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...
Autores principales: | , , , , , |
---|---|
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 |