Heregulin, a new interactor of the telosome/shelterin complex in human telomeres

Autores
Menendez, Javier A.; Benboudjema, Louisa; Vellón, Luciano; Rubio, Miguel A.; Espinoza, Ingrid; Campisi, Judith; Lupu, Ruth
Año de publicación
2015
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Telomere length, shape and function depend on a complex of six core telomere-associated proteins referred to as the telosome or shelterin complex. We here demonstrate that the isoform beta2 of the heregulin family of growth factors (HRGbeta2) is a novel interactor of the telosome/shelterin complex in human telomeres. Analysis of protein-protein interactions using a high-throughput yeast two-hybrid (Y2H) screen identified RAP1, the only telomere protein that is conserved from yeasts to mammals, as a novel interacting partner of HRGbeta2. Deletion analysis of RAP1 revealed that the linker domain, a region previously suggested to recruit negative regulators of telomere length, interacts specifically with HRGbeta2. Co-immunoprecipitation and imaging experiments demonstrated that, in addition to RAP1, HRGβ2 could associate with the RAP1-associated telomeric repeat binding factor 2 (TRF2). Deletion analysis of HRGβ2 confirmed that a putative nuclear localization signal (NLS) was necessary for nuclear HRGbeta2 to exert a negative regulation of telomere length whereas the N-terminus (extracellular) amino acids of HRGbeta2 were sufficient to interact with RAP1/TRF2 and promote telomere shortening. Taken together, our studies identify nuclear HRGbeta2 as one of the previously unknown regulators predicted to be recruited by the RAP1 linker domain to negatively regulate telomere length in human cells. Our current findings reveal that a new, but likely not the last, unexpected visitor has arrived to the "telosome/shelterin town".
Fil: Menendez, Javier A.. Catalan Institute of Oncology; España. Girona Biomedical Research Institute; España
Fil: Benboudjema, Louisa. Evanston Northwestern Healthcare Research Institute; Estados Unidos
Fil: Vellón, Luciano. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental (i); Argentina
Fil: Rubio, Miguel A.. Hospital de la Santa Creu i Sant Pau. Institut d’Investigació Biomèdica Sant Pau,; España
Fil: Espinoza, Ingrid. University Of Mississippi; Estados Unidos. Lawrence Berkeley National Laboratory; Estados Unidos
Fil: Campisi, Judith. Lawrence Berkeley National Laboratory; Estados Unidos. Buck Institute for Research on Aging; Estados Unidos
Fil: Lupu, Ruth. Mayo Clinic Cancer Center; Estados Unidos. Mayo Clinic. Department of Laboratory Medicine and Pathology; Estados Unidos
Materia
TRF2
HEREGULIN
SHELTERING COMPLEX
TELOMERE
TELOSOME
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/7739

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network_acronym_str CONICETDig
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network_name_str CONICET Digital (CONICET)
spelling Heregulin, a new interactor of the telosome/shelterin complex in human telomeresMenendez, Javier A.Benboudjema, LouisaVellón, LucianoRubio, Miguel A.Espinoza, IngridCampisi, JudithLupu, RuthTRF2HEREGULINSHELTERING COMPLEXTELOMERETELOSOMEhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Telomere length, shape and function depend on a complex of six core telomere-associated proteins referred to as the telosome or shelterin complex. We here demonstrate that the isoform beta2 of the heregulin family of growth factors (HRGbeta2) is a novel interactor of the telosome/shelterin complex in human telomeres. Analysis of protein-protein interactions using a high-throughput yeast two-hybrid (Y2H) screen identified RAP1, the only telomere protein that is conserved from yeasts to mammals, as a novel interacting partner of HRGbeta2. Deletion analysis of RAP1 revealed that the linker domain, a region previously suggested to recruit negative regulators of telomere length, interacts specifically with HRGbeta2. Co-immunoprecipitation and imaging experiments demonstrated that, in addition to RAP1, HRGβ2 could associate with the RAP1-associated telomeric repeat binding factor 2 (TRF2). Deletion analysis of HRGβ2 confirmed that a putative nuclear localization signal (NLS) was necessary for nuclear HRGbeta2 to exert a negative regulation of telomere length whereas the N-terminus (extracellular) amino acids of HRGbeta2 were sufficient to interact with RAP1/TRF2 and promote telomere shortening. Taken together, our studies identify nuclear HRGbeta2 as one of the previously unknown regulators predicted to be recruited by the RAP1 linker domain to negatively regulate telomere length in human cells. Our current findings reveal that a new, but likely not the last, unexpected visitor has arrived to the "telosome/shelterin town".Fil: Menendez, Javier A.. Catalan Institute of Oncology; España. Girona Biomedical Research Institute; EspañaFil: Benboudjema, Louisa. Evanston Northwestern Healthcare Research Institute; Estados UnidosFil: Vellón, Luciano. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental (i); ArgentinaFil: Rubio, Miguel A.. Hospital de la Santa Creu i Sant Pau. Institut d’Investigació Biomèdica Sant Pau,; EspañaFil: Espinoza, Ingrid. University Of Mississippi; Estados Unidos. Lawrence Berkeley National Laboratory; Estados UnidosFil: Campisi, Judith. Lawrence Berkeley National Laboratory; Estados Unidos. Buck Institute for Research on Aging; Estados UnidosFil: Lupu, Ruth. Mayo Clinic Cancer Center; Estados Unidos. Mayo Clinic. Department of Laboratory Medicine and Pathology; Estados UnidosImpact Journals2015-07-22info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/7739Menendez, Javier A.; Benboudjema, Louisa; Vellón, Luciano; Rubio, Miguel A.; Espinoza, Ingrid; et al.; Heregulin, a new interactor of the telosome/shelterin complex in human telomeres; Impact Journals; Oncotarget; 6; 37; 22-7-2015; 39408-394211949-25531949-2553enginfo:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741835/info:eu-repo/semantics/altIdentifier/doi/10.18632/oncotarget.4962info:eu-repo/semantics/altIdentifier/url/http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path[]=4962&pubmed-linkout=1info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-01-14T11:57:15Zoai:ri.conicet.gov.ar:11336/7739instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-01-14 11:57:15.237CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
title Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
spellingShingle Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
Menendez, Javier A.
TRF2
HEREGULIN
SHELTERING COMPLEX
TELOMERE
TELOSOME
title_short Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
title_full Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
title_fullStr Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
title_full_unstemmed Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
title_sort Heregulin, a new interactor of the telosome/shelterin complex in human telomeres
dc.creator.none.fl_str_mv Menendez, Javier A.
Benboudjema, Louisa
Vellón, Luciano
Rubio, Miguel A.
Espinoza, Ingrid
Campisi, Judith
Lupu, Ruth
author Menendez, Javier A.
author_facet Menendez, Javier A.
Benboudjema, Louisa
Vellón, Luciano
Rubio, Miguel A.
Espinoza, Ingrid
Campisi, Judith
Lupu, Ruth
author_role author
author2 Benboudjema, Louisa
Vellón, Luciano
Rubio, Miguel A.
Espinoza, Ingrid
Campisi, Judith
Lupu, Ruth
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv TRF2
HEREGULIN
SHELTERING COMPLEX
TELOMERE
TELOSOME
topic TRF2
HEREGULIN
SHELTERING COMPLEX
TELOMERE
TELOSOME
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Telomere length, shape and function depend on a complex of six core telomere-associated proteins referred to as the telosome or shelterin complex. We here demonstrate that the isoform beta2 of the heregulin family of growth factors (HRGbeta2) is a novel interactor of the telosome/shelterin complex in human telomeres. Analysis of protein-protein interactions using a high-throughput yeast two-hybrid (Y2H) screen identified RAP1, the only telomere protein that is conserved from yeasts to mammals, as a novel interacting partner of HRGbeta2. Deletion analysis of RAP1 revealed that the linker domain, a region previously suggested to recruit negative regulators of telomere length, interacts specifically with HRGbeta2. Co-immunoprecipitation and imaging experiments demonstrated that, in addition to RAP1, HRGβ2 could associate with the RAP1-associated telomeric repeat binding factor 2 (TRF2). Deletion analysis of HRGβ2 confirmed that a putative nuclear localization signal (NLS) was necessary for nuclear HRGbeta2 to exert a negative regulation of telomere length whereas the N-terminus (extracellular) amino acids of HRGbeta2 were sufficient to interact with RAP1/TRF2 and promote telomere shortening. Taken together, our studies identify nuclear HRGbeta2 as one of the previously unknown regulators predicted to be recruited by the RAP1 linker domain to negatively regulate telomere length in human cells. Our current findings reveal that a new, but likely not the last, unexpected visitor has arrived to the "telosome/shelterin town".
Fil: Menendez, Javier A.. Catalan Institute of Oncology; España. Girona Biomedical Research Institute; España
Fil: Benboudjema, Louisa. Evanston Northwestern Healthcare Research Institute; Estados Unidos
Fil: Vellón, Luciano. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental (i); Argentina
Fil: Rubio, Miguel A.. Hospital de la Santa Creu i Sant Pau. Institut d’Investigació Biomèdica Sant Pau,; España
Fil: Espinoza, Ingrid. University Of Mississippi; Estados Unidos. Lawrence Berkeley National Laboratory; Estados Unidos
Fil: Campisi, Judith. Lawrence Berkeley National Laboratory; Estados Unidos. Buck Institute for Research on Aging; Estados Unidos
Fil: Lupu, Ruth. Mayo Clinic Cancer Center; Estados Unidos. Mayo Clinic. Department of Laboratory Medicine and Pathology; Estados Unidos
description Telomere length, shape and function depend on a complex of six core telomere-associated proteins referred to as the telosome or shelterin complex. We here demonstrate that the isoform beta2 of the heregulin family of growth factors (HRGbeta2) is a novel interactor of the telosome/shelterin complex in human telomeres. Analysis of protein-protein interactions using a high-throughput yeast two-hybrid (Y2H) screen identified RAP1, the only telomere protein that is conserved from yeasts to mammals, as a novel interacting partner of HRGbeta2. Deletion analysis of RAP1 revealed that the linker domain, a region previously suggested to recruit negative regulators of telomere length, interacts specifically with HRGbeta2. Co-immunoprecipitation and imaging experiments demonstrated that, in addition to RAP1, HRGβ2 could associate with the RAP1-associated telomeric repeat binding factor 2 (TRF2). Deletion analysis of HRGβ2 confirmed that a putative nuclear localization signal (NLS) was necessary for nuclear HRGbeta2 to exert a negative regulation of telomere length whereas the N-terminus (extracellular) amino acids of HRGbeta2 were sufficient to interact with RAP1/TRF2 and promote telomere shortening. Taken together, our studies identify nuclear HRGbeta2 as one of the previously unknown regulators predicted to be recruited by the RAP1 linker domain to negatively regulate telomere length in human cells. Our current findings reveal that a new, but likely not the last, unexpected visitor has arrived to the "telosome/shelterin town".
publishDate 2015
dc.date.none.fl_str_mv 2015-07-22
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/7739
Menendez, Javier A.; Benboudjema, Louisa; Vellón, Luciano; Rubio, Miguel A.; Espinoza, Ingrid; et al.; Heregulin, a new interactor of the telosome/shelterin complex in human telomeres; Impact Journals; Oncotarget; 6; 37; 22-7-2015; 39408-39421
1949-2553
1949-2553
url http://hdl.handle.net/11336/7739
identifier_str_mv Menendez, Javier A.; Benboudjema, Louisa; Vellón, Luciano; Rubio, Miguel A.; Espinoza, Ingrid; et al.; Heregulin, a new interactor of the telosome/shelterin complex in human telomeres; Impact Journals; Oncotarget; 6; 37; 22-7-2015; 39408-39421
1949-2553
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741835/
info:eu-repo/semantics/altIdentifier/doi/10.18632/oncotarget.4962
info:eu-repo/semantics/altIdentifier/url/http://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path[]=4962&pubmed-linkout=1
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Impact Journals
publisher.none.fl_str_mv Impact Journals
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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