E3 Ligase for CENP-A (Part 1)

Y. Niikura, K. Kitagawa
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Abstract

CENP-A is a centromere-specific histone H3 variant that is required to ensure kinetochore assembly for proper chromosome segregation and its function is highly conserved among different species including budding yeast, Saccharomyces cerevisiae. The budding yeast Saccharomyces cerevisiae has genetically defined point centromeres, unlike other eukaryotes. Although, most eukaryotic centromeres are maintained epigenetically, currently only budding yeast S. cerevisiae centromeres are known to be genetically specified by DNA sequence, The small size and sequence specificity of the budding yeast centromere has made yeast a powerful organism for its study in many aspects. Many post-translational modifications (PTMs) of CENP-A and their functions have been recently reported, and studies with budding yeast are providing insights into the role of CENP-A/Cse4 PTMs in kinetochore structure and function. Multiple functions are controlled especially by ubiquitylation and sumoylation by E3 ligases that control CENP-A protein has initially emerged in the budding yeast as an important regulatory mechanism. Here we focus on what is known about the budding yeast E3 ligases for CENP-A/Cse4 ubiquitylation and sumoylation and their biological functions and significance.
CENP-A的E3连接酶(上)
CENP-A是一种着丝粒特异性组蛋白H3变体,它是确保着丝粒组装以进行适当染色体分离所必需的,其功能在不同物种(包括出芽酵母、酿酒酵母)中高度保守。与其他真核生物不同,出芽酵母酿酒酵母具有遗传上确定的点着丝粒。虽然大多数真核生物的着丝粒都是通过表观遗传方式维持的,但目前已知只有出芽酵母的着丝粒是由DNA序列指定的,出芽酵母的着丝粒体积小,序列特异性强,这使得酵母在许多方面都是一个强有力的研究对象。最近报道了许多CENP-A的翻译后修饰及其功能,对出芽酵母的研究为了解CENP-A/Cse4 PTMs在着丝点结构和功能中的作用提供了新的思路。CENP-A蛋白的多种功能受到E3连接酶的泛素化和sumo化的控制,其在出芽酵母中最初被认为是一个重要的调控机制。本文主要介绍出芽酵母E3连接酶对CENP-A/Cse4泛素化和sumo化的作用及其生物学功能和意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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