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着丝粒的表观遗传调控:我们能从新着丝粒中学到什么?

Epigenetic control of centromere: what can we learn from neocentromere?

作者信息

Kim Taekyung

机构信息

Department of Biology Education, Pusan National University, 2, Busandaehak-ro 63beon-gil, Geumjeong-gu, Busan, 46241, Korea.

出版信息

Genes Genomics. 2022 Mar;44(3):317-325. doi: 10.1007/s13258-021-01193-x. Epub 2021 Nov 29.

Abstract

BACKGROUND

The centromere is the special region on a chromosome, which serves as the site for assembly of kinetochore complex and is essential for maintaining genomic integrity. Neocentromeres are new centromeres that form on the non-centromeric regions of the chromosome when the natural centromere is disrupted or inactivated. Although neocentromeres lack the typical features found in centromeres, cells with neocentromeres divide normally during mitosis and meiosis. Neocentromeres not only arise naturally but their formation can also be induced experimentally. Therefore, neocentromeres are a great tool for studying functions and formation of centromeres.

OBJECTIVE

To study neocentromeres and use that knowledge to gain insights into the epigenetic regulation of canonical centromeres.

DISCUSSION

Here, we review the characteristics of naturally occurring centromeres and neocentromeres and those of experimentally induced neocentromeres. We also discuss the mechanism of centromere formation and epigenetic regulation of centromere function, which we learned from studying the neocentromeres. Although neocentromeres lack main features of centromeres, such as presence of repetitive ⍺-satellite DNA and pericentric heterochromatin, they behave quite similar to the canonical centromere, indicating the epigenetic nature of the centromere. Still, further investigation will help to understand the formation and maintenance of the centromere, and the correlation to human diseases.

CONCLUSION

Neocentromeres helped us to understand the formation of canonical centromeres. Also, since neocentromeres are associated with certain cancer types, knowledge about them could be helpful to treat cancer.

摘要

背景

着丝粒是染色体上的特殊区域,它作为动粒复合体组装的位点,对于维持基因组完整性至关重要。新着丝粒是在天然着丝粒被破坏或失活时,在染色体的非着丝粒区域形成的新的着丝粒。尽管新着丝粒缺乏着丝粒中发现的典型特征,但具有新着丝粒的细胞在有丝分裂和减数分裂期间能正常分裂。新着丝粒不仅自然产生,其形成也可通过实验诱导。因此,新着丝粒是研究着丝粒功能和形成的有力工具。

目的

研究新着丝粒,并利用这些知识深入了解典型着丝粒的表观遗传调控。

讨论

在此,我们综述了天然存在的着丝粒和新着丝粒以及实验诱导的新着丝粒的特征。我们还讨论了从研究新着丝粒中学到的着丝粒形成机制和着丝粒功能的表观遗传调控。尽管新着丝粒缺乏着丝粒的主要特征,如重复的α卫星DNA和着丝粒周围异染色质的存在,但它们的行为与典型着丝粒非常相似,这表明着丝粒的表观遗传性质。不过,进一步的研究将有助于理解着丝粒的形成和维持,以及与人类疾病的关联。

结论

新着丝粒帮助我们理解了典型着丝粒的形成。此外,由于新着丝粒与某些癌症类型相关,关于它们的知识可能有助于治疗癌症。

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