Evidence map›Paper›PMID 38585986›Full record

ArticlebioRxiv : the preprint server for biology2024

Trafficking of Connexin36 (Cx36) in the early secretory pathway.

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

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Stephan TetenborgCollege of Optometry, University of Houston, Houston, TX, USA.
Fatemeh AriakiaCollege of Optometry, University of Houston, Houston, TX, USA.
Elizabeth Martinez-SolerCollege of Optometry, University of Houston, Houston, TX, USA.
Eyad ShihabeddinCollege of Optometry, University of Houston, Houston, TX, USA.
Ignacio Cebrian LazartInstituto de Histología y Embriología de Mendoza (IHEM)-CONICET, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Mendoza 5500, 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.ORCID 0000-0002-0270-3442
University of Houston · USThe University of Texas MD Anderson Cancer Center · USUniversidad Nacional de Cuyo · ARUniversity of Oregon · US

Funding

Research Programming ModuleP30EY007551 · NEI · UNIVERSITY OF HOUSTON · PI VALLABH E DAS · 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
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
NCATS NIH HHS TL1 TR003169NEI NIH HHS F31 EY034793NEI NIH HHS P30 EY007551NEI NIH HHS R01 EY012857NINDS NIH HHS R01 NS105758
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 activities or 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.

Identifiers

PMID38585986
PMCPMC10996632
OpenAlexW4393277702

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.