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ATXN3 通过调节染色质结构控制 DNA 复制和转录。

ATXN3 controls DNA replication and transcription by regulating chromatin structure.

机构信息

Unidad de Investigación, Hospital Universitario de Canarias, La Laguna, Santa Cruz de Tenerife, Spain.

Escuela de Doctorado y Estudios de Posgrado, Universidad de la Laguna, Santa Cruz de Tenerife, Spain.

出版信息

Nucleic Acids Res. 2023 Jun 23;51(11):5396-5413. doi: 10.1093/nar/gkad212.

DOI:10.1093/nar/gkad212
PMID:36971114
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10287915/
Abstract

The deubiquitinating enzyme Ataxin-3 (ATXN3) contains a polyglutamine (PolyQ) region, the expansion of which causes spinocerebellar ataxia type-3 (SCA3). ATXN3 has multiple functions, such as regulating transcription or controlling genomic stability after DNA damage. Here we report the role of ATXN3 in chromatin organization during unperturbed conditions, in a catalytic-independent manner. The lack of ATXN3 leads to abnormalities in nuclear and nucleolar morphology, alters DNA replication timing and increases transcription. Additionally, indicators of more open chromatin, such as increased mobility of histone H1, changes in epigenetic marks and higher sensitivity to micrococcal nuclease digestion were detected in the absence of ATXN3. Interestingly, the effects observed in cells lacking ATXN3 are epistatic to the inhibition or lack of the histone deacetylase 3 (HDAC3), an interaction partner of ATXN3. The absence of ATXN3 decreases the recruitment of endogenous HDAC3 to the chromatin, as well as the HDAC3 nuclear/cytoplasm ratio after HDAC3 overexpression, suggesting that ATXN3 controls the subcellular localization of HDAC3. Importantly, the overexpression of a PolyQ-expanded version of ATXN3 behaves as a null mutant, altering DNA replication parameters, epigenetic marks and the subcellular distribution of HDAC3, giving new insights into the molecular basis of the disease.

摘要

去泛素化酶 Ataxin-3(ATXN3)含有一个多聚谷氨酰胺(PolyQ)区域,该区域的扩展会导致脊髓小脑共济失调 3 型(SCA3)。ATXN3 具有多种功能,如调节转录或控制 DNA 损伤后的基因组稳定性。在这里,我们报告了 ATXN3 在未受干扰的条件下参与染色质组织的作用,这种作用是依赖于其催化活性之外的机制。缺乏 ATXN3 会导致核和核仁形态异常,改变 DNA 复制时间,并增加转录。此外,在缺乏 ATXN3 的情况下,检测到组蛋白 H1 的流动性增加、表观遗传标记的变化和对微球菌核酸酶消化的敏感性增加等更多开放染色质的指标。有趣的是,在缺乏 ATXN3 的细胞中观察到的效应与组蛋白去乙酰化酶 3(HDAC3)的抑制或缺失呈上位性,HDAC3 是 ATXN3 的相互作用伙伴。缺乏 ATXN3 会降低内源性 HDAC3 向染色质的募集,以及 HDAC3 过表达后核/细胞质比值,这表明 ATXN3 控制着 HDAC3 的亚细胞定位。重要的是,多聚谷氨酰胺扩展型 ATXN3 的过表达表现为无效突变体,改变 DNA 复制参数、表观遗传标记和 HDAC3 的亚细胞分布,为该疾病的分子基础提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/de461b37d383/gkad212fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/e9342429722b/gkad212figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/d9ac099f5882/gkad212fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/1d8f6bc77da5/gkad212fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/0f13cff91d41/gkad212fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/69fa7ec1117b/gkad212fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/9b406abc001f/gkad212fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/b3ae508c95f1/gkad212fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/0360cab7c558/gkad212fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/de461b37d383/gkad212fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/e9342429722b/gkad212figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/d9ac099f5882/gkad212fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/1d8f6bc77da5/gkad212fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/0f13cff91d41/gkad212fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/69fa7ec1117b/gkad212fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/9b406abc001f/gkad212fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/b3ae508c95f1/gkad212fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/0360cab7c558/gkad212fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a488/10287915/de461b37d383/gkad212fig8.jpg

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