Cargando…
The Xenopus ORFeome: A resource that enables functional genomics
Functional characterisation of proteins and large-scale, systems-level studies are enabled by extensive sets of cloned open reading frames (ORFs) in an easily-accessible format that enables many different applications. Here we report the release of the first stage of the Xenopus ORFeome, which conta...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684507/ https://www.ncbi.nlm.nih.gov/pubmed/26391338 http://dx.doi.org/10.1016/j.ydbio.2015.09.004 |
_version_ | 1782406192388112384 |
---|---|
author | Grant, Ian M. Balcha, Dawit Hao, Tong Shen, Yun Trivedi, Prasad Patrushev, Ilya Fortriede, Joshua D. Karpinka, John B. Liu, Limin Zorn, Aaron M. Stukenberg, P. Todd Hill, David E. Gilchrist, Michael J. |
author_facet | Grant, Ian M. Balcha, Dawit Hao, Tong Shen, Yun Trivedi, Prasad Patrushev, Ilya Fortriede, Joshua D. Karpinka, John B. Liu, Limin Zorn, Aaron M. Stukenberg, P. Todd Hill, David E. Gilchrist, Michael J. |
author_sort | Grant, Ian M. |
collection | PubMed |
description | Functional characterisation of proteins and large-scale, systems-level studies are enabled by extensive sets of cloned open reading frames (ORFs) in an easily-accessible format that enables many different applications. Here we report the release of the first stage of the Xenopus ORFeome, which contains 8673 ORFs from the Xenopus Gene Collection (XGC) for Xenopus laevis, cloned into a Gateway® donor vector enabling rapid in-frame transfer of the ORFs to expression vectors. This resource represents an estimated 7871 unique genes, approximately 40% of the non-redundant X. laevis gene complement, and includes 2724 genes where the human ortholog has an association with disease. Transfer into the Gateway system was validated by 5′ and 3′ end sequencing of the entire collection and protein expression of a set of test clones. In a parallel process, the underlying ORF predictions from the original XGC collection were re-analysed to verify quality and full-length status, identifying those proteins likely to exhibit truncations when translated. These data are integrated into Xenbase, the Xenopus community database, which associates genomic, expression, function and human disease model metadata to each ORF, enabling end-users to search for ORFeome clones with links to commercial distributors of the collection. When coupled with the experimental advantages of Xenopus eggs and embryos, the ORFeome collection represents a valuable resource for functional genomics and disease modelling. |
format | Online Article Text |
id | pubmed-4684507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-46845072016-03-24 The Xenopus ORFeome: A resource that enables functional genomics Grant, Ian M. Balcha, Dawit Hao, Tong Shen, Yun Trivedi, Prasad Patrushev, Ilya Fortriede, Joshua D. Karpinka, John B. Liu, Limin Zorn, Aaron M. Stukenberg, P. Todd Hill, David E. Gilchrist, Michael J. Dev Biol Article Functional characterisation of proteins and large-scale, systems-level studies are enabled by extensive sets of cloned open reading frames (ORFs) in an easily-accessible format that enables many different applications. Here we report the release of the first stage of the Xenopus ORFeome, which contains 8673 ORFs from the Xenopus Gene Collection (XGC) for Xenopus laevis, cloned into a Gateway® donor vector enabling rapid in-frame transfer of the ORFs to expression vectors. This resource represents an estimated 7871 unique genes, approximately 40% of the non-redundant X. laevis gene complement, and includes 2724 genes where the human ortholog has an association with disease. Transfer into the Gateway system was validated by 5′ and 3′ end sequencing of the entire collection and protein expression of a set of test clones. In a parallel process, the underlying ORF predictions from the original XGC collection were re-analysed to verify quality and full-length status, identifying those proteins likely to exhibit truncations when translated. These data are integrated into Xenbase, the Xenopus community database, which associates genomic, expression, function and human disease model metadata to each ORF, enabling end-users to search for ORFeome clones with links to commercial distributors of the collection. When coupled with the experimental advantages of Xenopus eggs and embryos, the ORFeome collection represents a valuable resource for functional genomics and disease modelling. Elsevier 2015-12-15 /pmc/articles/PMC4684507/ /pubmed/26391338 http://dx.doi.org/10.1016/j.ydbio.2015.09.004 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Grant, Ian M. Balcha, Dawit Hao, Tong Shen, Yun Trivedi, Prasad Patrushev, Ilya Fortriede, Joshua D. Karpinka, John B. Liu, Limin Zorn, Aaron M. Stukenberg, P. Todd Hill, David E. Gilchrist, Michael J. The Xenopus ORFeome: A resource that enables functional genomics |
title | The Xenopus ORFeome: A resource that enables functional genomics |
title_full | The Xenopus ORFeome: A resource that enables functional genomics |
title_fullStr | The Xenopus ORFeome: A resource that enables functional genomics |
title_full_unstemmed | The Xenopus ORFeome: A resource that enables functional genomics |
title_short | The Xenopus ORFeome: A resource that enables functional genomics |
title_sort | xenopus orfeome: a resource that enables functional genomics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684507/ https://www.ncbi.nlm.nih.gov/pubmed/26391338 http://dx.doi.org/10.1016/j.ydbio.2015.09.004 |
work_keys_str_mv | AT grantianm thexenopusorfeomearesourcethatenablesfunctionalgenomics AT balchadawit thexenopusorfeomearesourcethatenablesfunctionalgenomics AT haotong thexenopusorfeomearesourcethatenablesfunctionalgenomics AT shenyun thexenopusorfeomearesourcethatenablesfunctionalgenomics AT trivediprasad thexenopusorfeomearesourcethatenablesfunctionalgenomics AT patrushevilya thexenopusorfeomearesourcethatenablesfunctionalgenomics AT fortriedejoshuad thexenopusorfeomearesourcethatenablesfunctionalgenomics AT karpinkajohnb thexenopusorfeomearesourcethatenablesfunctionalgenomics AT liulimin thexenopusorfeomearesourcethatenablesfunctionalgenomics AT zornaaronm thexenopusorfeomearesourcethatenablesfunctionalgenomics AT stukenbergptodd thexenopusorfeomearesourcethatenablesfunctionalgenomics AT hilldavide thexenopusorfeomearesourcethatenablesfunctionalgenomics AT gilchristmichaelj thexenopusorfeomearesourcethatenablesfunctionalgenomics AT grantianm xenopusorfeomearesourcethatenablesfunctionalgenomics AT balchadawit xenopusorfeomearesourcethatenablesfunctionalgenomics AT haotong xenopusorfeomearesourcethatenablesfunctionalgenomics AT shenyun xenopusorfeomearesourcethatenablesfunctionalgenomics AT trivediprasad xenopusorfeomearesourcethatenablesfunctionalgenomics AT patrushevilya xenopusorfeomearesourcethatenablesfunctionalgenomics AT fortriedejoshuad xenopusorfeomearesourcethatenablesfunctionalgenomics AT karpinkajohnb xenopusorfeomearesourcethatenablesfunctionalgenomics AT liulimin xenopusorfeomearesourcethatenablesfunctionalgenomics AT zornaaronm xenopusorfeomearesourcethatenablesfunctionalgenomics AT stukenbergptodd xenopusorfeomearesourcethatenablesfunctionalgenomics AT hilldavide xenopusorfeomearesourcethatenablesfunctionalgenomics AT gilchristmichaelj xenopusorfeomearesourcethatenablesfunctionalgenomics |