Evidence map›Paper›PMID 39395036›Full record

ArticleCellular and molecular life sciences : CMLS2024

Regulation of Cx36 trafficking through the early secretory pathway by COPII cargo receptors and Grasp55.

Stephan Tetenborg, Fatemeh Ariakia, Elizabeth Martinez-Soler, Eyad Shihabeddin, Ignacio Cebrian Lazart, Adam C Miller, John O'Brien

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Stephan TetenborgCollege of Optometry, University of Houston, Houston, TX, USA. stetenbo@Central.UH.EDU.ORCID http://orcid.org/0000-0002-9025-0446
Fatemeh Ariakia *College of Optometry, University of Houston, Houston, TX, USA.
Elizabeth Martinez-Soler *College of Optometry, University of Houston, Houston, TX, USA.
Eyad ShihabeddinCollege of Optometry, University of Houston, Houston, TX, USA.
Ignacio Cebrian LazartFacultad de Ciencias Médicas, Instituto de Histología y Embriología de Mendoza (IHEM)-CONICET, Universidad Nacional de Cuyo, 5500, Mendoza, Argentina.
Adam C MillerInstitute of Neuroscience, Department of Biology, University of Oregon, Eugene, OR, USA.
John O'BrienCollege of Optometry, University of Houston, Houston, TX, USA. jobrien3@Central.UH.EDU.

Funding

Research Programming ModuleP30EY007551 · NEI · UNIVERSITY OF HOUSTON · PI Nimesh Bhikhu Patel · 1988 to 2026
$16.4M
REGULATION OF RETINAL GAP JUNCTIONSR01EY012857 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JOHN O'BRIEN · 2000 to 2026
$8.3M
Molecular Mechanisms of Electrical Synapse Formation in VivoR01NS105758 · NINDS · UNIVERSITY OF OREGON · PI Adam C Miller · 2019 to 2026
$3.7M
NRSA Training CoreTL1TR003169 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHANDRA, JOYA, FROST, JEFFREY A. · 2019 to 2023
$3.7M
UTHouston Core Center for Vision ResearchP30EY028102 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DRAGOI, VALENTIN · 2017 to 2021
$3.1M
Genetic Factors Mediating Thyroid Hormone-Induced Opsin Switching in Zebrafish Cone PhotoreceptorsF31EY031962 · NEI · UNIVERSITY OF IDAHO · PI FARRE, ASHLEY ALICE · 2020 to 2022
$98k
Rod photoreceptor regeneration in a zebrafish model of Retinitis Pigmentosa.F31EY034793 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI SHIHABEDDIN, EYAD · 2023 to 2025
$82k
Deutsche Forschungsgemeinschaft TE 1459/1-1NCATS NIH HHS TL1 TR003169NEI NIH HHS F31 EY031962NEI NIH HHS F31 EY034793NEI NIH HHS P30 EY007551NEI NIH HHS P30 EY028102NEI NIH HHS R01 EY012857NEI NIH HHS R01EY012857NIH HHS F31EY034793NINDS NIH HHS R01 NS105758NINDS NIH HHS R01NS105758
6 · The paper itself

Abstract

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 significance 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 effects 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.

Indexed as

ConnexinsCOP-Coated VesiclesGolgi Matrix ProteinsMembrane ProteinsProtein TransportEndoplasmic ReticulumGap JunctionsGolgi ApparatusHEK293 CellsHumansProtein BindingRNA, Small InterferingSecretory PathwayVesicular Transport ProteinsConnexinsGolgi Matrix ProteinsGORASP1 protein, humanMembrane ProteinsRNA, Small InterferingSEC24A protein, humanSEC24C protein, humanSEC24D protein, humanVesicular Transport ProteinsCx36ER exportPDZ domain

Identifiers

PMID39395036
PMCPMC11470877

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.