Cargando…

Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function

Tunicates are marine, non-vertebrate chordates that comprise the sister group to the vertebrates. Most tunicates have a biphasic lifecycle that alternates between a swimming larva and a sessile adult. Recent advances have shed light on the neural basis for the tunicate larva’s ability to sense a pro...

Descripción completa

Detalles Bibliográficos
Autores principales: Johnson, Christopher J., Kulkarni, Akhil, Buxton, William J., Hui, Tsz Y., Kayastha, Anusha, Khoja, Alwin A., Leandre, Joviane, Mehta, Vanshika V., Ostrowski, Logan, Pareizs, Erica G., Scotto, Rebecca L., Vargas, Vanesa, Vellingiri, Raveena M., Verzino, Giulia, Vohra, Rhea, Wakade, Saurabh C., Winkeljohn, Veronica M., Winkeljohn, Victoria M., Rotterman, Travis M., Stolfi, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197531/
https://www.ncbi.nlm.nih.gov/pubmed/37214826
http://dx.doi.org/10.1101/2023.05.08.539861
_version_ 1785044570930675712
author Johnson, Christopher J.
Kulkarni, Akhil
Buxton, William J.
Hui, Tsz Y.
Kayastha, Anusha
Khoja, Alwin A.
Leandre, Joviane
Mehta, Vanshika V.
Ostrowski, Logan
Pareizs, Erica G.
Scotto, Rebecca L.
Vargas, Vanesa
Vellingiri, Raveena M.
Verzino, Giulia
Vohra, Rhea
Wakade, Saurabh C.
Winkeljohn, Veronica M.
Winkeljohn, Victoria M.
Rotterman, Travis M.
Stolfi, Alberto
author_facet Johnson, Christopher J.
Kulkarni, Akhil
Buxton, William J.
Hui, Tsz Y.
Kayastha, Anusha
Khoja, Alwin A.
Leandre, Joviane
Mehta, Vanshika V.
Ostrowski, Logan
Pareizs, Erica G.
Scotto, Rebecca L.
Vargas, Vanesa
Vellingiri, Raveena M.
Verzino, Giulia
Vohra, Rhea
Wakade, Saurabh C.
Winkeljohn, Veronica M.
Winkeljohn, Victoria M.
Rotterman, Travis M.
Stolfi, Alberto
author_sort Johnson, Christopher J.
collection PubMed
description Tunicates are marine, non-vertebrate chordates that comprise the sister group to the vertebrates. Most tunicates have a biphasic lifecycle that alternates between a swimming larva and a sessile adult. Recent advances have shed light on the neural basis for the tunicate larva’s ability to sense a proper substrate for settlement and initiate metamorphosis. Work in the highly tractable laboratory model tunicate Ciona robusta suggests that sensory neurons embedded in the anterior papillae of transduce mechanosensory stimuli to trigger larval tail retraction and initiate the process of metamorphosis. Here, we take advantage of the low-cost and simplicity of Ciona by using tissue-specific CRISPR/Cas9-mediated mutagenesis to screen for genes potentially involved in mechanosensation and metamorphosis, in the context of an undergraduate “capstone” research course. This small screen revealed at least one gene, Vamp1/2/3, that appears crucial for the ability of the papillae to trigger metamorphosis. We also provide step-by-step protocols and tutorials associated with this course, in the hope that it might be replicated in similar CRISPR-based laboratory courses wherever Ciona are available.
format Online
Article
Text
id pubmed-10197531
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-101975312023-05-20 Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function Johnson, Christopher J. Kulkarni, Akhil Buxton, William J. Hui, Tsz Y. Kayastha, Anusha Khoja, Alwin A. Leandre, Joviane Mehta, Vanshika V. Ostrowski, Logan Pareizs, Erica G. Scotto, Rebecca L. Vargas, Vanesa Vellingiri, Raveena M. Verzino, Giulia Vohra, Rhea Wakade, Saurabh C. Winkeljohn, Veronica M. Winkeljohn, Victoria M. Rotterman, Travis M. Stolfi, Alberto bioRxiv Article Tunicates are marine, non-vertebrate chordates that comprise the sister group to the vertebrates. Most tunicates have a biphasic lifecycle that alternates between a swimming larva and a sessile adult. Recent advances have shed light on the neural basis for the tunicate larva’s ability to sense a proper substrate for settlement and initiate metamorphosis. Work in the highly tractable laboratory model tunicate Ciona robusta suggests that sensory neurons embedded in the anterior papillae of transduce mechanosensory stimuli to trigger larval tail retraction and initiate the process of metamorphosis. Here, we take advantage of the low-cost and simplicity of Ciona by using tissue-specific CRISPR/Cas9-mediated mutagenesis to screen for genes potentially involved in mechanosensation and metamorphosis, in the context of an undergraduate “capstone” research course. This small screen revealed at least one gene, Vamp1/2/3, that appears crucial for the ability of the papillae to trigger metamorphosis. We also provide step-by-step protocols and tutorials associated with this course, in the hope that it might be replicated in similar CRISPR-based laboratory courses wherever Ciona are available. Cold Spring Harbor Laboratory 2023-05-08 /pmc/articles/PMC10197531/ /pubmed/37214826 http://dx.doi.org/10.1101/2023.05.08.539861 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Johnson, Christopher J.
Kulkarni, Akhil
Buxton, William J.
Hui, Tsz Y.
Kayastha, Anusha
Khoja, Alwin A.
Leandre, Joviane
Mehta, Vanshika V.
Ostrowski, Logan
Pareizs, Erica G.
Scotto, Rebecca L.
Vargas, Vanesa
Vellingiri, Raveena M.
Verzino, Giulia
Vohra, Rhea
Wakade, Saurabh C.
Winkeljohn, Veronica M.
Winkeljohn, Victoria M.
Rotterman, Travis M.
Stolfi, Alberto
Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function
title Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function
title_full Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function
title_fullStr Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function
title_full_unstemmed Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function
title_short Using CRISPR/Cas9 to identify genes required for mechanosensory neuron development and function
title_sort using crispr/cas9 to identify genes required for mechanosensory neuron development and function
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197531/
https://www.ncbi.nlm.nih.gov/pubmed/37214826
http://dx.doi.org/10.1101/2023.05.08.539861
work_keys_str_mv AT johnsonchristopherj usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT kulkarniakhil usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT buxtonwilliamj usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT huitszy usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT kayasthaanusha usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT khojaalwina usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT leandrejoviane usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT mehtavanshikav usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT ostrowskilogan usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT pareizsericag usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT scottorebeccal usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT vargasvanesa usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT vellingiriraveenam usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT verzinogiulia usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT vohrarhea usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT wakadesaurabhc usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT winkeljohnveronicam usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT winkeljohnvictoriam usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT rottermantravism usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction
AT stolfialberto usingcrisprcas9toidentifygenesrequiredformechanosensoryneurondevelopmentandfunction