A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.

Numerous genetic and epigenetic alterations render cancer cells selectively dependent on specific genes and regulatory pathways, and represent potential vulnerabilities that can be therapeutically exploited. Here we describe an RNA interference (RNAi)-based synthetic interaction screen to identify g...

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Main Authors: Li Xie, Claude Gazin, Sung Mi Park, Lihua J Zhu, Marie-anne Debily, Ellen L W Kittler, Maria L Zapp, David Lapointe, Stephane Gobeil, Ching-Man Virbasius, Michael R Green
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003151&type=printable
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author Li Xie
Claude Gazin
Sung Mi Park
Lihua J Zhu
Marie-anne Debily
Ellen L W Kittler
Maria L Zapp
David Lapointe
Stephane Gobeil
Ching-Man Virbasius
Michael R Green
author_facet Li Xie
Claude Gazin
Sung Mi Park
Lihua J Zhu
Marie-anne Debily
Ellen L W Kittler
Maria L Zapp
David Lapointe
Stephane Gobeil
Ching-Man Virbasius
Michael R Green
author_sort Li Xie
collection DOAJ
description Numerous genetic and epigenetic alterations render cancer cells selectively dependent on specific genes and regulatory pathways, and represent potential vulnerabilities that can be therapeutically exploited. Here we describe an RNA interference (RNAi)-based synthetic interaction screen to identify genes preferentially required for proliferation of p53-deficient (p53-) human cancer cells. We find that compared to p53-competent (p53+) human cancer cell lines, diverse p53- human cancer cell lines are preferentially sensitive to loss of the transcription factor ETV1 and the DNA damage kinase ATR. In p53- cells, RNAi-mediated knockdown of ETV1 or ATR results in decreased expression of the telomerase catalytic subunit TERT leading to growth arrest, which can be reversed by ectopic TERT expression. Chromatin immunoprecipitation analysis reveals that ETV1 binds to a region downstream of the TERT transcriptional start-site in p53- but not p53+ cells. We find that the role of ATR is to phosphorylate and thereby stabilize ETV1. Our collective results identify a regulatory pathway involving ETV1, ATR, and TERT that is preferentially important for proliferation of diverse p53- cancer cells.
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spelling doaj-art-11c6cc1ae4eb4d4cb2683ba84f2eb5312025-08-20T02:15:30ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042012-01-01812e100315110.1371/journal.pgen.1003151A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.Li XieClaude GazinSung Mi ParkLihua J ZhuMarie-anne DebilyEllen L W KittlerMaria L ZappDavid LapointeStephane GobeilChing-Man VirbasiusMichael R GreenNumerous genetic and epigenetic alterations render cancer cells selectively dependent on specific genes and regulatory pathways, and represent potential vulnerabilities that can be therapeutically exploited. Here we describe an RNA interference (RNAi)-based synthetic interaction screen to identify genes preferentially required for proliferation of p53-deficient (p53-) human cancer cells. We find that compared to p53-competent (p53+) human cancer cell lines, diverse p53- human cancer cell lines are preferentially sensitive to loss of the transcription factor ETV1 and the DNA damage kinase ATR. In p53- cells, RNAi-mediated knockdown of ETV1 or ATR results in decreased expression of the telomerase catalytic subunit TERT leading to growth arrest, which can be reversed by ectopic TERT expression. Chromatin immunoprecipitation analysis reveals that ETV1 binds to a region downstream of the TERT transcriptional start-site in p53- but not p53+ cells. We find that the role of ATR is to phosphorylate and thereby stabilize ETV1. Our collective results identify a regulatory pathway involving ETV1, ATR, and TERT that is preferentially important for proliferation of diverse p53- cancer cells.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003151&type=printable
spellingShingle Li Xie
Claude Gazin
Sung Mi Park
Lihua J Zhu
Marie-anne Debily
Ellen L W Kittler
Maria L Zapp
David Lapointe
Stephane Gobeil
Ching-Man Virbasius
Michael R Green
A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.
PLoS Genetics
title A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.
title_full A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.
title_fullStr A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.
title_full_unstemmed A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.
title_short A synthetic interaction screen identifies factors selectively required for proliferation and TERT transcription in p53-deficient human cancer cells.
title_sort synthetic interaction screen identifies factors selectively required for proliferation and tert transcription in p53 deficient human cancer cells
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1003151&type=printable
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