Evidence map›Paper›PMID 26687360›Full record

ArticleCell2015

Ig Superfamily Ligand and Receptor Pairs Expressed in Synaptic Partners in Drosophila.

Liming Tan, Kelvin Xi Zhang, Matthew Y Pecot, Sonal Nagarkar-Jaiswal, Pei-Tseng Lee, Shin-Ya Takemura, Jason M McEwen, Aljoscha Nern, Shuwa Xu, Wael Tadros and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

108 citing papers in PubMed, 218 citations in OpenAlex.

  1. eLife · 2026
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  10. bioRxiv : the preprint server for biology · 2025
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  19. iScience · 2024
    Article
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48 more citing papers are in PubMed but not listed here.

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

15 authors at 6 institutions in 2 countries.

Liming TanDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Kelvin Xi ZhangDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Matthew Y PecotDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Sonal Nagarkar-JaiswalDepartment of Molecular and Human Genetics, HHMI, Baylor College of Medicine, Houston, TX 77030, USA.
Pei-Tseng LeeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Shin-Ya TakemuraJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
Jason M McEwenDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Aljoscha NernJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.
Shuwa XuDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Wael TadrosDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Zhenqing ChenDepartment of Biology, New York University, 100 Washington Square East, New York, NY 10003, USA.
Kai ZinnDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Hugo J BellenDepartment of Molecular and Human Genetics, HHMI, Baylor College of Medicine, Houston, TX 77030, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Marta MoreyDepartament de Genètica, Facultat de Biologia and Institut de Biomedicina (IBUB) de la Universitat de Barcelona, Barcelona 08028, Spain. Electronic address: mmorey@ub.edu.
S Lawrence ZipurskyDepartment of Biological Chemistry, HHMI, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA. Electronic address: lzipursky@mednet.ucla.edu.
University of California, Los Angeles · USBaylor College of Medicine · USHoward Hughes Medical Institute · USCalifornia Institute of Technology · USNew York University · USUniversitat de Barcelona · ES

Funding

Transposon induced disruption of most Drosophila genesR01GM067858 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2003 to 2020
$15.7M
MOLECULAR GENETICS OF DROSOPHILA CNS DEVELOPMENTR01NS028182 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI Engin Ozkan, KAI G ZINN · 1990 to 2026
$7.3M
Molecular Genetics of CNS DevelopmentR37NS028182 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ZINN, KAI G · 2014 to 2020
$3.3M
Synaptic target selection in DrosophilaR01NS062821 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ZINN, KAI G · 2009 to 2013
$2.1M
CIHRHoward Hughes Medical InstituteNIGMS NIH HHS R01 GM067858NIGMS NIH HHS R01GM067858NINDS NIH HHS R01 NS028182NINDS NIH HHS R01 NS062821NINDS NIH HHS R01NS28182NINDS NIH HHS R01NS62821NINDS NIH HHS R37 NS028182
6 · The paper itself

Abstract

Information processing relies on precise patterns of synapses between neurons. The cellular recognition mechanisms regulating this specificity are poorly understood. In the medulla of the Drosophila visual system, different neurons form synaptic connections in different layers. Here, we sought to identify candidate cell recognition molecules underlying this specificity. Using RNA sequencing (RNA-seq), we show that neurons with different synaptic specificities express unique combinations of mRNAs encoding hundreds of cell surface and secreted proteins. Using RNA-seq and protein tagging, we demonstrate that 21 paralogs of the Dpr family, a subclass of immunoglobulin (Ig)-domain containing proteins, are expressed in unique combinations in homologous neurons with different layer-specific synaptic connections. Dpr interacting proteins (DIPs), comprising nine paralogs of another subclass of Ig-containing proteins, are expressed in a complementary layer-specific fashion in a subset of synaptic partners. We propose that pairs of Dpr/DIP paralogs contribute to layer-specific patterns of synaptic connectivity.

Indexed as

SynapsesAnimalsDrosophilaDrosophila ProteinsFlow CytometryImmunoglobulinsNeuronsReceptors, ImmunologicSequence Analysis, RNAVision, OcularDPR1 protein, DrosophilaDrosophila ProteinsImmunoglobulinsReceptors, ImmunologicDIPDprDrosophilasynaptic specificityvisual system

Identifiers

PMID26687360
PMCPMC4804707
OpenAlexW2213906369

What OpenQuestion holds

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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.