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A large-scale zebrafish gene knockout resource for the genome-wide study of gene function

With the completion of the zebrafish genome sequencing project, it becomes possible to analyze the function of zebrafish genes in a systematic way. The first step in such an analysis is to inactivate each protein-coding gene by targeted or random mutation. Here we describe a streamlined pipeline usi...

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Autores principales: Varshney, Gaurav K., Lu, Jing, Gildea, Derek E., Huang, Haigen, Pei, Wuhong, Yang, Zhongan, Huang, Sunny C., Schoenfeld, David, Pho, Nam H., Casero, David, Hirase, Takashi, Mosbrook-Davis, Deborah, Zhang, Suiyuan, Jao, Li-En, Zhang, Bo, Woods, Ian G., Zimmerman, Steven, Schier, Alexander F., Wolfsberg, Tyra G., Pellegrini, Matteo, Burgess, Shawn M., Lin, Shuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613589/
https://www.ncbi.nlm.nih.gov/pubmed/23382537
http://dx.doi.org/10.1101/gr.151464.112
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author Varshney, Gaurav K.
Lu, Jing
Gildea, Derek E.
Huang, Haigen
Pei, Wuhong
Yang, Zhongan
Huang, Sunny C.
Schoenfeld, David
Pho, Nam H.
Casero, David
Hirase, Takashi
Mosbrook-Davis, Deborah
Zhang, Suiyuan
Jao, Li-En
Zhang, Bo
Woods, Ian G.
Zimmerman, Steven
Schier, Alexander F.
Wolfsberg, Tyra G.
Pellegrini, Matteo
Burgess, Shawn M.
Lin, Shuo
author_facet Varshney, Gaurav K.
Lu, Jing
Gildea, Derek E.
Huang, Haigen
Pei, Wuhong
Yang, Zhongan
Huang, Sunny C.
Schoenfeld, David
Pho, Nam H.
Casero, David
Hirase, Takashi
Mosbrook-Davis, Deborah
Zhang, Suiyuan
Jao, Li-En
Zhang, Bo
Woods, Ian G.
Zimmerman, Steven
Schier, Alexander F.
Wolfsberg, Tyra G.
Pellegrini, Matteo
Burgess, Shawn M.
Lin, Shuo
author_sort Varshney, Gaurav K.
collection PubMed
description With the completion of the zebrafish genome sequencing project, it becomes possible to analyze the function of zebrafish genes in a systematic way. The first step in such an analysis is to inactivate each protein-coding gene by targeted or random mutation. Here we describe a streamlined pipeline using proviral insertions coupled with high-throughput sequencing and mapping technologies to widely mutagenize genes in the zebrafish genome. We also report the first 6144 mutagenized and archived F(1)'s predicted to carry up to 3776 mutations in annotated genes. Using in vitro fertilization, we have rescued and characterized ∼0.5% of the predicted mutations, showing mutation efficacy and a variety of phenotypes relevant to both developmental processes and human genetic diseases. Mutagenized fish lines are being made freely available to the public through the Zebrafish International Resource Center. These fish lines establish an important milestone for zebrafish genetics research and should greatly facilitate systematic functional studies of the vertebrate genome.
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spelling pubmed-36135892013-10-01 A large-scale zebrafish gene knockout resource for the genome-wide study of gene function Varshney, Gaurav K. Lu, Jing Gildea, Derek E. Huang, Haigen Pei, Wuhong Yang, Zhongan Huang, Sunny C. Schoenfeld, David Pho, Nam H. Casero, David Hirase, Takashi Mosbrook-Davis, Deborah Zhang, Suiyuan Jao, Li-En Zhang, Bo Woods, Ian G. Zimmerman, Steven Schier, Alexander F. Wolfsberg, Tyra G. Pellegrini, Matteo Burgess, Shawn M. Lin, Shuo Genome Res Resource With the completion of the zebrafish genome sequencing project, it becomes possible to analyze the function of zebrafish genes in a systematic way. The first step in such an analysis is to inactivate each protein-coding gene by targeted or random mutation. Here we describe a streamlined pipeline using proviral insertions coupled with high-throughput sequencing and mapping technologies to widely mutagenize genes in the zebrafish genome. We also report the first 6144 mutagenized and archived F(1)'s predicted to carry up to 3776 mutations in annotated genes. Using in vitro fertilization, we have rescued and characterized ∼0.5% of the predicted mutations, showing mutation efficacy and a variety of phenotypes relevant to both developmental processes and human genetic diseases. Mutagenized fish lines are being made freely available to the public through the Zebrafish International Resource Center. These fish lines establish an important milestone for zebrafish genetics research and should greatly facilitate systematic functional studies of the vertebrate genome. Cold Spring Harbor Laboratory Press 2013-04 /pmc/articles/PMC3613589/ /pubmed/23382537 http://dx.doi.org/10.1101/gr.151464.112 Text en © 2013, Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Resource
Varshney, Gaurav K.
Lu, Jing
Gildea, Derek E.
Huang, Haigen
Pei, Wuhong
Yang, Zhongan
Huang, Sunny C.
Schoenfeld, David
Pho, Nam H.
Casero, David
Hirase, Takashi
Mosbrook-Davis, Deborah
Zhang, Suiyuan
Jao, Li-En
Zhang, Bo
Woods, Ian G.
Zimmerman, Steven
Schier, Alexander F.
Wolfsberg, Tyra G.
Pellegrini, Matteo
Burgess, Shawn M.
Lin, Shuo
A large-scale zebrafish gene knockout resource for the genome-wide study of gene function
title A large-scale zebrafish gene knockout resource for the genome-wide study of gene function
title_full A large-scale zebrafish gene knockout resource for the genome-wide study of gene function
title_fullStr A large-scale zebrafish gene knockout resource for the genome-wide study of gene function
title_full_unstemmed A large-scale zebrafish gene knockout resource for the genome-wide study of gene function
title_short A large-scale zebrafish gene knockout resource for the genome-wide study of gene function
title_sort large-scale zebrafish gene knockout resource for the genome-wide study of gene function
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613589/
https://www.ncbi.nlm.nih.gov/pubmed/23382537
http://dx.doi.org/10.1101/gr.151464.112
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