Cargando…

LncRNA AK023948 is a positive regulator of AKT

Despite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little is known about their physiological functions for the majority of them. The present study uses a CRISPR/Cas9-based synergistic activation mediator (SAM) system to identify potential lncRNAs capable of regu...

Descripción completa

Detalles Bibliográficos
Autores principales: Koirala, Pratirodh, Huang, Jianguo, Ho, Tsui-Ting, Wu, Fangting, Ding, Xianfeng, Mo, Yin-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309785/
https://www.ncbi.nlm.nih.gov/pubmed/28176758
http://dx.doi.org/10.1038/ncomms14422
_version_ 1782507766849470464
author Koirala, Pratirodh
Huang, Jianguo
Ho, Tsui-Ting
Wu, Fangting
Ding, Xianfeng
Mo, Yin-Yuan
author_facet Koirala, Pratirodh
Huang, Jianguo
Ho, Tsui-Ting
Wu, Fangting
Ding, Xianfeng
Mo, Yin-Yuan
author_sort Koirala, Pratirodh
collection PubMed
description Despite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little is known about their physiological functions for the majority of them. The present study uses a CRISPR/Cas9-based synergistic activation mediator (SAM) system to identify potential lncRNAs capable of regulating AKT activity. Among lncRNAs identified from this screen, we demonstrate that AK023948 is a positive regulator for AKT. Knockout of AK023948 suppresses, whereas rescue with AK023948 restores the AKT activity. Mechanistically, AK023948 functionally interacts with DHX9 and p85. Importantly, AK023948 is required for the interaction between DHX9 and p85 to hence the p85 stability and promote AKT activity. Finally, AK023948 is upregulated in breast cancer; interrogation of TCGA data set indicates that upregulation of DHX9 in breast cancer is associated with poor survival. Together, this study demonstrates two previously uncharacterized factors AK023948 and DHX9 as important players in the AKT pathway, and that their upregulation may contribute to breast tumour progression.
format Online
Article
Text
id pubmed-5309785
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-53097852017-02-27 LncRNA AK023948 is a positive regulator of AKT Koirala, Pratirodh Huang, Jianguo Ho, Tsui-Ting Wu, Fangting Ding, Xianfeng Mo, Yin-Yuan Nat Commun Article Despite the overwhelming number of human long non-coding RNAs (lncRNAs) reported so far, little is known about their physiological functions for the majority of them. The present study uses a CRISPR/Cas9-based synergistic activation mediator (SAM) system to identify potential lncRNAs capable of regulating AKT activity. Among lncRNAs identified from this screen, we demonstrate that AK023948 is a positive regulator for AKT. Knockout of AK023948 suppresses, whereas rescue with AK023948 restores the AKT activity. Mechanistically, AK023948 functionally interacts with DHX9 and p85. Importantly, AK023948 is required for the interaction between DHX9 and p85 to hence the p85 stability and promote AKT activity. Finally, AK023948 is upregulated in breast cancer; interrogation of TCGA data set indicates that upregulation of DHX9 in breast cancer is associated with poor survival. Together, this study demonstrates two previously uncharacterized factors AK023948 and DHX9 as important players in the AKT pathway, and that their upregulation may contribute to breast tumour progression. Nature Publishing Group 2017-02-08 /pmc/articles/PMC5309785/ /pubmed/28176758 http://dx.doi.org/10.1038/ncomms14422 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Koirala, Pratirodh
Huang, Jianguo
Ho, Tsui-Ting
Wu, Fangting
Ding, Xianfeng
Mo, Yin-Yuan
LncRNA AK023948 is a positive regulator of AKT
title LncRNA AK023948 is a positive regulator of AKT
title_full LncRNA AK023948 is a positive regulator of AKT
title_fullStr LncRNA AK023948 is a positive regulator of AKT
title_full_unstemmed LncRNA AK023948 is a positive regulator of AKT
title_short LncRNA AK023948 is a positive regulator of AKT
title_sort lncrna ak023948 is a positive regulator of akt
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309785/
https://www.ncbi.nlm.nih.gov/pubmed/28176758
http://dx.doi.org/10.1038/ncomms14422
work_keys_str_mv AT koiralapratirodh lncrnaak023948isapositiveregulatorofakt
AT huangjianguo lncrnaak023948isapositiveregulatorofakt
AT hotsuiting lncrnaak023948isapositiveregulatorofakt
AT wufangting lncrnaak023948isapositiveregulatorofakt
AT dingxianfeng lncrnaak023948isapositiveregulatorofakt
AT moyinyuan lncrnaak023948isapositiveregulatorofakt