PMID:16385024 - Revision history

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	'''~~No author listed~~''' (2006) Recruitment of Bacillus subtilis RecN to DNA double-strand breaks in the absence of DNA end processing. ''J. Bacteriol.'' '''188''':353-60		'''Sanchez, H, Kidane, D, Castillo Cozar, M, Graumann, PL and Alonso, JC''' (2006) Recruitment of Bacillus subtilis RecN to DNA double-strand breaks in the absence of DNA end processing. ''J. Bacteriol.'' '''188''':353-60
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 ==EcoliWiki Links {{HelpIcon|Help:Literature}} ==

imported>Wikientrybot: change PMID template to TableEdit version

2013-09-01T18:51:06Z

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	<~~protect~~>		<!--box uid=d41d8cd98f00b204e9800998ecf8427e.180950.B52238c9adbb11-->
	<~~span style = 'font~~-~~size: large'> '''Sanchez, H, Kidane, D, Castillo Cozar, M, Graumann, PL and Alonso, JC''~~' ~~(2006) Recruitment of Bacillus subtilis RecN to DNA double-strand breaks in~~ the ~~absence of DNA end processing~~.~~''J. Bacteriol.'' '''188''':353~~-~~60</span~~>		<!--
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	\|~~{{TableHeadingColor}}~~ \|'''~~Abstract~~''' ~~\|\| <protect>The recognition and processing~~ of double-strand breaks ~~(DSBs) to a 3' single-stranded DNA (ssDNA) overhang structure in Bacillus subtilis is poorly understood. Mutations~~ in ~~addA and addB or null mutations in recJ (DeltarecJ), recQ (DeltarecQ), or recS (DeltarecS) genes, when present in otherwise-Rec+ cells, render cells moderately sensitive to~~ the ~~killing action~~ of ~~different~~ DNA~~-damaging agents~~. Inactivation of a RecQ-like helicase (DeltarecQ or DeltarecS) in addAB cells showed an additive effect; however, when DeltarecJ was combined with addAB, a strong synergistic effect was observed with a survival rate similar to that of DeltarecA cells. ~~RecF was nonepistatic with RecJ or AddAB~~. After induction of DSBs, RecN-yellow fluorescent protein (YFP) foci were formed in addAB DeltarecJ cells. AddAB and RecJ were required for the formation of a single RecN focus, because in their absence multiple RecN-YFP foci accumulated within the cells. Green fluorescent protein-RecA failed to form filamentous structures (termed threads) in addAB DeltarecJ cells. We propose that RecN is one of the first recombination proteins detected as a discrete focus in live cells in response to DSBs and that either AddAB or RecQ(S)-RecJ are required for the generation of a duplex with a 3'-~~ssDNA tail needed for filament formation of RecA.</protect>~~		!align=left \|Citation
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			'''No author listed''' (2006) Recruitment of Bacillus subtilis RecN to DNA double-strand breaks in the absence of DNA end processing. ''J. Bacteriol.'' '''188''':353-60
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	\|~~{{TableHeadingColor}} nowrap~~ \|'''Links~~'''~~ \|\|		!align=left \|Abstract
	* [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16385024 PubMed]		\|\|
			The recognition and processing of double-strand breaks (DSBs) to a 3' single-stranded DNA (ssDNA) overhang structure in Bacillus subtilis is poorly understood. Mutations in addA and addB or null mutations in recJ (DeltarecJ), recQ (DeltarecQ), or recS (DeltarecS) genes, when present in otherwise-Rec+ cells, render cells moderately sensitive to the killing action of different DNA-damaging agents. Inactivation of a RecQ-like helicase (DeltarecQ or DeltarecS) in addAB cells showed an additive effect; however, when DeltarecJ was combined with addAB, a strong synergistic effect was observed with a survival rate similar to that of DeltarecA cells. RecF was nonepistatic with RecJ or AddAB. After induction of DSBs, RecN-yellow fluorescent protein (YFP) foci were formed in addAB DeltarecJ cells. AddAB and RecJ were required for the formation of a single RecN focus, because in their absence multiple RecN-YFP foci accumulated within the cells. Green fluorescent protein-RecA failed to form filamentous structures (termed threads) in addAB DeltarecJ cells. We propose that RecN is one of the first recombination proteins detected as a discrete focus in live cells in response to DSBs and that either AddAB or RecQ(S)-RecJ are required for the generation of a duplex with a 3'-ssDNA tail needed for filament formation of RecA.
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			[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16385024 PubMed] [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347269 PMC1347269]
	Online version:[http://dx.doi.org/10.1128/JB.188.2.353-360.2006 10.1128/JB.188.2.353-360.2006]		Online version:[http://dx.doi.org/10.1128/JB.188.2.353-360.2006 10.1128/JB.188.2.353-360.2006]
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			!align=left \|Keywords
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			3' Flanking Region; Bacillus subtilis/genetics; Bacterial Proteins/metabolism; Bacterial Proteins/physiology; DNA Repair; DNA Restriction Enzymes/physiology; DNA, Bacterial/genetics; DNA, Single-Stranded/genetics; DNA, Single-Stranded/metabolism; Exodeoxyribonucleases/metabolism; Rec A Recombinases/metabolism; Recombination, Genetic

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	==Significance {{HelpIcon\|Help:Literature}} ==		==Significance {{HelpIcon\|Help:Literature}} ==
	{{LitSignificance}}		{{LitSignificance}}

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2012-02-22T05:38:45Z

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		<span style = 'font-size: large'> '''Sanchez, H, Kidane, D, Castillo Cozar, M, Graumann, PL and Alonso, JC''' (2006) Recruitment of Bacillus subtilis RecN to DNA double-strand breaks in the absence of DNA end processing.''J. Bacteriol.'' '''188''':353-60</span>

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		\|{{TableHeadingColor}} \|'''Abstract''' \|\| <protect>The recognition and processing of double-strand breaks (DSBs) to a 3' single-stranded DNA (ssDNA) overhang structure in Bacillus subtilis is poorly understood. Mutations in addA and addB or null mutations in recJ (DeltarecJ), recQ (DeltarecQ), or recS (DeltarecS) genes, when present in otherwise-Rec+ cells, render cells moderately sensitive to the killing action of different DNA-damaging agents. Inactivation of a RecQ-like helicase (DeltarecQ or DeltarecS) in addAB cells showed an additive effect; however, when DeltarecJ was combined with addAB, a strong synergistic effect was observed with a survival rate similar to that of DeltarecA cells. RecF was nonepistatic with RecJ or AddAB. After induction of DSBs, RecN-yellow fluorescent protein (YFP) foci were formed in addAB DeltarecJ cells. AddAB and RecJ were required for the formation of a single RecN focus, because in their absence multiple RecN-YFP foci accumulated within the cells. Green fluorescent protein-RecA failed to form filamentous structures (termed threads) in addAB DeltarecJ cells. We propose that RecN is one of the first recombination proteins detected as a discrete focus in live cells in response to DSBs and that either AddAB or RecQ(S)-RecJ are required for the generation of a duplex with a 3'-ssDNA tail needed for filament formation of RecA.</protect>
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		* [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16385024 PubMed]
		Online version:[http://dx.doi.org/10.1128/JB.188.2.353-360.2006 10.1128/JB.188.2.353-360.2006]
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		==Significance {{HelpIcon\|Help:Literature}} ==
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		!\|Gene product!!Qualifier!!GO ID!!GO term name!!Evidence Code!!with/from!!Aspect!!Notes!!Status

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		==See also==

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