Msl2 is a novel component of the vertebrate DNA damage response (Q28534565)

1

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Simona Moravcová

2

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Yvan Canitrot

3

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Lukasz P Andrzejewski

4

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Dervla M Walshe

Creative Commons Attribution 4.0 International

5

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language of work or name

English

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publication date

2013

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published in

PLOS One

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volume

8

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issue

7

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page(s)

e68549

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copyright license

start time

9 July 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3706407/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Multiple facets of the DNA damage response contribute to the radioresistance of mouse mesenchymal stromal cell lines

29 September 2017

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The in vivo dynamic interplay of MDC1 and 53BP1 at DNA damage-induced nuclear foci.

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Bat3 facilitates H3K79 dimethylation by DOT1L and promotes DNA damage-induced 53BP1 foci at G1/G2 cell-cycle phases

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The RING finger protein MSL2 in the MOF complex is an E3 ubiquitin ligase for H2B K34 and is involved in crosstalk with H3 K4 and K79 methylation

29 September 2017

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Methylated H3K4, a Transcription-Associated Histone Modification, Is Involved in the DNA Damage Response Pathway

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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The right dose for every sex

29 September 2017

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DNA double-strand break repair: all's well that ends well

29 September 2017

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Nuclear pore components are involved in the transcriptional regulation of dosage compensation in Drosophila

29 September 2017

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The role of the non-homologous end-joining pathway in lymphocyte development

29 September 2017

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Genetic analysis of the DNA-dependent protein kinase reveals an inhibitory role of Ku in late S-G2 phase DNA double-strand break repair

29 September 2017

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Complex formation by the Drosophila MSL proteins: role of the MSL2 RING finger in protein complex assembly

29 September 2017

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Expression of msl-2 causes assembly of dosage compensation regulators on the X chromosomes and female lethality in Drosophila

29 September 2017

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MOF and H4 K16 acetylation play important roles in DNA damage repair by modulating recruitment of DNA damage repair protein Mdc1.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706407

Two mammalian MOF complexes regulate transcription activation by distinct mechanisms

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3706407

Di-methyl H4 lysine 20 targets the checkpoint protein Crb2 to sites of DNA damage

2 June 2018

1 reference

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The DNA polymerase lambda is required for the repair of non-compatible DNA double strand breaks by NHEJ in mammalian cells

2 June 2018

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The histone acetyltransferase hMOF is frequently downregulated in primary breast carcinoma and medulloblastoma and constitutes a biomarker for clinical outcome in medulloblastoma

2 June 2018

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Acetylation of the p53 DNA-binding domain regulates apoptosis induction

21 January 2018

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Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila.

21 January 2018

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MSL2 combines sensor and effector functions in homeostatic control of the Drosophila dosage compensation machinery.

21 January 2018

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The direct interaction between 53BP1 and MDC1 is required for the recruitment of 53BP1 to sites of damage

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PubMed

https://pubmed.ncbi.nlm.nih.gov/23874665