Extra View: Sirt1 Acts As A Gatekeeper Of Replication Initiation To Preserve Genomic Stability

Since the discovery of a yeast gene silencing modifier (Silent Information Modifier 2, SIR2) and its role in maintaining genomic stability more than two decades ago, SIR2 homologs (sirtuins) were identified in diverse species. Sirtuins are protein deacetylases that play diverse roles in proper cellu...

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Vydáno v:Nucleus Ročník 9; číslo 1; s. 307 - 313
Hlavní autoři: Utani, Koichi, Aladjem, Mirit I.
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States Taylor & Francis 01.01.2018
Informa UK Limited
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ISSN:1949-1034, 1949-1042, 1949-1042
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Abstract Since the discovery of a yeast gene silencing modifier (Silent Information Modifier 2, SIR2) and its role in maintaining genomic stability more than two decades ago, SIR2 homologs (sirtuins) were identified in diverse species. Sirtuins are protein deacetylases that play diverse roles in proper cellular metabolism including cell cycle progression and maintenance of genomic stability. In yeast, SIR2 interacts with replication origins and protein complexes that affect both replication origin usage and gene silencing. In metazoans, the largest SIR2 homolog, SIRT1, is implicated in epigenetic modifications, circadian signaling, DNA recombination and DNA repair. Until recently, very few studies investigated the role of mammalian SIRT1 in modulating DNA replication. We discuss a newly characterized interaction between human SIRT1 and the DNA replication machinery, reviewing data from recent studies that have investigated how complex signaling pathways that involve SIRT1 affect cellular growth regulatory circuits.
AbstractList Since the discovery of a yeast gene silencing modifier (Silent Information Modifier 2, SIR2) and its role in maintaining genomic stability more than two decades ago, SIR2 homologs (sirtuins) were identified in diverse species. Sirtuins are protein deacetylases that play diverse roles in proper cellular metabolism including cell cycle progression and maintenance of genomic stability. In yeast, SIR2 interacts with replication origins and protein complexes that affect both replication origin usage and gene silencing. In metazoans, the largest SIR2 homolog, SIRT1, is implicated in epigenetic modifications, circadian signaling, DNA recombination and DNA repair. Until recently, very few studies investigated the role of mammalian SIRT1 in modulating DNA replication. We discuss a newly characterized interaction between human SIRT1 and the DNA replication machinery, reviewing data from recent studies that have investigated how complex signaling pathways that involve SIRT1 affect cellular growth regulatory circuits.
Since the discovery of a yeast gene silencing modifier (Silent Information Modifier 2, SIR2) and its role in maintaining genomic stability more than two decades ago, SIR2 homologs (sirtuins) were identified in diverse species. Sirtuins are protein deacetylases that play diverse roles in proper cellular metabolism including cell cycle progression and maintenance of genomic stability. In yeast, SIR2 interacts with replication origins and protein complexes that affect both replication origin usage and gene silencing. In metazoans, the largest SIR2 homolog, SIRT1, is implicated in epigenetic modifications, circadian signaling, DNA recombination and DNA repair. Until recently, very few studies investigated the role of mammalian SIRT1 in modulating DNA replication. We discuss a newly characterized interaction between human SIRT1 and the DNA replication machinery, reviewing data from recent studies that have investigated how complex signaling pathways that involve SIRT1 affect cellular growth regulatory circuits.Since the discovery of a yeast gene silencing modifier (Silent Information Modifier 2, SIR2) and its role in maintaining genomic stability more than two decades ago, SIR2 homologs (sirtuins) were identified in diverse species. Sirtuins are protein deacetylases that play diverse roles in proper cellular metabolism including cell cycle progression and maintenance of genomic stability. In yeast, SIR2 interacts with replication origins and protein complexes that affect both replication origin usage and gene silencing. In metazoans, the largest SIR2 homolog, SIRT1, is implicated in epigenetic modifications, circadian signaling, DNA recombination and DNA repair. Until recently, very few studies investigated the role of mammalian SIRT1 in modulating DNA replication. We discuss a newly characterized interaction between human SIRT1 and the DNA replication machinery, reviewing data from recent studies that have investigated how complex signaling pathways that involve SIRT1 affect cellular growth regulatory circuits.
Author Utani, Koichi
Aladjem, Mirit I.
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Cites_doi 10.1126/science.aao3172
10.1093/nar/gkp1039
10.1016/j.cell.2008.07.002
10.1073/pnas.1222494110
10.1038/sj.emboj.7600244
10.1038/nrm3293
10.1016/0092-8674(87)90642-8
10.1074/jbc.M113.520403
10.1172/JCI60818
10.1097/MOH.0000000000000152
10.1242/jcs.001222
10.1371/journal.ppat.1001080
10.1074/jbc.M115.641522
10.1093/nar/gkw322
10.1126/science.1140735
10.1529/biophysj.104.040824
10.1073/pnas.1010377108
10.1073/pnas.1010627107
10.1101/gad.228536.113
10.1038/ncomms8505
10.1038/ncb1848
10.1038/emboj.2011.404
10.1186/2041-9414-4-6
10.1093/nar/gkt131
10.1038/nsmb.2470
10.1016/S0092-8674(01)00524-4
10.1016/j.molcel.2016.09.017
10.1128/MCB.25.8.3109-3116.2005
10.1128/MCB.22.12.4136-4146.2002
10.1016/j.bcp.2014.08.034
10.1128/JVI.00102-17
10.1038/emm.2007.2
10.1371/journal.ppat.1005181
10.1016/j.molcel.2010.07.006
10.1016/j.molcel.2008.02.019
10.1038/nsmb.2543
10.1016/j.cell.2005.01.029
10.1074/mcp.M112.019547
10.1038/ncomms9548
10.7150/ijbs.11066
10.1126/science.1063957
10.1093/nar/gkx468
10.1016/j.molcel.2007.05.029
10.1016/j.molcel.2014.10.007
10.1016/j.molcel.2013.10.029
10.1016/j.ccr.2008.09.001
10.1016/j.cub.2015.09.026
10.1016/S0092-8674(00)80493-6
10.1038/ncomms11748
10.1016/S0092-8674(01)00527-X
10.1016/j.cub.2016.12.047
10.1128/JVI.77.3.2063-2070.2003
10.1016/j.ceb.2016.03.017
10.1074/jbc.M606774200
10.1016/j.cell.2008.10.025
10.1101/gad.9.23.2888
10.1038/nrg.2016.141
10.1038/s41598-017-04847-7
10.1074/jbc.M113.511337
10.1128/JVI.00219-14
10.1038/nrg.2017.46
10.1126/scisignal.aai8026
10.1371/journal.pone.0008414
10.1074/jbc.M709707200
10.1093/nar/gkv1019
10.1016/0092-8674(89)90681-8
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– notice: This work was authored as part of the Contributor's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law. 2018 This work was authored as part of the Contributor's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
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Issue 1
Keywords Epigenetics
Chromosome
Chromatin
DNA replication
Cell cycle
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References_xml – ident: CIT0022
  doi: 10.1126/science.aao3172
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  doi: 10.1093/nar/gkp1039
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  doi: 10.1016/j.cell.2008.07.002
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  doi: 10.1073/pnas.1222494110
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  doi: 10.1038/sj.emboj.7600244
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  doi: 10.1038/nrm3293
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  doi: 10.1016/0092-8674(87)90642-8
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  doi: 10.1074/jbc.M113.520403
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  doi: 10.1172/JCI60818
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  doi: 10.1097/MOH.0000000000000152
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  doi: 10.1242/jcs.001222
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  doi: 10.1371/journal.ppat.1001080
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  doi: 10.1074/jbc.M115.641522
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  doi: 10.1093/nar/gkw322
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  doi: 10.1126/science.1140735
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  doi: 10.1529/biophysj.104.040824
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  doi: 10.1073/pnas.1010377108
– ident: CIT0058
  doi: 10.1073/pnas.1010627107
– ident: CIT0016
  doi: 10.1101/gad.228536.113
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  doi: 10.1038/ncomms8505
– ident: CIT0059
  doi: 10.1038/ncb1848
– ident: CIT0054
  doi: 10.1038/emboj.2011.404
– ident: CIT0019
  doi: 10.1186/2041-9414-4-6
– ident: CIT0040
  doi: 10.1093/nar/gkt131
– ident: CIT0013
  doi: 10.1038/nsmb.2470
– ident: CIT0030
  doi: 10.1016/S0092-8674(01)00524-4
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  doi: 10.1016/j.molcel.2016.09.017
– ident: CIT0021
  doi: 10.1128/MCB.25.8.3109-3116.2005
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  doi: 10.1128/MCB.22.12.4136-4146.2002
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  doi: 10.1016/j.bcp.2014.08.034
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  doi: 10.1128/JVI.00102-17
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  doi: 10.1038/emm.2007.2
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  doi: 10.1371/journal.ppat.1005181
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  doi: 10.1016/j.molcel.2010.07.006
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  doi: 10.1016/j.molcel.2008.02.019
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  doi: 10.1038/nsmb.2543
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  doi: 10.1016/j.cell.2005.01.029
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  doi: 10.1074/mcp.M112.019547
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  doi: 10.1038/ncomms9548
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  doi: 10.7150/ijbs.11066
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  doi: 10.1126/science.1063957
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  doi: 10.1093/nar/gkx468
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Snippet Since the discovery of a yeast gene silencing modifier (Silent Information Modifier 2, SIR2) and its role in maintaining genomic stability more than two...
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SubjectTerms Animalia
Animals
Cell cycle
cell growth
Chromatin
Chromosome
DNA
DNA - genetics
DNA repair
DNA Replication
DNA Replication - genetics
Epigenetics
Extra View
genes
Genomic Instability
genomics
Humans
metabolism
replication origin
Silent Information Regulator Proteins, Saccharomyces cerevisiae
Silent Information Regulator Proteins, Saccharomyces cerevisiae - metabolism
Sirtuin 1
Sirtuin 1 - metabolism
Sirtuin 2
Sirtuin 2 - metabolism
sirtuins
yeasts
Title Extra View: Sirt1 Acts As A Gatekeeper Of Replication Initiation To Preserve Genomic Stability
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