Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55
- Autores
- Tetenborg, Stephan; Ariakia, Fatemeh; Martinez Soler, Elizabeth; Shihabeddin, Eyad; Cebrián, José Ignacio; Miller, Adam C.; O'Brien, John
- Año de publicación
- 2024
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Gap junctions formed by the major neuronal connexin Cx36 function as electrical synapses in the nervous system and provide unique functions such as synchronizing neuron activities or supporting network oscillations. Although the physiological signifcance of electrical synapses for neuronal networks is well established, little is known about the pathways that regulate the transport of its main component: Cx36. Here we have used HEK293T cells as an expression system in combination with siRNA and BioID screens to study the transition of Cx36 from the ER to the cis Golgi. Our data indicate that the C-terminal tip of Cx36 is a key factor in this process, mediating binding interactions with two distinct components in the early secretory pathway: the COPII complex and the Golgi stacking protein Grasp55. The C-terminal amino acid valine serves as an ER export signal to recruit COPII cargo receptors Sec24A/B/C at ER exit sites, whereas the PDZ binding motif “SAYV” mediates an interaction with Grasp55. These two interactions have opposing efects in their respective compartments. While Sec24 subunits carry Cx36 out of the ER, Grasp55 stabilizes Cx36 in the Golgi as shown in over expression experiments. These early regulatory steps of Cx36 are expected to be essential for the formation, function, regulation and plasticity of electrical synapses in the developing and mature nervous system.
Fil: Tetenborg, Stephan. University Of Houston; Estados Unidos
Fil: Ariakia, Fatemeh. University Of Houston; Estados Unidos
Fil: Martinez Soler, Elizabeth. University Of Houston; Estados Unidos
Fil: Shihabeddin, Eyad. University Of Houston; Estados Unidos. University of Texas Health Science Center at Houston. University of Texas Md Anderson Cancer Center; Estados Unidos
Fil: Cebrián, José Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina
Fil: Miller, Adam C.. University of Oregon; Estados Unidos
Fil: O'Brien, John. University Of Houston; Estados Unidos - Materia
-
CX36
ER EXPORT
PDZ DOMAIN - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/266383
Ver los metadatos del registro completo
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Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55Tetenborg, StephanAriakia, FatemehMartinez Soler, ElizabethShihabeddin, EyadCebrián, José IgnacioMiller, Adam C.O'Brien, JohnCX36ER EXPORTPDZ DOMAINhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1https://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Gap junctions formed by the major neuronal connexin Cx36 function as electrical synapses in the nervous system and provide unique functions such as synchronizing neuron activities or supporting network oscillations. Although the physiological signifcance of electrical synapses for neuronal networks is well established, little is known about the pathways that regulate the transport of its main component: Cx36. Here we have used HEK293T cells as an expression system in combination with siRNA and BioID screens to study the transition of Cx36 from the ER to the cis Golgi. Our data indicate that the C-terminal tip of Cx36 is a key factor in this process, mediating binding interactions with two distinct components in the early secretory pathway: the COPII complex and the Golgi stacking protein Grasp55. The C-terminal amino acid valine serves as an ER export signal to recruit COPII cargo receptors Sec24A/B/C at ER exit sites, whereas the PDZ binding motif “SAYV” mediates an interaction with Grasp55. These two interactions have opposing efects in their respective compartments. While Sec24 subunits carry Cx36 out of the ER, Grasp55 stabilizes Cx36 in the Golgi as shown in over expression experiments. These early regulatory steps of Cx36 are expected to be essential for the formation, function, regulation and plasticity of electrical synapses in the developing and mature nervous system.Fil: Tetenborg, Stephan. University Of Houston; Estados UnidosFil: Ariakia, Fatemeh. University Of Houston; Estados UnidosFil: Martinez Soler, Elizabeth. University Of Houston; Estados UnidosFil: Shihabeddin, Eyad. University Of Houston; Estados Unidos. University of Texas Health Science Center at Houston. University of Texas Md Anderson Cancer Center; Estados UnidosFil: Cebrián, José Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; ArgentinaFil: Miller, Adam C.. University of Oregon; Estados UnidosFil: O'Brien, John. University Of Houston; Estados UnidosSpringer2024-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/266383Tetenborg, Stephan; Ariakia, Fatemeh; Martinez Soler, Elizabeth; Shihabeddin, Eyad; Cebrián, José Ignacio; et al.; Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55; Springer; Cellular and Molecular Life Sciences; 81; 1; 10-2024; 1-171420-682XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/10.1007/s00018-024-05440-8info:eu-repo/semantics/altIdentifier/doi/10.1007/s00018-024-05440-8info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:42:38Zoai:ri.conicet.gov.ar:11336/266383instacron: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:34982025-09-29 09:42:38.523CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
title |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
spellingShingle |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 Tetenborg, Stephan CX36 ER EXPORT PDZ DOMAIN |
title_short |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
title_full |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
title_fullStr |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
title_full_unstemmed |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
title_sort |
Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55 |
dc.creator.none.fl_str_mv |
Tetenborg, Stephan Ariakia, Fatemeh Martinez Soler, Elizabeth Shihabeddin, Eyad Cebrián, José Ignacio Miller, Adam C. O'Brien, John |
author |
Tetenborg, Stephan |
author_facet |
Tetenborg, Stephan Ariakia, Fatemeh Martinez Soler, Elizabeth Shihabeddin, Eyad Cebrián, José Ignacio Miller, Adam C. O'Brien, John |
author_role |
author |
author2 |
Ariakia, Fatemeh Martinez Soler, Elizabeth Shihabeddin, Eyad Cebrián, José Ignacio Miller, Adam C. O'Brien, John |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
CX36 ER EXPORT PDZ DOMAIN |
topic |
CX36 ER EXPORT PDZ DOMAIN |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/3.1 https://purl.org/becyt/ford/3 |
dc.description.none.fl_txt_mv |
Gap junctions formed by the major neuronal connexin Cx36 function as electrical synapses in the nervous system and provide unique functions such as synchronizing neuron activities or supporting network oscillations. Although the physiological signifcance of electrical synapses for neuronal networks is well established, little is known about the pathways that regulate the transport of its main component: Cx36. Here we have used HEK293T cells as an expression system in combination with siRNA and BioID screens to study the transition of Cx36 from the ER to the cis Golgi. Our data indicate that the C-terminal tip of Cx36 is a key factor in this process, mediating binding interactions with two distinct components in the early secretory pathway: the COPII complex and the Golgi stacking protein Grasp55. The C-terminal amino acid valine serves as an ER export signal to recruit COPII cargo receptors Sec24A/B/C at ER exit sites, whereas the PDZ binding motif “SAYV” mediates an interaction with Grasp55. These two interactions have opposing efects in their respective compartments. While Sec24 subunits carry Cx36 out of the ER, Grasp55 stabilizes Cx36 in the Golgi as shown in over expression experiments. These early regulatory steps of Cx36 are expected to be essential for the formation, function, regulation and plasticity of electrical synapses in the developing and mature nervous system. Fil: Tetenborg, Stephan. University Of Houston; Estados Unidos Fil: Ariakia, Fatemeh. University Of Houston; Estados Unidos Fil: Martinez Soler, Elizabeth. University Of Houston; Estados Unidos Fil: Shihabeddin, Eyad. University Of Houston; Estados Unidos. University of Texas Health Science Center at Houston. University of Texas Md Anderson Cancer Center; Estados Unidos Fil: Cebrián, José Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos. Universidad Nacional de Cuyo. Facultad de Ciencias Médicas. Instituto de Histología y Embriología de Mendoza Dr. Mario H. Burgos; Argentina Fil: Miller, Adam C.. University of Oregon; Estados Unidos Fil: O'Brien, John. University Of Houston; Estados Unidos |
description |
Gap junctions formed by the major neuronal connexin Cx36 function as electrical synapses in the nervous system and provide unique functions such as synchronizing neuron activities or supporting network oscillations. Although the physiological signifcance of electrical synapses for neuronal networks is well established, little is known about the pathways that regulate the transport of its main component: Cx36. Here we have used HEK293T cells as an expression system in combination with siRNA and BioID screens to study the transition of Cx36 from the ER to the cis Golgi. Our data indicate that the C-terminal tip of Cx36 is a key factor in this process, mediating binding interactions with two distinct components in the early secretory pathway: the COPII complex and the Golgi stacking protein Grasp55. The C-terminal amino acid valine serves as an ER export signal to recruit COPII cargo receptors Sec24A/B/C at ER exit sites, whereas the PDZ binding motif “SAYV” mediates an interaction with Grasp55. These two interactions have opposing efects in their respective compartments. While Sec24 subunits carry Cx36 out of the ER, Grasp55 stabilizes Cx36 in the Golgi as shown in over expression experiments. These early regulatory steps of Cx36 are expected to be essential for the formation, function, regulation and plasticity of electrical synapses in the developing and mature nervous system. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-10 |
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/11336/266383 Tetenborg, Stephan; Ariakia, Fatemeh; Martinez Soler, Elizabeth; Shihabeddin, Eyad; Cebrián, José Ignacio; et al.; Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55; Springer; Cellular and Molecular Life Sciences; 81; 1; 10-2024; 1-17 1420-682X CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/266383 |
identifier_str_mv |
Tetenborg, Stephan; Ariakia, Fatemeh; Martinez Soler, Elizabeth; Shihabeddin, Eyad; Cebrián, José Ignacio; et al.; Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55; Springer; Cellular and Molecular Life Sciences; 81; 1; 10-2024; 1-17 1420-682X CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/10.1007/s00018-024-05440-8 info:eu-repo/semantics/altIdentifier/doi/10.1007/s00018-024-05440-8 |
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 |
Springer |
publisher.none.fl_str_mv |
Springer |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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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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1844613342949277696 |
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13.070432 |