Instituto Gulbenkian de Ciência, 2780-156 Oeiras, Portugal.
Chromosome Res. 2012 Jul;20(5):481-92. doi: 10.1007/s10577-012-9291-2.
All living organisms require accurate mechanisms to faithfully inherit their genetic material during cell division. The centromere is a unique locus on each chromosome that supports a multiprotein structure called the kinetochore. During mitosis, the kinetochore is responsible for connecting chromosomes to spindle microtubules, allowing faithful segregation of the duplicated genome. In most organisms, centromere position and function is not defined by the local DNA sequence context but rather by an epigenetic chromatin-based mechanism. Centromere protein A (CENP-A) is central to this process, as chromatin assembled from this histone H3 variant is essential for assembly of the centromere complex, as well as for its epigenetic maintenance. As a major determinant of centromere function, CENP-A assembly requires tight control, both in its specificity for the centromere and in timing of assembly. In the last few years, there have been several new insights into the molecular mechanism that allow this process to occur. We will review these here and discuss the general implications of the mechanism of cell cycle coupling of centromere inheritance.
所有生物在细胞分裂过程中都需要精确的机制来忠实地遗传其遗传物质。着丝粒是每条染色体上的一个独特位点,支持称为动粒的多蛋白结构。在有丝分裂过程中,动粒负责将染色体连接到纺锤体微管上,从而实现复制基因组的准确分离。在大多数生物体中,着丝粒的位置和功能不是由局部 DNA 序列上下文定义的,而是由基于表观遗传学染色质的机制定义的。着丝粒蛋白 A (CENP-A) 是这个过程的核心,因为由这种组蛋白 H3 变体组装而成的染色质对于组装着丝粒复合物以及其表观遗传维持至关重要。作为着丝粒功能的主要决定因素,CENP-A 组装需要严格控制,既要特异性地针对着丝粒,又要控制组装的时间。在过去的几年中,人们对允许这一过程发生的分子机制有了一些新的认识。我们将在这里回顾这些内容,并讨论细胞周期偶联的机制对中心粒遗传的普遍影响。