"Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.

The recent revelation that there are small, noncoding RNAs that regulate the expression of many other genes has led to an exciting, emerging body of literature defining the biological role for these molecules within signaling networks. In a flurry of recent papers, a microRNA polycistron induced by...

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Main Authors: Hilary A Coller, Joshua J Forman, Aster Legesse-Miller
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-08-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC1959363?pdf=render
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spelling doaj-25ff61a43e5647539cbdfa01201fa5d62020-11-24T21:41:39ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042007-08-0138e14610.1371/journal.pgen.0030146"Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.Hilary A CollerJoshua J FormanAster Legesse-MillerThe recent revelation that there are small, noncoding RNAs that regulate the expression of many other genes has led to an exciting, emerging body of literature defining the biological role for these molecules within signaling networks. In a flurry of recent papers, a microRNA polycistron induced by the oncogenic transcription factor c-myc has been found to be involved in an unusually structured network of interactions. This network includes the seemingly paradoxical transcriptional induction and translational inhibition of the same molecule, the E2F1 transcription factor. This microRNA cluster has been implicated in inhibiting proliferation, as well as inhibiting apoptosis, and promoting angiogenesis. Consistent with its seemingly paradoxical functions, the region of the genome in which it is encoded is deleted in some tumors and overexpressed in others. We consider the possibility that members of this polycistronic microRNA cluster help cells to integrate signals from the environment and decide whether a signal should be interpreted as proliferative or apoptotic.http://europepmc.org/articles/PMC1959363?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Hilary A Coller
Joshua J Forman
Aster Legesse-Miller
spellingShingle Hilary A Coller
Joshua J Forman
Aster Legesse-Miller
"Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.
PLoS Genetics
author_facet Hilary A Coller
Joshua J Forman
Aster Legesse-Miller
author_sort Hilary A Coller
title "Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.
title_short "Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.
title_full "Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.
title_fullStr "Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.
title_full_unstemmed "Myc'ed messages": myc induces transcription of E2F1 while inhibiting its translation via a microRNA polycistron.
title_sort "myc'ed messages": myc induces transcription of e2f1 while inhibiting its translation via a microrna polycistron.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2007-08-01
description The recent revelation that there are small, noncoding RNAs that regulate the expression of many other genes has led to an exciting, emerging body of literature defining the biological role for these molecules within signaling networks. In a flurry of recent papers, a microRNA polycistron induced by the oncogenic transcription factor c-myc has been found to be involved in an unusually structured network of interactions. This network includes the seemingly paradoxical transcriptional induction and translational inhibition of the same molecule, the E2F1 transcription factor. This microRNA cluster has been implicated in inhibiting proliferation, as well as inhibiting apoptosis, and promoting angiogenesis. Consistent with its seemingly paradoxical functions, the region of the genome in which it is encoded is deleted in some tumors and overexpressed in others. We consider the possibility that members of this polycistronic microRNA cluster help cells to integrate signals from the environment and decide whether a signal should be interpreted as proliferative or apoptotic.
url http://europepmc.org/articles/PMC1959363?pdf=render
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