Department of Pathology, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Department of Pathology, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Biochem Biophys Res Commun. 2014 Apr 18;446(4):1268-75. doi: 10.1016/j.bbrc.2014.03.114. Epub 2014 Mar 29.
Dyskerin is a conserved, nucleolar RNA-binding protein implicated in an increasing array of fundamental cellular processes. Germline mutation in the dyskerin gene (DKC1) is the cause of X-linked dyskeratosis congenita (DC). Conversely, wild-type dyskerin is overexpressed in sporadic cancers, and high-levels may be associated with poor prognosis. It was previously reported that acute loss of dyskerin function via siRNA-mediated depletion slowed the proliferation of transformed cell lines. However, the mechanisms remained unclear. Using human U2OS osteosarcoma cells, we show that siRNA-mediated dyskerin depletion induced cellular senescence as evidenced by proliferative arrest, senescence-associated heterochromatinization and a senescence-associated molecular profile. Senescence can render cells resistant to apoptosis. Conversely, chromatin relaxation can reverse the repressive effects of senescence-associated heterochromatinization on apoptosis. To this end, genotoxic stress-induced apoptosis was suppressed in dyskerin-depleted cells. In contrast, agents that induce chromatin relaxation, including histone deacetylase inhibitors and the DNA intercalator chloroquine, sensitized dyskerin-depleted cells to apoptosis. Dyskerin is a core component of the telomerase complex and plays an important role in telomere homeostasis. Defective telomere maintenance resulting in premature senescence is thought to primarily underlie the pathogenesis of X-linked DC. Since U2OS cells are telomerase-negative, this leads us to conclude that loss of dyskerin function can also induce cellular senescence via mechanisms independent of telomere shortening.
核仁蛋白 dyskerin 是一种保守的 RNA 结合蛋白,涉及越来越多的基本细胞过程。dyskerin 基因(DKC1)的种系突变是 X 连锁先天性角化不良(DC)的原因。相反,散发性癌症中野生型 dyskerin 过表达,高水平可能与预后不良相关。先前的研究表明,通过 siRNA 介导的耗竭急性丧失 dyskerin 功能会减缓转化细胞系的增殖。然而,其机制尚不清楚。使用人 U2OS 骨肉瘤细胞,我们表明 siRNA 介导的 dyskerin 耗竭诱导细胞衰老,表现为增殖停滞、衰老相关异染色质化和衰老相关的分子特征。衰老可以使细胞对凋亡产生抗性。相反,染色质松弛可以逆转衰老相关异染色质化对凋亡的抑制作用。为此,在 dyskerin 耗竭细胞中,遗传毒性应激诱导的细胞凋亡受到抑制。相比之下,诱导染色质松弛的试剂,包括组蛋白去乙酰化酶抑制剂和 DNA 嵌入剂氯喹,使 dyskerin 耗竭细胞对凋亡敏感。Dyskerin 是端粒酶复合物的核心组成部分,在端粒稳态中发挥重要作用。缺陷的端粒维持导致过早衰老,被认为是 X 连锁 DC 发病机制的主要原因。由于 U2OS 细胞缺乏端粒酶,这使我们得出结论,dyskerin 功能的丧失也可以通过独立于端粒缩短的机制诱导细胞衰老。