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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/7739
Ver los metadatos del registro completo
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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 |
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article |
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publishedVersion |
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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 |
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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 |
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openAccess |
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