The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells
Abstract In recent years, long non-coding RNA (lncRNA) research has identified essential roles of these transcripts in virtually all physiological cellular processes including tumorigenesis, but their functions and molecular mechanisms are poorly understood. In this study, we performed a high-throug...
Guardado en:
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/0128d3ba3b3d4231913c4de6607365c4 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:0128d3ba3b3d4231913c4de6607365c4 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:0128d3ba3b3d4231913c4de6607365c42021-12-02T12:32:30ZThe long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells10.1038/s41598-017-02357-02045-2322https://doaj.org/article/0128d3ba3b3d4231913c4de6607365c42017-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-02357-0https://doaj.org/toc/2045-2322Abstract In recent years, long non-coding RNA (lncRNA) research has identified essential roles of these transcripts in virtually all physiological cellular processes including tumorigenesis, but their functions and molecular mechanisms are poorly understood. In this study, we performed a high-throughput siRNA screen targeting 638 lncRNAs deregulated in cancer entities to analyse their impact on cell division by using time-lapse microscopy. We identified 26 lncRNAs affecting cell morphology and cell cycle including LINC00152. This transcript was ubiquitously expressed in many human cell lines and its RNA levels were significantly upregulated in lung, liver and breast cancer tissues. A comprehensive sequence analysis of LINC00152 revealed a highly similar paralog annotated as MIR4435-2HG and several splice variants of both transcripts. The shortest and most abundant isoform preferentially localized to the cytoplasm. Cells depleted of LINC00152 arrested in prometaphase of mitosis and showed reduced cell viability. In RNA affinity purification (RAP) studies, LINC00152 interacted with a network of proteins that were associated with M phase of the cell cycle. In summary, we provide new insights into the properties and biological function of LINC00152 suggesting that this transcript is crucial for cell cycle progression through mitosis and thus, could act as a non-coding oncogene.Linda NötzoldLukas FrankMinakshi GandhiMaria Polycarpou-SchwarzMatthias GroßManuel GunkelNina BeilHolger ErfleNathalie HarderKarl RohrJakob TrendelJeroen KrijgsveldThomas LongerichPeter SchirmacherMichael BoutrosSylvia ErhardtSven DiederichsNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Linda Nötzold Lukas Frank Minakshi Gandhi Maria Polycarpou-Schwarz Matthias Groß Manuel Gunkel Nina Beil Holger Erfle Nathalie Harder Karl Rohr Jakob Trendel Jeroen Krijgsveld Thomas Longerich Peter Schirmacher Michael Boutros Sylvia Erhardt Sven Diederichs The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells |
description |
Abstract In recent years, long non-coding RNA (lncRNA) research has identified essential roles of these transcripts in virtually all physiological cellular processes including tumorigenesis, but their functions and molecular mechanisms are poorly understood. In this study, we performed a high-throughput siRNA screen targeting 638 lncRNAs deregulated in cancer entities to analyse their impact on cell division by using time-lapse microscopy. We identified 26 lncRNAs affecting cell morphology and cell cycle including LINC00152. This transcript was ubiquitously expressed in many human cell lines and its RNA levels were significantly upregulated in lung, liver and breast cancer tissues. A comprehensive sequence analysis of LINC00152 revealed a highly similar paralog annotated as MIR4435-2HG and several splice variants of both transcripts. The shortest and most abundant isoform preferentially localized to the cytoplasm. Cells depleted of LINC00152 arrested in prometaphase of mitosis and showed reduced cell viability. In RNA affinity purification (RAP) studies, LINC00152 interacted with a network of proteins that were associated with M phase of the cell cycle. In summary, we provide new insights into the properties and biological function of LINC00152 suggesting that this transcript is crucial for cell cycle progression through mitosis and thus, could act as a non-coding oncogene. |
format |
article |
author |
Linda Nötzold Lukas Frank Minakshi Gandhi Maria Polycarpou-Schwarz Matthias Groß Manuel Gunkel Nina Beil Holger Erfle Nathalie Harder Karl Rohr Jakob Trendel Jeroen Krijgsveld Thomas Longerich Peter Schirmacher Michael Boutros Sylvia Erhardt Sven Diederichs |
author_facet |
Linda Nötzold Lukas Frank Minakshi Gandhi Maria Polycarpou-Schwarz Matthias Groß Manuel Gunkel Nina Beil Holger Erfle Nathalie Harder Karl Rohr Jakob Trendel Jeroen Krijgsveld Thomas Longerich Peter Schirmacher Michael Boutros Sylvia Erhardt Sven Diederichs |
author_sort |
Linda Nötzold |
title |
The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells |
title_short |
The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells |
title_full |
The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells |
title_fullStr |
The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells |
title_full_unstemmed |
The long non-coding RNA LINC00152 is essential for cell cycle progression through mitosis in HeLa cells |
title_sort |
long non-coding rna linc00152 is essential for cell cycle progression through mitosis in hela cells |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/0128d3ba3b3d4231913c4de6607365c4 |
work_keys_str_mv |
AT lindanotzold thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT lukasfrank thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT minakshigandhi thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT mariapolycarpouschwarz thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT matthiasgroß thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT manuelgunkel thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT ninabeil thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT holgererfle thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT nathalieharder thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT karlrohr thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT jakobtrendel thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT jeroenkrijgsveld thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT thomaslongerich thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT peterschirmacher thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT michaelboutros thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT sylviaerhardt thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT svendiederichs thelongnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT lindanotzold longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT lukasfrank longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT minakshigandhi longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT mariapolycarpouschwarz longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT matthiasgroß longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT manuelgunkel longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT ninabeil longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT holgererfle longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT nathalieharder longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT karlrohr longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT jakobtrendel longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT jeroenkrijgsveld longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT thomaslongerich longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT peterschirmacher longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT michaelboutros longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT sylviaerhardt longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells AT svendiederichs longnoncodingrnalinc00152isessentialforcellcycleprogressionthroughmitosisinhelacells |
_version_ |
1718394016649707520 |