Dipartimento di Biologia e Biotecnologie "Charles Darwin", Sapienza Università di Roma, Rome, Italy.
Universita degli Studi di Milano-Bicocca, Piazza dell' Ateneo Nuovo, 1, 20126, Milano, Italy.
Cell Mol Life Sci. 2023 Nov 20;80(12):365. doi: 10.1007/s00018-023-04949-8.
The aim of this review article is to focus on the unconventional roles of epigenetic players (chromatin remodelers and long non-coding RNAs) in cell division, beyond their well-characterized functions in chromatin regulation during cell differentiation and development. In the last two decades, diverse experimental evidence has shown that subunits of SRCAP and p400/TIP60 chromatin remodeling complexes in humans relocate from interphase nuclei to centrosomes, spindle or midbody, with their depletion yielding an array of aberrant outcomes of mitosis and cytokinesis. Remarkably, this behavior is shared by orthologous subunits of the Drosophila melanogaster DOM/TIP60 complex, despite fruit flies and humans diverged over 700 million years ago. In short, the available data support the view that subunits of these complexes are a new class of moonlighting proteins, in that they lead a "double life": during the interphase, they function in chromatin regulation within the nucleus, but as the cell progresses through mitosis, they interact with established mitotic factors, thus becoming integral components of the cell division apparatus. By doing so, they contribute to ensuring the correct distribution of chromosomes in the two daughter cells and, when dysfunctional, can cause genomic instability, a condition that can trigger tumorigenesis and developmental diseases. Research over the past few years has unveiled a major contribution of long non-coding RNAs (lncRNAs) in the epigenetics regulation of gene expression which also impacts on cell division control. Here, we focus on possible structural roles of lncRNAs in the execution of cytokinesis: in particular, we suggest that specific classes of lncRNAs relocate to the midbody to form an architectural scaffold ensuring its proper assembly and function during abscission. Drawing attention to experimental evidence for non-canonical extranuclear roles of chromatin factors and lncRNAs has direct implications on important and novel aspects concerning both the epigenetic regulation and the evolutionary dynamics of cell division with a significant impact on differentiation, development, and diseases.
本文的目的是关注表观遗传因子(染色质重塑因子和长链非编码 RNA)在细胞分裂中的非常规作用,超越它们在细胞分化和发育过程中染色质调控方面的作用。在过去的二十年中,各种实验证据表明,人类 SRCAP 和 p400/TIP60 染色质重塑复合物的亚基从间期核迁移到中心体、纺锤体或中间体,其耗竭会导致有丝分裂和胞质分裂的一系列异常后果。值得注意的是,尽管果蝇和人类在 7 亿多年前就已经分化,但果蝇同源的 DOM/TIP60 复合物的亚基也有这种行为。简而言之,现有数据支持这样一种观点,即这些复合物的亚基是一类新的 moonlighting 蛋白,因为它们过着“双重生活”:在间期,它们在核内的染色质调控中发挥作用,但随着细胞进入有丝分裂,它们与已建立的有丝分裂因子相互作用,从而成为细胞分裂装置的组成部分。通过这种方式,它们有助于确保染色体在两个子细胞中的正确分配,而当它们功能失调时,可能会导致基因组不稳定,这种情况可能会引发肿瘤发生和发育疾病。过去几年的研究揭示了长链非编码 RNA(lncRNA)在基因表达的表观遗传调控中发挥了重要作用,也影响细胞分裂的控制。在这里,我们重点关注 lncRNA 在胞质分裂执行中的可能结构作用:特别是,我们提出特定类别的 lncRNA 迁移到中间体,形成一个结构支架,确保其在分裂过程中的正确组装和功能。关注染色质因子和 lncRNA 的非典型核外作用的实验证据,对表观遗传调控和细胞分裂的进化动态的重要和新颖方面具有直接影响,对分化、发育和疾病有重大影响。