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Nuclear phosphatidylinositol 4,5-bisphosphate islets contribute to efficient RNA polymerase II-dependent transcription.

Authors :
Sobol M
Krausová A
Yildirim S
Kalasová I
Fáberová V
Vrkoslav V
Philimonenko V
Marášek P
Pastorek L
Čapek M
Lubovská Z
Uličná L
Tsuji T
Lísa M
Cvačka J
Fujimoto T
Hozak P
Source :
Journal of cell science [J Cell Sci] 2018 Apr 13; Vol. 131 (8). Date of Electronic Publication: 2018 Apr 13.
Publication Year :
2018

Abstract

This paper describes a novel type of nuclear structure - nuclear lipid islets (NLIs). They are of 40-100 nm with a lipidic interior, and phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P <subscript>2</subscript> ] molecules comprise a significant part of their surface. Most of NLIs have RNA at the periphery. Consistent with that, RNA is required for their integrity. The NLI periphery is associated with Pol II transcription machinery, including the largest Pol II subunit, transcription factors and NM1 (also known as NMI). The PtdIns(4,5)P <subscript>2</subscript> -NM1 interaction is important for Pol II transcription, since NM1 knockdown reduces the Pol II transcription level, and the overexpression of wild-type NM1 [but not NM1 mutated in the PtdIns(4,5)P <subscript>2</subscript> -binding site] rescues the transcription. Importantly, Pol II transcription is dependent on NLI integrity, because an enzymatic reduction of the PtdIns(4,5)P <subscript>2</subscript> level results in a decrease of the Pol II transcription level. Furthermore, about half of nascent transcripts localise to NLIs, and transcriptionally active transgene loci preferentially colocalise with NLIs. We hypothesize that NLIs serve as a structural platform that facilitates the formation of Pol II transcription factories, thus participating in the formation of nuclear architecture competent for transcription.<br />Competing Interests: Competing interestsThe authors declare no competing or financial interests.<br /> (© 2018. Published by The Company of Biologists Ltd.)

Details

Language :
English
ISSN :
1477-9137
Volume :
131
Issue :
8
Database :
MEDLINE
Journal :
Journal of cell science
Publication Type :
Academic Journal
Accession number :
29507116
Full Text :
https://doi.org/10.1242/jcs.211094