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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/266383

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network_name_str CONICET Digital (CONICET)
spelling 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)
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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