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旁斑调节与旁斑相关的Ctn RNA在细胞核内的分布。

Paraspeckles modulate the intranuclear distribution of paraspeckle-associated Ctn RNA.

作者信息

Anantharaman Aparna, Jadaliha Mahdieh, Tripathi Vidisha, Nakagawa Shinichi, Hirose Tetsuro, Jantsch Michael F, Prasanth Supriya G, Prasanth Kannanganattu V

机构信息

Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, 601 S Goodwin Avenue, Urbana, IL 61801, USA.

RNA Biology Laboratory, Faculty of Pharmaceutical Sciences, Hokkaido University, Kita 12-jo Nishi 6-chome, Kita-ku, Sapporo 060-0812, Japan.

出版信息

Sci Rep. 2016 Sep 26;6:34043. doi: 10.1038/srep34043.

Abstract

Paraspeckles are sub-nuclear domains that are nucleated by long noncoding RNA Neat1. While interaction of protein components of paraspeckles and Neat1 is understood, there is limited information on the interaction of non-structural RNA components with paraspeckles. Here, by varying paraspeckle number and size, we investigate how paraspeckles influence the nuclear organization of their non-structural RNA component Ctn RNA. Our results show that Ctn RNA remains nuclear-retained in the absence of intact paraspeckles, suggesting that they do not regulate nuclear retention of Ctn RNA. In the absence of Neat1, Ctn RNA continues to interact with paraspeckle protein NonO to form residual nuclear foci. In addition, in the absence of Neat1-nucleated paraspeckles, a subset of Ctn RNA localizes to the perinucleolar regions. Concomitant with increase in number of paraspeckles, transcriptional reactivation resulted in increased number of paraspeckle-localized Ctn RNA foci. Similar to Neat1, proteasome inhibition altered the localization of Ctn RNA, where it formed enlarged paraspeckle-like foci. Super-resolution structured illumination microscopic analyses revealed that in paraspeckles, Ctn RNA partially co-localized with Neat1, and displayed a more heterogeneous intra-paraspeckle localization. Collectively, these results show that while paraspeckles do not influence nuclear retention of Ctn RNA, they modulate its intranuclear compartmentalization.

摘要

副斑点是由长链非编码RNA Neat1成核的亚核结构域。虽然副斑点的蛋白质成分与Neat1之间的相互作用已为人所知,但关于非结构RNA成分与副斑点相互作用的信息却很有限。在这里,我们通过改变副斑点的数量和大小,研究副斑点如何影响其非结构RNA成分Ctn RNA的核组织。我们的结果表明,在没有完整副斑点的情况下,Ctn RNA仍保留在细胞核中,这表明它们不调节Ctn RNA的核保留。在没有Neat1的情况下,Ctn RNA继续与副斑点蛋白NonO相互作用,形成残留的核灶。此外,在没有Neat1成核的副斑点的情况下,一部分Ctn RNA定位于核仁周围区域。随着副斑点数量的增加,转录激活导致副斑点定位的Ctn RNA灶数量增加。与Neat1相似,蛋白酶体抑制改变了Ctn RNA的定位,使其形成扩大的副斑点样灶。超分辨率结构照明显微镜分析显示,在副斑点中,Ctn RNA与Neat1部分共定位,并在副斑点内显示出更不均匀的定位。总的来说,这些结果表明,虽然副斑点不影响Ctn RNA的核保留,但它们调节其核内分隔。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7243/5036046/8f1decae587f/srep34043-f1.jpg

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