Evidence map›Paper›PMID 36271407›Full record

ArticleNeural development2022

Dpr10 and Nocte are required for Drosophila motor axon pathfinding.

Meike Lobb-Rabe, Katherine DeLong, Rio J Salazar, Ruiling Zhang, Yupu Wang, Robert A Carrillo

Open access · goldAbstract read
In one paragraph

Article in Neural development, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Zoological research · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. bioRxiv : the preprint server for biology · 2023
    Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Meike Lobb-Rabe *Department of Molecular Genetics & Cellular Biology, University of Chicago, Chicago, IL, 60637, USA.ORCID 0000-0001-6486-7752
Katherine DeLong *Department of Molecular Genetics & Cellular Biology, University of Chicago, Chicago, IL, 60637, USA.
Rio J SalazarDepartment of Molecular Genetics & Cellular Biology, University of Chicago, Chicago, IL, 60637, USA.ORCID 0000-0001-9606-7792
Ruiling ZhangDepartment of Molecular Genetics & Cellular Biology, University of Chicago, Chicago, IL, 60637, USA.ORCID 0000-0001-8523-1796
Yupu WangDepartment of Molecular Genetics & Cellular Biology, University of Chicago, Chicago, IL, 60637, USA.ORCID 0000-0002-3553-0680
Robert A CarrilloDepartment of Molecular Genetics & Cellular Biology, University of Chicago, Chicago, IL, 60637, USA. robertcarrillo@uchicago.edu.ORCID 0000-0002-2067-9861
University of Chicago · USUniversity of Illinois Chicago · US

Funding

Molecular And Cellular Biology Training ProgramT32GM007183 · NIGMS · UNIVERSITY OF CHICAGO · PI GLICK, BENJAMIN S, RICE, PHOEBE A · 1985 to 2021
$23.9M
UNIVERSITY OF CHICAGO PREPR25GM066522 · NIGMS · UNIVERSITY OF CHICAGO · PI CARRILLO, ROBERT ARNULFO, RANDALL, GLENN C · 2004 to 2024
$6.7M
University of Chicago Initiative for Maximizing Student Development (IMSD) - Renewal 01R25GM109439 · NIGMS · UNIVERSITY OF CHICAGO · PI SCHWARTZ, NANCY B · 2014 to 2023
$5.7M
IgSF protein interactions drive specificity in circuit wiring and synaptic elaborationR01NS123439 · NINDS · UNIVERSITY OF CHICAGO · PI CARRILLO, ROBERT ARNULFO · 2021 to 2025
$2.1M
DIP-α is required for synaptic elaboration and functionF31NS120458 · NINDS · UNIVERSITY OF CHICAGO · PI LOBB-RABE, MEIKE · 2020 to 2022
$127k
NIGMS NIH HHS R25 GM066522NIGMS NIH HHS R25 GM109439NIGMS NIH HHS T32 GM007183NINDS NIH HHS F31 NS120458NINDS NIH HHS R01 NS123439
6 · The paper itself

Abstract

The paths axons travel to reach their targets and the subsequent synaptic connections they form are highly stereotyped. How cell surface proteins (CSPs) mediate these processes is not completely understood. The Drosophila neuromuscular junction (NMJ) is an ideal system to study how pathfinding and target specificity are accomplished, as the axon trajectories and innervation patterns are known and easily visualized. Dpr10 is a CSP required for synaptic partner choice in the neuromuscular and visual circuits and for axon pathfinding in olfactory neuron organization. In this study, we show that Dpr10 is also required for motor axon pathfinding. To uncover how Dpr10 mediates this process, we used immunoprecipitation followed by mass spectrometry to identify Dpr10 associated proteins. One of these, Nocte, is an unstructured, intracellular protein implicated in circadian rhythm entrainment. We mapped nocte expression in larvae and found it widely expressed in neurons, muscles, and glia. Cell-specific knockdown suggests nocte is required presynaptically to mediate motor axon pathfinding. Additionally, we found that nocte and dpr10 genetically interact to control NMJ assembly, suggesting that they function in the same molecular pathway. Overall, these data reveal novel roles for Dpr10 and its newly identified interactor, Nocte, in motor axon pathfinding and provide insight into how CSPs regulate circuit assembly.

Indexed as

DrosophilaDrosophila ProteinsAnimalsAxon GuidanceAxonsMembrane ProteinsMotor NeuronsDrosophila ProteinsMembrane Proteins

Identifiers

PMID36271407
PMCPMC9585758
OpenAlexW4306964179

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.