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From expression cloning to gene modeling: The development of Xenopus gene sequence resources
The Xenopus community has made concerted efforts over the last 10–12 years systematically to improve the available sequence information for this amphibian model organism ideally suited to the study of early development in vertebrates. Here I review progress in the collection of both sequence data an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wiley Subscription Services, Inc., A Wiley Company
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488295/ https://www.ncbi.nlm.nih.gov/pubmed/22344767 http://dx.doi.org/10.1002/dvg.22008 |
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author | Gilchrist, Michael J |
author_facet | Gilchrist, Michael J |
author_sort | Gilchrist, Michael J |
collection | PubMed |
description | The Xenopus community has made concerted efforts over the last 10–12 years systematically to improve the available sequence information for this amphibian model organism ideally suited to the study of early development in vertebrates. Here I review progress in the collection of both sequence data and physical clone reagents for protein coding genes. I conclude that we have cDNA sequences for around 50% and full-length clones for about 35% of the genes in Xenopus tropicalis, and similar numbers but a smaller proportion for Xenopus laevis. In addition, I demonstrate that the gaps in the current genome assembly create problems for the computational elucidation of gene sequences, and suggest some ways to ameliorate the effects of this. genesis 50:143–154, 2012. © 2012 Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-3488295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Wiley Subscription Services, Inc., A Wiley Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-34882952012-11-05 From expression cloning to gene modeling: The development of Xenopus gene sequence resources Gilchrist, Michael J Genesis Reviews The Xenopus community has made concerted efforts over the last 10–12 years systematically to improve the available sequence information for this amphibian model organism ideally suited to the study of early development in vertebrates. Here I review progress in the collection of both sequence data and physical clone reagents for protein coding genes. I conclude that we have cDNA sequences for around 50% and full-length clones for about 35% of the genes in Xenopus tropicalis, and similar numbers but a smaller proportion for Xenopus laevis. In addition, I demonstrate that the gaps in the current genome assembly create problems for the computational elucidation of gene sequences, and suggest some ways to ameliorate the effects of this. genesis 50:143–154, 2012. © 2012 Wiley Periodicals, Inc. Wiley Subscription Services, Inc., A Wiley Company 2012-03 2012-02-16 /pmc/articles/PMC3488295/ /pubmed/22344767 http://dx.doi.org/10.1002/dvg.22008 Text en Copyright © 2012 Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Terms and Conditions set out at http://wileyonlinelibrary.com/onlineopen#OnlineOpen_Terms |
spellingShingle | Reviews Gilchrist, Michael J From expression cloning to gene modeling: The development of Xenopus gene sequence resources |
title | From expression cloning to gene modeling: The development of Xenopus gene sequence resources |
title_full | From expression cloning to gene modeling: The development of Xenopus gene sequence resources |
title_fullStr | From expression cloning to gene modeling: The development of Xenopus gene sequence resources |
title_full_unstemmed | From expression cloning to gene modeling: The development of Xenopus gene sequence resources |
title_short | From expression cloning to gene modeling: The development of Xenopus gene sequence resources |
title_sort | from expression cloning to gene modeling: the development of xenopus gene sequence resources |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488295/ https://www.ncbi.nlm.nih.gov/pubmed/22344767 http://dx.doi.org/10.1002/dvg.22008 |
work_keys_str_mv | AT gilchristmichaelj fromexpressioncloningtogenemodelingthedevelopmentofxenopusgenesequenceresources |