The Xenopus ORFeome: A resource that enables functional genomics

被引:23
|
作者
Grant, Ian M. [1 ]
Balcha, Dawit [2 ,3 ]
Hao, Tong [2 ,3 ]
Shen, Yun [2 ,3 ]
Trivedi, Prasad [6 ]
Patrushev, Ilya [1 ]
Fortriede, Joshua D. [4 ]
Karpinka, John B. [5 ]
Liu, Limin [6 ]
Zorn, Aaron M. [4 ]
Stukenberg, P. Todd [6 ]
Hill, David E. [2 ,3 ]
Gilchrist, Michael J. [1 ]
机构
[1] Francis Crick Inst, Mill Hill Lab, London NW7 1AA, England
[2] Dana Farber Canc Inst, CCSB, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[4] Cincinnati Childrens Hosp Med Ctr, Div Dev Biol, Xenbase, Cincinnati, OH 45229 USA
[5] Univ Calgary, Dept Biol Sci, Xenbase, Calgary, AB, Canada
[6] Univ Virginia, Sch Med, Charlottesville, VA 22908 USA
基金
英国惠康基金; 英国医学研究理事会;
关键词
Gateway; Recombinational cloning; ORFeome; Xenopus; Open reading frame; Gene annotation; OPEN READING FRAMES; GENE COLLECTION; SYSTEMATIC IDENTIFICATION; EXPRESSION CLONING; VERSION; 1.1; LAEVIS; CHROMOSOMES; INHIBITOR; PROTEOME; PLATFORM;
D O I
10.1016/j.ydbio.2015.09.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 Xeno pus Gene Collection (XGC) for Xenopus laevis, cloned into a Gateway (R) 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. (C) 2015 The Authors. Published by Elsevier Inc.
引用
收藏
页码:345 / 357
页数:13
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