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Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy

The arrival of simple and reliable methods for 3D imaging of mouse embryos has opened the possibility of analysing normal and abnormal development in a far more systematic and comprehensive manner than has hitherto been possible. This will not only help to extend our understanding of normal tissue a...

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Detalles Bibliográficos
Autores principales: Weninger, Wolfgang J., Geyer, Stefan H., Martineau, Alexandrine, Galli, Antonella, Adams, David J., Wilson, Robert, Mohun, Timothy J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Limited 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174525/
https://www.ncbi.nlm.nih.gov/pubmed/25256713
http://dx.doi.org/10.1242/dmm.016337
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author Weninger, Wolfgang J.
Geyer, Stefan H.
Martineau, Alexandrine
Galli, Antonella
Adams, David J.
Wilson, Robert
Mohun, Timothy J.
author_facet Weninger, Wolfgang J.
Geyer, Stefan H.
Martineau, Alexandrine
Galli, Antonella
Adams, David J.
Wilson, Robert
Mohun, Timothy J.
author_sort Weninger, Wolfgang J.
collection PubMed
description The arrival of simple and reliable methods for 3D imaging of mouse embryos has opened the possibility of analysing normal and abnormal development in a far more systematic and comprehensive manner than has hitherto been possible. This will not only help to extend our understanding of normal tissue and organ development but, by applying the same approach to embryos from genetically modified mouse lines, such imaging studies could also transform our knowledge of gene function in embryogenesis and the aetiology of developmental disorders. The International Mouse Phenotyping Consortium is coordinating efforts to phenotype single gene knockouts covering the entire mouse genome, including characterising developmental defects for those knockout lines that prove to be embryonic lethal. Here, we present a pilot study of 34 such lines, utilising high-resolution episcopic microscopy (HREM) for comprehensive 2D and 3D imaging of homozygous null embryos and their wild-type littermates. We present a simple phenotyping protocol that has been developed to take advantage of the high-resolution images obtained by HREM and that can be used to score tissue and organ abnormalities in a reliable manner. Using this approach with embryos at embryonic day 14.5, we show the wide range of structural abnormalities that are likely to be detected in such studies and the variability in phenotypes between sibling homozygous null embryos.
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spelling pubmed-41745252014-10-16 Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy Weninger, Wolfgang J. Geyer, Stefan H. Martineau, Alexandrine Galli, Antonella Adams, David J. Wilson, Robert Mohun, Timothy J. Dis Model Mech Research Article The arrival of simple and reliable methods for 3D imaging of mouse embryos has opened the possibility of analysing normal and abnormal development in a far more systematic and comprehensive manner than has hitherto been possible. This will not only help to extend our understanding of normal tissue and organ development but, by applying the same approach to embryos from genetically modified mouse lines, such imaging studies could also transform our knowledge of gene function in embryogenesis and the aetiology of developmental disorders. The International Mouse Phenotyping Consortium is coordinating efforts to phenotype single gene knockouts covering the entire mouse genome, including characterising developmental defects for those knockout lines that prove to be embryonic lethal. Here, we present a pilot study of 34 such lines, utilising high-resolution episcopic microscopy (HREM) for comprehensive 2D and 3D imaging of homozygous null embryos and their wild-type littermates. We present a simple phenotyping protocol that has been developed to take advantage of the high-resolution images obtained by HREM and that can be used to score tissue and organ abnormalities in a reliable manner. Using this approach with embryos at embryonic day 14.5, we show the wide range of structural abnormalities that are likely to be detected in such studies and the variability in phenotypes between sibling homozygous null embryos. The Company of Biologists Limited 2014-10 /pmc/articles/PMC4174525/ /pubmed/25256713 http://dx.doi.org/10.1242/dmm.016337 Text en © 2014. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Weninger, Wolfgang J.
Geyer, Stefan H.
Martineau, Alexandrine
Galli, Antonella
Adams, David J.
Wilson, Robert
Mohun, Timothy J.
Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
title Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
title_full Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
title_fullStr Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
title_full_unstemmed Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
title_short Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
title_sort phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174525/
https://www.ncbi.nlm.nih.gov/pubmed/25256713
http://dx.doi.org/10.1242/dmm.016337
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