Evidence map›Paper›PMID 38915497›Full record

ArticlebioRxiv : the preprint server for biology2024

CCSer2 gates dynein activity at the cell periphery.

Juliana L Zang, Daytan Gibson, Ann-Marie Zheng, Wanjing Shi, John P Gillies, Chris Stein, Catherine M Drerup, Morgan E DeSantis

Abstract 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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Juliana L ZangDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Daytan GibsonDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Ann-Marie ZhengDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Wanjing ShiDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
John P GilliesDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.
Chris SteinDepartment of Integrative Biology, University of Wisconsin-Madison, Madison, WI 53706.
Catherine M DrerupDepartment of Integrative Biology, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0002-0219-3075
Morgan E DeSantisDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0002-4096-8548

Funding

Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
Mechanisms of dynein regulationR35GM146739 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Morgan DeSantis · 2022 to 2026
$1.7M
Mechanisms of Lis1 and NudE/L Regulation of the Molecular Motor DyneinR00GM127757 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DESANTIS, MORGAN · 2020 to 2022
$747k
NIGMS NIH HHS R00 GM127757NIGMS NIH HHS R35 GM146739NIGMS NIH HHS T32 GM145304
6 · The paper itself

Abstract

Cytoplasmic dynein-1 (dynein) is a microtubule-associated, minus end-directed motor that traffics hundreds of different cargos. Dynein must discriminate between cargos and traffic them at the appropriate time from the correct cellular region. How dynein's trafficking activity is regulated in time or cellular space remains poorly understood. Here, we identify CCSer2 as the first known protein to gate dynein activity in the spatial dimension. CCSer2 promotes the migration of developing zebrafish primordium cells and of cultured human cells by facilitating the trafficking of cargos that are acted on by cortically localized dynein. CCSer2 inhibits the interaction between dynein and its regulator Ndel1 exclusively at the cell periphery, resulting in localized dynein activation. Our findings suggest that the spatial specificity of dynein is achieved by the localization of proteins that disinhibit Ndel1. We propose that CCSer2 defines a broader class of proteins that activate dynein in distinct microenvironments via Ndel1 inhibition.

Indexed as

CCSer2DyneinmigrationNdel1

Identifiers

PMID38915497
PMCPMC11195223

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.