Histone H2AX is phosphorylated at sites of retroviral DNA integration but is dispensable for postintegration repair. (Q33205906)

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31 December 2019

title

Histone H2AX is phosphorylated at sites of retroviral DNA integration but is dispensable for postintegration repair (English)

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Anna Marie Skalka

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31 December 2019

author name string

Joseph Ramcharan

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Emmy Rogakou

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Konstantin D Taganov

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James G Greger

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William Bonner

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André Nussenzweig

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Richard A Katz

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language of work or name

English

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publication date

11 August 2004

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Journal of Biological Chemistry

31 December 2019

published in

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volume

279

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page(s)

45810-45814

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issue

44

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DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139

31 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

ATM phosphorylates histone H2AX in response to DNA double-strand breaks

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

Histone H2AX is phosphorylated in an ATR-dependent manner in response to replicational stress

21 January 2018

1 reference

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ATM and DNA-PK function redundantly to phosphorylate H2AX after exposure to ionizing radiation

21 January 2018

1 reference

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Megabase chromatin domains involved in DNA double-strand breaks in vivo

21 January 2018

1 reference

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Histone H2A variants H2AX and H2AZ

21 January 2018

1 reference

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Genomic instability in mice lacking histone H2AX

21 January 2018

1 reference

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Increased ionizing radiation sensitivity and genomic instability in the absence of histone H2AX

21 January 2018

1 reference

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Response to RAG-mediated VDJ cleavage by NBS1 and gamma-H2AX

21 January 2018

1 reference

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AID is required to initiate Nbs1/gamma-H2AX focus formation and mutations at sites of class switching

21 January 2018

1 reference

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Recombinational DNA double-strand breaks in mice precede synapsis

21 January 2018

1 reference

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H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis

21 January 2018

1 reference

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Kinetics of human immunodeficiency virus type 1 (HIV) DNA integration in acutely infected cells as determined using a novel assay for detection of integrated HIV DNA.

21 January 2018

1 reference

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21 January 2018

The retroviral enzymes

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21 January 2018

1 reference

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A role for DNA-PK in retroviral DNA integration

21 January 2018

1 reference

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Wortmannin potentiates integrase-mediated killing of lymphocytes and reduces the efficiency of stable transduction by retroviruses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

Evidence that the retroviral DNA integration process triggers an ATR-dependent DNA damage response

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

Evidence that stable retroviral transduction and cell survival following DNA integration depend on components of the nonhomologous end joining repair pathway

21 January 2018

1 reference

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Coexamination of site-specific transcription factor binding and promoter activity in living cells

21 January 2018

1 reference

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Human immunodeficiency virus type 1 DNA nuclear import and integration are mitosis independent in cycling cells

21 January 2018

1 reference

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Transduction of interphase cells by avian sarcoma virus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

Histone H2AX phosphorylation is dispensable for the initial recognition of DNA breaks

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

H2AX haploinsufficiency modifies genomic stability and tumor susceptibility

21 January 2018

1 reference

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A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage

21 January 2018

1 reference

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MDC1 is a mediator of the mammalian DNA damage checkpoint

21 January 2018

1 reference

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Accumulation of Checkpoint Protein 53BP1 at DNA Breaks Involves Its Binding to Phosphorylated Histone H2AX

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

DNA damage-induced G2-M checkpoint activation by histone H2AX and 53BP1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

H2AX is required for recombination between immunoglobulin switch regions but not for intra-switch region recombination or somatic hypermutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

H2AX may function as an anchor to hold broken chromosomal DNA ends in close proximity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

H2AX: the histone guardian of the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

Autoubiquitylation of the V(D)J recombinase protein RAG1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M407886200

21 January 2018

Identifiers

DOI

10.1074/JBC.M407886200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15308627%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

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