53BP1 represses mitotic catastrophe in syncytia elicited by the HIV-1 envelope. (Q48421018)

11 February 2018

title

53BP1 represses mitotic catastrophe in syncytia elicited by the HIV-1 envelope. (English)

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15

G Kroemer

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14

M Piacentini

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author name string

J-L Perfettini

1

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R Nardacci

2

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C Séror

3

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S Q Raza

4

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S Sepe

5

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H Saïdi

6

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F Brottes

7

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A Amendola

8

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F Subra

9

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F Del Nonno

10

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L Chessa

11

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A D'Incecco

12

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M-L Gougeon

13

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publication date

30 October 2009

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Cell Death & Differentiation

published in

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volume

17

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issue

5

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page(s)

811-820

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https://scigraph.springernature.com/pub.10.1038/cdd.2009.159

exact match

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cites work

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NF-kappaB and p53 are the dominant apoptosis-inducing transcription factors elicited by the HIV-1 envelope

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Site-specific Mutations in HIV-1 gp41 Reveal a Correlation between HIV-1-mediated Bystander Apoptosis and Fusion/Hemifusion

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Role of HIV Gp41 mediated fusion/hemifusion in bystander apoptosis

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Human immunodeficiency virus 1 envelope glycoprotein complex-induced apoptosis involves mammalian target of rapamycin/FKBP12-rapamycin-associated protein-mediated p53 phosphorylation

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Sequential involvement of Cdk1, mTOR and p53 in apoptosis induced by the HIV-1 envelope

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Essential role of p53 phosphorylation by p38 MAPK in apoptosis induction by the HIV-1 envelope

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Critical involvement of the ATM-dependent DNA damage response in the apoptotic demise of HIV-1-elicited syncytia

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Pro-apoptotic function of checkpoint kinase-2 in syncytia elicited by the HIV-1 envelope.

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p53-A pro-apoptotic signal transducer involved in AIDS

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Apoptosis control in syncytia induced by the HIV type 1-envelope glycoprotein complex: role of mitochondria and caspases.

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The tumor suppressor protein PML controls apoptosis induced by the HIV-1 envelope.

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53BP1, a mediator of the DNA damage checkpoint

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Tumor suppressor p53 binding protein 1 (53BP1) is involved in DNA damage-signaling pathways

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p53 Binding protein 53BP1 is required for DNA damage responses and tumor suppression in mice

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53BP1 facilitates long-range DNA end-joining during V(D)J recombination

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53BP1 promotes non-homologous end joining of telomeres by increasing chromatin mobility

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

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An oligomerized 53BP1 tudor domain suffices for recognition of DNA double-strand breaks

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p53 binding protein 1 (53BP1) is an early participant in the cellular response to DNA double-strand breaks

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Potential role for 53BP1 in DNA end-joining repair through direct interaction with DNA.

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Phosphorylation and rapid relocalization of 53BP1 to nuclear foci upon DNA damage

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53BP1 functions in an ATM-dependent checkpoint pathway that is constitutively activated in human cancer

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Protein phosphatase 5 regulates the function of 53BP1 after neocarzinostatin-induced DNA damage

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Negative cell cycle regulation and DNA damage-inducible phosphorylation of the BRCT protein 53BP1.

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Characterisation of the sites of DNA damage-induced 53BP1 phosphorylation catalysed by ATM and ATR.

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Retroviral DNA integration and the DNA damage response

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Activation of the ATR pathway by human immunodeficiency virus type 1 Vpr involves its direct binding to chromatin in vivo

21 January 2018

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Cell death by mitotic catastrophe: a molecular definition

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21 January 2018

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RNF8-dependent and RNF8-independent regulation of 53BP1 in response to DNA damage

21 January 2018

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Mitochondrion-dependent caspase activation by the HIV-1 envelope

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Apoptosis and karyogamy in syncytia induced by the HIV-1-envelope glycoprotein complex

1 reference

https://api.crossref.org/works/10.1038%2FCDD.2009.159

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/CDD.2009.159

1 reference

11 February 2018

Dimensions Publication ID

0 references

1 reference

11 February 2018