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Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs

Artemis is an endonuclease that opens coding hairpin ends during V(D)J recombination and has critical roles in postirradiation cell survival. A direct role for the C-terminal region of Artemis in V(D)J recombination has not been defined, despite the presence of immunodeficiency and lymphoma developm...

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Autores principales: Malu, Shruti, De Ioannes, Pablo, Kozlov, Mikhail, Greene, Marsha, Francis, Dailia, Hanna, Mary, Pena, Jesse, Escalante, Carlos R., Kurosawa, Aya, Erdjument-Bromage, Hediye, Tempst, Paul, Adachi, Noritaka, Vezzoni, Paolo, Villa, Anna, Aggarwal, Aneel K., Cortes, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348108/
https://www.ncbi.nlm.nih.gov/pubmed/22529269
http://dx.doi.org/10.1084/jem.20111437
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author Malu, Shruti
De Ioannes, Pablo
Kozlov, Mikhail
Greene, Marsha
Francis, Dailia
Hanna, Mary
Pena, Jesse
Escalante, Carlos R.
Kurosawa, Aya
Erdjument-Bromage, Hediye
Tempst, Paul
Adachi, Noritaka
Vezzoni, Paolo
Villa, Anna
Aggarwal, Aneel K.
Cortes, Patricia
author_facet Malu, Shruti
De Ioannes, Pablo
Kozlov, Mikhail
Greene, Marsha
Francis, Dailia
Hanna, Mary
Pena, Jesse
Escalante, Carlos R.
Kurosawa, Aya
Erdjument-Bromage, Hediye
Tempst, Paul
Adachi, Noritaka
Vezzoni, Paolo
Villa, Anna
Aggarwal, Aneel K.
Cortes, Patricia
author_sort Malu, Shruti
collection PubMed
description Artemis is an endonuclease that opens coding hairpin ends during V(D)J recombination and has critical roles in postirradiation cell survival. A direct role for the C-terminal region of Artemis in V(D)J recombination has not been defined, despite the presence of immunodeficiency and lymphoma development in patients with deletions in this region. Here, we report that the Artemis C-terminal region directly interacts with the DNA-binding domain of Ligase IV, a DNA Ligase which plays essential roles in DNA repair and V(D)J recombination. The Artemis–Ligase IV interaction is specific and occurs independently of the presence of DNA and DNA–protein kinase catalytic subunit (DNA-PKcs), another protein known to interact with the Artemis C-terminal region. Point mutations in Artemis that disrupt its interaction with Ligase IV or DNA-PKcs reduce V(D)J recombination, and Artemis mutations that affect interactions with Ligase IV and DNA-PKcs show additive detrimental effects on coding joint formation. Signal joint formation remains unaffected. Our data reveal that the C-terminal region of Artemis influences V(D)J recombination through its interaction with both Ligase IV and DNA-PKcs.
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spelling pubmed-33481082012-11-07 Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs Malu, Shruti De Ioannes, Pablo Kozlov, Mikhail Greene, Marsha Francis, Dailia Hanna, Mary Pena, Jesse Escalante, Carlos R. Kurosawa, Aya Erdjument-Bromage, Hediye Tempst, Paul Adachi, Noritaka Vezzoni, Paolo Villa, Anna Aggarwal, Aneel K. Cortes, Patricia J Exp Med Brief Definitive Report Artemis is an endonuclease that opens coding hairpin ends during V(D)J recombination and has critical roles in postirradiation cell survival. A direct role for the C-terminal region of Artemis in V(D)J recombination has not been defined, despite the presence of immunodeficiency and lymphoma development in patients with deletions in this region. Here, we report that the Artemis C-terminal region directly interacts with the DNA-binding domain of Ligase IV, a DNA Ligase which plays essential roles in DNA repair and V(D)J recombination. The Artemis–Ligase IV interaction is specific and occurs independently of the presence of DNA and DNA–protein kinase catalytic subunit (DNA-PKcs), another protein known to interact with the Artemis C-terminal region. Point mutations in Artemis that disrupt its interaction with Ligase IV or DNA-PKcs reduce V(D)J recombination, and Artemis mutations that affect interactions with Ligase IV and DNA-PKcs show additive detrimental effects on coding joint formation. Signal joint formation remains unaffected. Our data reveal that the C-terminal region of Artemis influences V(D)J recombination through its interaction with both Ligase IV and DNA-PKcs. The Rockefeller University Press 2012-05-07 /pmc/articles/PMC3348108/ /pubmed/22529269 http://dx.doi.org/10.1084/jem.20111437 Text en © 2012 Malu et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Brief Definitive Report
Malu, Shruti
De Ioannes, Pablo
Kozlov, Mikhail
Greene, Marsha
Francis, Dailia
Hanna, Mary
Pena, Jesse
Escalante, Carlos R.
Kurosawa, Aya
Erdjument-Bromage, Hediye
Tempst, Paul
Adachi, Noritaka
Vezzoni, Paolo
Villa, Anna
Aggarwal, Aneel K.
Cortes, Patricia
Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs
title Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs
title_full Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs
title_fullStr Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs
title_full_unstemmed Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs
title_short Artemis C-terminal region facilitates V(D)J recombination through its interactions with DNA Ligase IV and DNA-PKcs
title_sort artemis c-terminal region facilitates v(d)j recombination through its interactions with dna ligase iv and dna-pkcs
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348108/
https://www.ncbi.nlm.nih.gov/pubmed/22529269
http://dx.doi.org/10.1084/jem.20111437
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