id ir-10336-23864
recordtype dspace
spelling ir-10336-238642022-05-02T12:37:17Z BACH2: A marker of DNA damage and ageing Uittenboogaard, L.M. Payan-Gomez, Cesar Pothof, J. van IJcken, W. Mastroberardino, P.G. van der Pluijm, I. Hoeijmakers, J.H.J. Tresini, M. Biological marker Messenger rna Protein v maf Transcription factor Transcription factor bach2 Unclassified drug Aging Animal experiment Animal tissue Article Dna damage Down regulation Excision repair Gene expression profiling Gene identification Genetic association Human Human cell Immune system Microarray analysis Mouse Nonhuman Priority journal Protein expression Transcription regulation Ultraviolet radiation Murinae Mus Ageing Bach2 Dna damage Meta-analysis Nrf2 Aging Animals Basic-leucine zipper transcription factors Biological markers Cell survival Dna damage Gene expression regulation Hek293 cells Humans Mice Nih 3t3 cells Oligonucleotide array sequence analysis Ultraviolet rays Ageing Bach2 Dna damage Meta-analysis Nrf2 ionizing animal Models Radiation DNA damage and ageing share expression changes involving alterations in many aspects of metabolism, suppression of growth and upregulation of defence and genome maintenance systems. 'Omics' technologies have permitted large-scale parallel measurements covering global cellular constituents and aided the identification of specific response pathways that change during ageing and after DNA damage. We have set out to identify genes with highly conserved response patterns through meta-analysis of mRNA expression datasets collected during natural ageing and accelerated ageing caused by a Transcription-Coupled Nucleotide Excision Repair (TC-NER) defect in a diverse set of organs and tissues in mice, and from in vitro UV-induced DNA damage in a variety of murine cells. The identified set of genes that show similar expression patterns in response to organ ageing (accelerated and normal), and endogenously and exogenously induced DNA damage, consists of genes involved in anti-oxidant systems and includes the transcription factor Bach2 as one of the most consistent markers. BACH2 was originally identified as a partner of the small Maf proteins and antagonist of the NRF2 anti-oxidant defence pathway and has been implicated in B-cell differentiation and immune system homeostasis. Although BACH2 has never before been associated with UV-induced damage or ageing, it shows a strong downregulation in both conditions. We have characterized the dynamics of Bach2 expression in response to DNA damage and show that it is a highly sensitive responder to transcription-blocking DNA lesions. Gene expression profiling using Affymetrix microarray analysis after siRNA-mediated silencing of Bach2 identified cell cycle and transcription regulation as the most significantly altered processes consistent with a function as transcription factor affecting proliferation. © 2013 Elsevier B.V. 2013 2020-05-26T00:06:11Z info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 15687864 https://repository.urosario.edu.co/handle/10336/23864 https://doi.org/10.1016/j.dnarep.2013.08.016 eng info:eu-repo/semantics/openAccess application/pdf instname:Universidad del Rosario
institution EdocUR - Universidad del Rosario
collection DSpace
language Inglés (English)
topic Biological marker
Messenger rna
Protein v maf
Transcription factor
Transcription factor bach2
Unclassified drug
Aging
Animal experiment
Animal tissue
Article
Dna damage
Down regulation
Excision repair
Gene expression profiling
Gene identification
Genetic association
Human
Human cell
Immune system
Microarray analysis
Mouse
Nonhuman
Priority journal
Protein expression
Transcription regulation
Ultraviolet radiation
Murinae
Mus
Ageing
Bach2
Dna damage
Meta-analysis
Nrf2
Aging
Animals
Basic-leucine zipper transcription factors
Biological markers
Cell survival
Dna damage
Gene expression regulation
Hek293 cells
Humans
Mice
Nih 3t3 cells
Oligonucleotide array sequence analysis
Ultraviolet rays
Ageing
Bach2
Dna damage
Meta-analysis
Nrf2
ionizing
animal
Models
Radiation
spellingShingle Biological marker
Messenger rna
Protein v maf
Transcription factor
Transcription factor bach2
Unclassified drug
Aging
Animal experiment
Animal tissue
Article
Dna damage
Down regulation
Excision repair
Gene expression profiling
Gene identification
Genetic association
Human
Human cell
Immune system
Microarray analysis
Mouse
Nonhuman
Priority journal
Protein expression
Transcription regulation
Ultraviolet radiation
Murinae
Mus
Ageing
Bach2
Dna damage
Meta-analysis
Nrf2
Aging
Animals
Basic-leucine zipper transcription factors
Biological markers
Cell survival
Dna damage
Gene expression regulation
Hek293 cells
Humans
Mice
Nih 3t3 cells
Oligonucleotide array sequence analysis
Ultraviolet rays
Ageing
Bach2
Dna damage
Meta-analysis
Nrf2
ionizing
animal
Models
Radiation
Uittenboogaard, L.M.
Payan-Gomez, Cesar
Pothof, J.
van IJcken, W.
Mastroberardino, P.G.
van der Pluijm, I.
Hoeijmakers, J.H.J.
Tresini, M.
BACH2: A marker of DNA damage and ageing
description DNA damage and ageing share expression changes involving alterations in many aspects of metabolism, suppression of growth and upregulation of defence and genome maintenance systems. 'Omics' technologies have permitted large-scale parallel measurements covering global cellular constituents and aided the identification of specific response pathways that change during ageing and after DNA damage. We have set out to identify genes with highly conserved response patterns through meta-analysis of mRNA expression datasets collected during natural ageing and accelerated ageing caused by a Transcription-Coupled Nucleotide Excision Repair (TC-NER) defect in a diverse set of organs and tissues in mice, and from in vitro UV-induced DNA damage in a variety of murine cells. The identified set of genes that show similar expression patterns in response to organ ageing (accelerated and normal), and endogenously and exogenously induced DNA damage, consists of genes involved in anti-oxidant systems and includes the transcription factor Bach2 as one of the most consistent markers. BACH2 was originally identified as a partner of the small Maf proteins and antagonist of the NRF2 anti-oxidant defence pathway and has been implicated in B-cell differentiation and immune system homeostasis. Although BACH2 has never before been associated with UV-induced damage or ageing, it shows a strong downregulation in both conditions. We have characterized the dynamics of Bach2 expression in response to DNA damage and show that it is a highly sensitive responder to transcription-blocking DNA lesions. Gene expression profiling using Affymetrix microarray analysis after siRNA-mediated silencing of Bach2 identified cell cycle and transcription regulation as the most significantly altered processes consistent with a function as transcription factor affecting proliferation. © 2013 Elsevier B.V.
format Artículo (Article)
author Uittenboogaard, L.M.
Payan-Gomez, Cesar
Pothof, J.
van IJcken, W.
Mastroberardino, P.G.
van der Pluijm, I.
Hoeijmakers, J.H.J.
Tresini, M.
author_facet Uittenboogaard, L.M.
Payan-Gomez, Cesar
Pothof, J.
van IJcken, W.
Mastroberardino, P.G.
van der Pluijm, I.
Hoeijmakers, J.H.J.
Tresini, M.
author_sort Uittenboogaard, L.M.
title BACH2: A marker of DNA damage and ageing
title_short BACH2: A marker of DNA damage and ageing
title_full BACH2: A marker of DNA damage and ageing
title_fullStr BACH2: A marker of DNA damage and ageing
title_full_unstemmed BACH2: A marker of DNA damage and ageing
title_sort bach2: a marker of dna damage and ageing
publishDate 2013
url https://repository.urosario.edu.co/handle/10336/23864
https://doi.org/10.1016/j.dnarep.2013.08.016
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score 12,131701