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Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A

Variants in the high confident autism spectrum disorder (ASD) gene ANK2 target both ubiquitously expressed 220 kDa ankyrin-B and neurospecific 440 kDa ankyrin-B (AnkB440) isoforms. Previous work showed that knock-in mice expressing an ASD-linked Ank2 variant yielding a truncated AnkB440 product exhi...

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Autores principales: Creighton, Blake A, Afriyie, Simone, Ajit, Deepa, Casingal, Cristine R, Voos, Kayleigh M, Reger, Joan, Burch, April M, Dyne, Eric, Bay, Julia, Huang, Jeffrey K, Anton, ES, Fu, Meng-Meng, Lorenzo, Damaris N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610419/
https://www.ncbi.nlm.nih.gov/pubmed/34812142
http://dx.doi.org/10.7554/eLife.69815
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author Creighton, Blake A
Afriyie, Simone
Ajit, Deepa
Casingal, Cristine R
Voos, Kayleigh M
Reger, Joan
Burch, April M
Dyne, Eric
Bay, Julia
Huang, Jeffrey K
Anton, ES
Fu, Meng-Meng
Lorenzo, Damaris N
author_facet Creighton, Blake A
Afriyie, Simone
Ajit, Deepa
Casingal, Cristine R
Voos, Kayleigh M
Reger, Joan
Burch, April M
Dyne, Eric
Bay, Julia
Huang, Jeffrey K
Anton, ES
Fu, Meng-Meng
Lorenzo, Damaris N
author_sort Creighton, Blake A
collection PubMed
description Variants in the high confident autism spectrum disorder (ASD) gene ANK2 target both ubiquitously expressed 220 kDa ankyrin-B and neurospecific 440 kDa ankyrin-B (AnkB440) isoforms. Previous work showed that knock-in mice expressing an ASD-linked Ank2 variant yielding a truncated AnkB440 product exhibit ectopic brain connectivity and behavioral abnormalities. Expression of this variant or loss of AnkB440 caused axonal hyperbranching in vitro, which implicated AnkB440 microtubule bundling activity in suppressing collateral branch formation. Leveraging multiple mouse models, cellular assays, and live microscopy, we show that AnkB440 also modulates axon collateral branching stochastically by reducing the number of F-actin-rich branch initiation points. Additionally, we show that AnkB440 enables growth cone (GC) collapse in response to chemorepellent factor semaphorin 3 A (Sema 3 A) by stabilizing its receptor complex L1 cell adhesion molecule/neuropilin-1. ASD-linked ANK2 variants failed to rescue Sema 3A-induced GC collapse. We propose that impaired response to repellent cues due to AnkB440 deficits leads to axonal targeting and branch pruning defects and may contribute to the pathogenicity of ANK2 variants.
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spelling pubmed-86104192021-11-24 Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A Creighton, Blake A Afriyie, Simone Ajit, Deepa Casingal, Cristine R Voos, Kayleigh M Reger, Joan Burch, April M Dyne, Eric Bay, Julia Huang, Jeffrey K Anton, ES Fu, Meng-Meng Lorenzo, Damaris N eLife Cell Biology Variants in the high confident autism spectrum disorder (ASD) gene ANK2 target both ubiquitously expressed 220 kDa ankyrin-B and neurospecific 440 kDa ankyrin-B (AnkB440) isoforms. Previous work showed that knock-in mice expressing an ASD-linked Ank2 variant yielding a truncated AnkB440 product exhibit ectopic brain connectivity and behavioral abnormalities. Expression of this variant or loss of AnkB440 caused axonal hyperbranching in vitro, which implicated AnkB440 microtubule bundling activity in suppressing collateral branch formation. Leveraging multiple mouse models, cellular assays, and live microscopy, we show that AnkB440 also modulates axon collateral branching stochastically by reducing the number of F-actin-rich branch initiation points. Additionally, we show that AnkB440 enables growth cone (GC) collapse in response to chemorepellent factor semaphorin 3 A (Sema 3 A) by stabilizing its receptor complex L1 cell adhesion molecule/neuropilin-1. ASD-linked ANK2 variants failed to rescue Sema 3A-induced GC collapse. We propose that impaired response to repellent cues due to AnkB440 deficits leads to axonal targeting and branch pruning defects and may contribute to the pathogenicity of ANK2 variants. eLife Sciences Publications, Ltd 2021-11-23 /pmc/articles/PMC8610419/ /pubmed/34812142 http://dx.doi.org/10.7554/eLife.69815 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Cell Biology
Creighton, Blake A
Afriyie, Simone
Ajit, Deepa
Casingal, Cristine R
Voos, Kayleigh M
Reger, Joan
Burch, April M
Dyne, Eric
Bay, Julia
Huang, Jeffrey K
Anton, ES
Fu, Meng-Meng
Lorenzo, Damaris N
Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
title Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
title_full Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
title_fullStr Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
title_full_unstemmed Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
title_short Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
title_sort giant ankyrin-b mediates transduction of axon guidance and collateral branch pruning factor sema 3a
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610419/
https://www.ncbi.nlm.nih.gov/pubmed/34812142
http://dx.doi.org/10.7554/eLife.69815
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