Della Fera Ashley N, Arman Warda, Powers Maceo E, Warburton Alix, McBride Alison A
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
bioRxiv. 2025 Mar 6:2025.03.06.641437. doi: 10.1101/2025.03.06.641437.
PML nuclear bodies (PML-NBs) are dynamic subnuclear structures important for chromatin dynamics and anti-viral defense. In this study we investigate the role of Sp100 isoforms in promoting localization of the H3.3 histone chaperone HIRA to PML-NBs in human keratinocytes. Sp100 knockout (KO) cell lines were generated using CRISPR-Cas9 technology and shown to display normal keratinocyte differentiation and PML-NB formation. However, HIRA and its associated complex members (UBN1 and ASF1a) failed to localize to PML-NBs in the absence of Sp100, even after interferon stimulation. Exogenous expression of the four main isoforms of Sp100 showed that the Sp100A isoform is the primary driver of HIRA localization to PML-NBs, with the SUMO interacting motif (SIM) playing an important role. These findings highlight the functional diversity of the Sp100 isoforms in modulating chromatin dynamics at PML-NBs.
早幼粒细胞白血病核体(PML-NBs)是对染色质动态变化和抗病毒防御很重要的动态亚核结构。在本研究中,我们调查了Sp100亚型在促进组蛋白伴侣H3.3的HIRA定位于人角质形成细胞中的PML-NBs方面的作用。使用CRISPR-Cas9技术构建了Sp100基因敲除(KO)细胞系,结果显示其角质形成细胞分化和PML-NB形成正常。然而,在没有Sp100的情况下,即使在干扰素刺激后,HIRA及其相关复合物成员(UBN1和ASF1a)也无法定位于PML-NBs。Sp100四种主要亚型的外源表达表明,Sp100A亚型是HIRA定位于PML-NBs的主要驱动因素,其中小泛素样修饰物相互作用基序(SIM)发挥着重要作用。这些发现突出了Sp100亚型在调节PML-NBs处染色质动态变化方面的功能多样性。