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PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1

LIMD1 is a tumour suppressor gene (TSG) down regulated in ∼80% of lung cancers with loss also demonstrated in breast and head and neck squamous cell carcinomas. LIMD1 is also a candidate TSG in childhood acute lymphoblastic leukaemia. Mechanistically, LIMD1 interacts with pRB, repressing E2F-driven...

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Autores principales: Foxler, Daniel E., James, Victoria, Shelton, Samuel J., Vallim, Thomas Q. de A., Shaw, Peter E., Sharp, Tyson V.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078326/
https://www.ncbi.nlm.nih.gov/pubmed/21402070
http://dx.doi.org/10.1016/j.febslet.2011.03.013
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author Foxler, Daniel E.
James, Victoria
Shelton, Samuel J.
Vallim, Thomas Q. de A.
Shaw, Peter E.
Sharp, Tyson V.
author_facet Foxler, Daniel E.
James, Victoria
Shelton, Samuel J.
Vallim, Thomas Q. de A.
Shaw, Peter E.
Sharp, Tyson V.
author_sort Foxler, Daniel E.
collection PubMed
description LIMD1 is a tumour suppressor gene (TSG) down regulated in ∼80% of lung cancers with loss also demonstrated in breast and head and neck squamous cell carcinomas. LIMD1 is also a candidate TSG in childhood acute lymphoblastic leukaemia. Mechanistically, LIMD1 interacts with pRB, repressing E2F-driven transcription as well as being a critical component of microRNA-mediated gene silencing. In this study we show a CpG island within the LIMD1 promoter contains a conserved binding motif for the transcription factor PU.1. Mutation of the PU.1 consensus reduced promoter driven transcription by 90%. ChIP and EMSA analysis demonstrated that PU.1 specifically binds to the LIMD1 promoter. siRNA depletion of PU.1 significantly reduced endogenous LIMD1 expression, demonstrating that PU.1 is a major transcriptional activator of LIMD1.
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spelling pubmed-30783262011-05-03 PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1 Foxler, Daniel E. James, Victoria Shelton, Samuel J. Vallim, Thomas Q. de A. Shaw, Peter E. Sharp, Tyson V. FEBS Lett Article LIMD1 is a tumour suppressor gene (TSG) down regulated in ∼80% of lung cancers with loss also demonstrated in breast and head and neck squamous cell carcinomas. LIMD1 is also a candidate TSG in childhood acute lymphoblastic leukaemia. Mechanistically, LIMD1 interacts with pRB, repressing E2F-driven transcription as well as being a critical component of microRNA-mediated gene silencing. In this study we show a CpG island within the LIMD1 promoter contains a conserved binding motif for the transcription factor PU.1. Mutation of the PU.1 consensus reduced promoter driven transcription by 90%. ChIP and EMSA analysis demonstrated that PU.1 specifically binds to the LIMD1 promoter. siRNA depletion of PU.1 significantly reduced endogenous LIMD1 expression, demonstrating that PU.1 is a major transcriptional activator of LIMD1. Elsevier Science B.V 2011-04-06 /pmc/articles/PMC3078326/ /pubmed/21402070 http://dx.doi.org/10.1016/j.febslet.2011.03.013 Text en © 2011 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Foxler, Daniel E.
James, Victoria
Shelton, Samuel J.
Vallim, Thomas Q. de A.
Shaw, Peter E.
Sharp, Tyson V.
PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1
title PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1
title_full PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1
title_fullStr PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1
title_full_unstemmed PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1
title_short PU.1 is a major transcriptional activator of the tumour suppressor gene LIMD1
title_sort pu.1 is a major transcriptional activator of the tumour suppressor gene limd1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078326/
https://www.ncbi.nlm.nih.gov/pubmed/21402070
http://dx.doi.org/10.1016/j.febslet.2011.03.013
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