Evidence map›Paper›PMID 34731636›Full record

ArticleCell reports2021

Molecular and structural basis of olfactory sensory neuron axon coalescence by Kirrel receptors.

Jing Wang, Neelima Vaddadi, Joseph S Pak, Yeonwoo Park, Sabrina Quilez, Christina A Roman, Emilie Dumontier, Joseph W Thornton, Jean-François Cloutier, Engin Özkan

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  12. Structure and evolution of neuronal wiring receptors and ligands.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
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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

10 authors at 3 institutions in 2 countries.

Jing WangDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA; Grossman Institute for Neuroscience, Quantitative Biology and Human Behavior, The University of Chicago, Chicago, IL 60637, USA.
Neelima VaddadiThe Neuro-Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 2B4, Canada.
Joseph S PakDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA; Grossman Institute for Neuroscience, Quantitative Biology and Human Behavior, The University of Chicago, Chicago, IL 60637, USA.
Yeonwoo ParkCommittee on Genetics, Genomics and Systems Biology, The University of Chicago, Chicago, IL 60637, USA.
Sabrina QuilezThe Neuro-Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 2B4, Canada.
Christina A RomanDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA.
Emilie DumontierThe Neuro-Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada.
Joseph W ThorntonCommittee on Genetics, Genomics and Systems Biology, The University of Chicago, Chicago, IL 60637, USA; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA; Department of Ecology and Evolution, The University of Chicago, Chicago, IL 60637, USA.
Jean-François CloutierThe Neuro-Montreal Neurological Institute and Hospital, McGill University, Montréal, QC H3A 2B4, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC H3A 2B4, Canada; Department of Anatomy and Cell Biology, McGill University, Montréal, QC H3A 0C7, Canada. Electronic address: jf.cloutier@mcgill.ca.
Engin ÖzkanDepartment of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA; Grossman Institute for Neuroscience, Quantitative Biology and Human Behavior, The University of Chicago, Chicago, IL 60637, USA. Electronic address: eozkan@uchicago.edu.
University of Chicago · USMontreal Neurological Institute and Hospital · CAMcGill University · CA

Funding

User Training and OutreachP30GM124165 · NIGMS · CORNELL UNIVERSITY · PI Nozomi Ando, J Christopher Fromme · 2018 to 2026
$34.2M
X-ray Absorption Spectroscopy (XAS) pp.711-759P41GM103393 · NIGMS · STANFORD UNIVERSITY · PI HODGSON, KEITH O · 2012 to 2019
$30.6M
Time resolved SAXS studies on the RP2/Arl3 complex pp.484-485P41GM103622 · NIGMS · ILLINOIS INSTITUTE OF TECHNOLOGY · PI IRVING, THOMAS C · 2012 to 2020
$11.9M
Comprehensive analysis of fitness effects and epistasis along a billion-year evolutionary trajectoryR01GM139007 · NIGMS · UNIVERSITY OF CHICAGO · PI BOLON, DANIEL N, THORNTON, JOSEPH W · 2021 to 2024
$2.2M
Molecular Recognition Principles, Engineering and Function of Neural Wiring ReceptorsR01NS097161 · NINDS · UNIVERSITY OF CHICAGO · PI OZKAN, ENGIN · 2016 to 2020
$1.8M
Deep characterization of the sequence space and evolutionary trajectories of reconstructed ancestral proteins - Resubmission 01R01GM121931 · NIGMS · UNIVERSITY OF CHICAGO · PI THORNTON, JOSEPH W · 2017 to 2020
$1.3M
Evolution of molecular complexes: genetic, structural, and functional mechanisms for the evolution of oligomers and allosteryR01GM131128 · NIGMS · UNIVERSITY OF CHICAGO · PI THORNTON, JOSEPH W · 2019 to 2021
$904k
Advanced Pixel Array Detector for Time-Resolved SAXS and Fiber DiffractionS10OD018090 · OD · ILLINOIS INSTITUTE OF TECHNOLOGY · PI IRVING, THOMAS C · 2014 to 2014
$529k
CIHR MOP-136872NIGMS NIH HHS P30 GM124165NIGMS NIH HHS P41 GM103393NIGMS NIH HHS P41 GM103622NIGMS NIH HHS R01 GM121931NIGMS NIH HHS R01 GM131128NIGMS NIH HHS R01 GM139007NIH HHS S10 OD018090NINDS NIH HHS R01 NS097161
6 · The paper itself

Abstract

Projections from sensory neurons of olfactory systems coalesce into glomeruli in the brain. The Kirrel receptors are believed to homodimerize via their ectodomains and help separate sensory neuron axons into Kirrel2- or Kirrel3-expressing glomeruli. Here, we present the crystal structures of homodimeric Kirrel receptors and show that the closely related Kirrel2 and Kirrel3 have evolved specific sets of polar and hydrophobic interactions, respectively, disallowing heterodimerization while preserving homodimerization, likely resulting in proper segregation and coalescence of Kirrel-expressing axons into glomeruli. We show that the dimerization interface at the N-terminal immunoglobulin (IG) domains is necessary and sufficient to create homodimers and fail to find evidence for a secondary interaction site in Kirrel ectodomains. Furthermore, we show that abolishing dimerization of Kirrel3 in vivo leads to improper formation of glomeruli in the mouse accessory olfactory bulb as observed in Kirrel3

Indexed as

SmellAnimalsAxonsEvolution, MolecularHEK293 CellsHumansImmunoglobulinsMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutModels, MolecularMutationOdorantsOlfactory BulbOlfactory Receptor NeuronsImmunoglobulinsKirrel3 protein, mouseMembrane ProteinsNeph3 protein, mouseReceptors, Odorantaccessory olfactory systemaxonal coalescencecell adhesion moleculeglomeruliKirrel2Kirrel3protein structurevomeronasal

Identifiers

PMID34731636
PMCPMC8628261
OpenAlexW3208816664

What OpenQuestion holds

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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.