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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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