Roy Babhrubahan, Sanyal Kaustuv
Molecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.
Eukaryot Cell. 2011 Nov;10(11):1384-95. doi: 10.1128/EC.05165-11. Epub 2011 Sep 9.
A centromere is a chromosomal region on which several proteins assemble to form the kinetochore. The centromere-kinetochore complex helps in the attachment of chromosomes to spindle microtubules to mediate segregation of chromosomes to daughter cells during mitosis and meiosis. In several budding yeast species, the centromere forms in a DNA sequence-dependent manner, whereas in most other fungi, factors other than the DNA sequence also determine the centromere location, as centromeres were able to form on nonnative sequences (neocentromeres) when native centromeres were deleted in engineered strains. Thus, in the absence of a common DNA sequence, the cues that have facilitated centromere formation on a specific DNA sequence for millions of years remain a mystery. Kinetochore formation is facilitated by binding of a centromere-specific histone protein member of the centromeric protein A (CENP-A) family that replaces a canonical histone H3 to form a specialized centromeric chromatin structure. However, the process of kinetochore formation on the rapidly evolving and seemingly diverse centromere DNAs in different fungal species is largely unknown. More interestingly, studies in various yeasts suggest that the factors required for de novo centromere formation (establishment) may be different from those required for maintenance (propagation) of an already established centromere. Apart from the DNA sequence and CENP-A, many other factors, such as posttranslational modification (PTM) of histones at centric and pericentric chromatin, RNA interference, and DNA methylation, are also involved in centromere formation, albeit in a species-specific manner. In this review, we discuss how several genetic and epigenetic factors influence the evolution of structure and function of centromeres in fungal species.
着丝粒是一个染色体区域,几种蛋白质在其上组装形成动粒。着丝粒 - 动粒复合体有助于将染色体附着到纺锤体微管上,从而在有丝分裂和减数分裂期间介导染色体向子细胞的分离。在几种芽殖酵母物种中,着丝粒以依赖于DNA序列的方式形成,而在大多数其他真菌中,除了DNA序列之外的其他因素也决定着丝粒的位置,因为在工程菌株中删除天然着丝粒时,着丝粒能够在非天然序列(新着丝粒)上形成。因此,在没有共同DNA序列的情况下,数百万年来促进着丝粒在特定DNA序列上形成的线索仍然是个谜。着丝粒特异性组蛋白CENP - A家族成员的结合促进了动粒的形成,该成员取代了经典组蛋白H3以形成特殊的着丝粒染色质结构。然而,在不同真菌物种中快速进化且看似多样的着丝粒DNA上形成动粒的过程在很大程度上尚不清楚。更有趣的是,对各种酵母的研究表明,从头形成(建立)着丝粒所需的因素可能与维持(传播)已建立的着丝粒所需的因素不同。除了DNA序列和CENP - A之外,许多其他因素,如着丝粒和着丝粒周围染色质上组蛋白的翻译后修饰(PTM)、RNA干扰和DNA甲基化,也参与着丝粒的形成,尽管是以物种特异性的方式。在这篇综述中,我们讨论了几种遗传和表观遗传因素如何影响真菌物种着丝粒的结构和功能进化。