregation, DNA repair and maintenance, gene silencing and cytokinesis to mention a few. In this review, we highlight common principles underlying collaborative filaments and correlate these with known functions.
现在已经充分证实,原核细胞将多种蛋白质组装成动态的细胞骨架细丝,这些细丝执行基本的细胞功能。尽管大多数细丝能自行组装形成更高阶的结构,但越来越多的证据表明,有许多原核蛋白质仅在诸如DNA、脂质膜甚至另一细丝等基质存在的情况下才会聚合。基质辅助细丝系统通常依赖核苷酸且具有细胞运动性,但很少被视为细菌细胞骨架的一部分。在这里,我们将这一细丝形成系统家族归类为协作细丝,并引入一种简单的命名法。协作细丝在真核生物和原核生物中都很常见,并且参与重要的细胞过程,包括染色体分离、DNA修复与维持、基因沉默和胞质分裂等等。在这篇综述中,我们强调协作细丝背后的共同原理,并将这些原理与已知功能联系起来。