Serebryannyy Leonid A, Yuen Michaela, Parilla Megan, Cooper Sandra T, de Lanerolle Primal
Department of Physiology and Biophysics, University of Illinois at Chicago Chicago, IL, USA.
Institute for Neuroscience and Muscle Research, Kids Research Institute, The Children's Hospital at WestmeadSydney, NSW, Australia; Faculty of Medicine, Discipline of Pediatrics and Child Health, University of SydneySydney, NSW, Australia.
Front Physiol. 2016 Oct 7;7:454. doi: 10.3389/fphys.2016.00454. eCollection 2016.
Actin plays a crucial role in regulating multiple processes within the nucleus, including transcription and chromatin organization. However, the polymerization state of nuclear actin remains controversial, and there is no evidence for persistent actin filaments in a normal interphase nucleus. Further, several disease pathologies are characterized by polymerization of nuclear actin into stable filaments or rods. These include filaments that stain with phalloidin, resulting from point mutations in skeletal α-actin, detected in the human skeletal disease intranuclear rod myopathy, and cofilin/actin rods that form in response to cellular stressors like heatshock. To further elucidate the effects of these pathological actin structures, we examined the nucleus in both cell culture models as well as isolated human tissues. We find these actin structures alter the distribution of both RNA polymerase II and chromatin. Our data suggest that nuclear actin filaments result in disruption of nuclear organization, which may contribute to the disease pathology.
肌动蛋白在调节细胞核内的多种过程中发挥着关键作用,包括转录和染色质组织。然而,核肌动蛋白的聚合状态仍存在争议,并且没有证据表明在正常间期核中有持续存在的肌动蛋白丝。此外,几种疾病病理学特征是核肌动蛋白聚合成稳定的丝或杆。这些包括在人类骨骼疾病核内杆状肌病中检测到的,由骨骼α-肌动蛋白点突变导致的用鬼笔环肽染色的丝,以及响应热休克等细胞应激源形成的丝切蛋白/肌动蛋白杆。为了进一步阐明这些病理性肌动蛋白结构的影响,我们在细胞培养模型以及分离的人体组织中研究了细胞核。我们发现这些肌动蛋白结构改变了RNA聚合酶II和染色质的分布。我们的数据表明,核肌动蛋白丝导致核组织的破坏,这可能导致疾病病理学。