组蛋白H3表观遗传学翻译后修饰的模式由VRK1染色质激酶调节。

IF 4.2 2区 生物学 Q1 GENETICS & HEREDITY
Eva Monte-Serrano, Patricia Morejón-García, Ignacio Campillo-Marcos, Aurora Campos-Díaz, Elena Navarro-Carrasco, Pedro A Lazo
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引用次数: 1

摘要

背景:动态染色质重塑与基于动态染色质重构的过程所需的组蛋白乙酰化和甲基化的表观遗传学模式的变化有关,并与不同的核功能有关。这些组蛋白表观遗传学修饰需要协调,这一作用可能由染色质激酶如VRK1介导,VRK1磷酸化组蛋白H3和H2A,在A549肺腺癌和U2OS骨肉瘤细胞中。结果:染色质组织由不同类型的酶介导的组蛋白磷酸化模式决定。我们已经研究了VRK1染色质激酶如何通过使用该激酶(VRK-IN-1)的特异性抑制剂siRNA、组蛋白乙酰基和甲基转移酶以及组蛋白脱乙酰基酶和去甲基酶来改变组蛋白的表观遗传学翻译后修饰。VRK1的缺失涉及H3K9翻译后修饰状态的转换。VRK1缺失/抑制导致H3K9乙酰化的损失并促进其甲基化。这种效果类似于KAT抑制剂C646的效果,也类似于KDM抑制剂iadademstat(ORY-1001)或JMJD2抑制剂的效果。或者,HDAC抑制剂(selisistat、panobinostat、vorinostat)和国民党抑制剂(tazemetostat、chaetocin)具有与VRK1耗竭或抑制相反的作用,并导致H3K9ac增加和H3K9me3减少。VRK1与这四个酶家族的成员稳定地相互作用。然而,VRK1只能通过间接机制在这些表观遗传学修饰中发挥作用,在间接机制中,这些表观遗传酶可能是VRK1调节和协调的靶点。结论:染色质激酶VRK1调节赖氨酸4、9和27中组蛋白H3乙酰化和甲基化的表观遗传学模式。VRK1是染色质组织的主要调节因子,与其特定功能相关,如转录或DNA修复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The pattern of histone H3 epigenetic posttranslational modifications is regulated by the VRK1 chromatin kinase.

The pattern of histone H3 epigenetic posttranslational modifications is regulated by the VRK1 chromatin kinase.

The pattern of histone H3 epigenetic posttranslational modifications is regulated by the VRK1 chromatin kinase.

The pattern of histone H3 epigenetic posttranslational modifications is regulated by the VRK1 chromatin kinase.

Background: Dynamic chromatin remodeling is associated with changes in the epigenetic pattern of histone acetylations and methylations required for processes based on dynamic chromatin remodeling and implicated in different nuclear functions. These histone epigenetic modifications need to be coordinated, a role that may be mediated by chromatin kinases such as VRK1, which phosphorylates histones H3 and H2A.

Methods: The effect of VRK1 depletion and VRK1 inhibitor, VRK-IN-1, on the acetylation and methylation of histone H3 in K4, K9 and K27 was determined under different conditions, arrested or proliferating cells, in A549 lung adenocarcinoma and U2OS osteosarcoma cells.

Results: Chromatin organization is determined by the phosphorylation pattern of histones mediated by different types of enzymes. We have studied how the VRK1 chromatin kinase can alter the epigenetic posttranslational modifications of histones by using siRNA, a specific inhibitor of this kinase (VRK-IN-1), and of histone acetyl and methyl transferases, as well as histone deacetylase and demethylase. Loss of VRK1 implicated a switch in the state of H3K9 posttranslational modifications. VRK1 depletion/inhibition causes a loss of H3K9 acetylation and facilitates its methylation. This effect is similar to that of the KAT inhibitor C646, and to KDM inhibitors as iadademstat (ORY-1001) or JMJD2 inhibitor. Alternatively, HDAC inhibitors (selisistat, panobinostat, vorinostat) and KMT inhibitors (tazemetostat, chaetocin) have the opposite effect of VRK1 depletion or inhibition, and cause increase of H3K9ac and a decrease of H3K9me3. VRK1 stably interacts with members of these four enzyme families. However, VRK1 can only play a role on these epigenetic modifications by indirect mechanisms in which these epigenetic enzymes are likely targets to be regulated and coordinated by VRK1.

Conclusions: The chromatin kinase VRK1 regulates the epigenetic patterns of histone H3 acetylation and methylation in lysines 4, 9 and 27. VRK1 is a master regulator of chromatin organization associated with its specific functions, such as transcription or DNA repair.

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来源期刊
Epigenetics & Chromatin
Epigenetics & Chromatin GENETICS & HEREDITY-
CiteScore
7.00
自引率
0.00%
发文量
35
审稿时长
1 months
期刊介绍: Epigenetics & Chromatin is a peer-reviewed, open access, online journal that publishes research, and reviews, providing novel insights into epigenetic inheritance and chromatin-based interactions. The journal aims to understand how gene and chromosomal elements are regulated and their activities maintained during processes such as cell division, differentiation and environmental alteration.
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