A Biomedically Enriched Collection of 7000 Human ORF Clones

被引:19
作者
Rolfs, Andreas [1 ]
Hu, Yanhui [1 ]
Ebert, Lars [2 ]
Hoffmann, Dietmar [3 ]
Zuo, Dongmei [1 ]
Ramachandran, Niro [1 ]
Raphael, Jacob [1 ]
Kelley, Fontina [1 ]
McCarron, Seamus [1 ]
Jepson, Daniel A. [1 ]
Shen, Binghua [1 ]
Baqui, Munira M. A. [1 ]
Pearlberg, Joseph [1 ]
Taycher, Elena [1 ]
DeLoughery, Craig [3 ]
Hoerlein, Andreas [2 ]
Korn, Bernhard [2 ]
LaBaer, Joshua [1 ]
机构
[1] Harvard Univ, Sch Med, Harvard Inst Prote, Cambridge, MA 02138 USA
[2] RZPD, Heidelberg, Germany
[3] Sanofi Aventis, Cambridge, MA USA
关键词
D O I
10.1371/journal.pone.0001528
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report the production and availability of over 7000 fully sequence verified plasmid ORF clones representing over 3400 unique human genes. These ORF clones were derived using the human MGC collection as template and were produced in two formats: with and without stop codons. Thus, this collection supports the production of either native protein or proteins with fusion tags added to either or both ends. The template clones used to generate this collection were enriched in three ways. First, gene redundancy was removed. Second, clones were selected to represent the best available GenBank reference sequence. Finally, a literature-based software tool was used to evaluate the list of target genes to ensure that it broadly reflected biomedical research interests. The target gene list was compared with 4000 human diseases and over 8500 biological and chemical MeSH classes in,15 Million publications recorded in PubMed at the time of analysis. The outcome of this analysis revealed that relative to the genome and the MGC collection, this collection is enriched for the presence of genes with published associations with a wide range of diseases and biomedical terms without displaying a particular bias towards any single disease or concept. Thus, this collection is likely to be a powerful resource for researchers who wish to study protein function in a set of genes with documented biomedical significance.
引用
收藏
页数:8
相关论文
共 24 条
[1]   Systematic recovery and analysis of full-ORF human cDNA clones [J].
Baross, A ;
Butterfield, YSN ;
Coughlin, SM ;
Zeng, T ;
Griffith, M ;
Griffith, OL ;
Petrescu, AS ;
Smailus, DE ;
Khattra, J ;
McDonald, HL ;
McKay, SJ ;
Moksa, M ;
Holt, RA ;
Marra, MA .
GENOME RESEARCH, 2004, 14 (10B) :2083-2092
[2]   A genome annotation-driven approach to cloning the human ORFeome [J].
Collins, JE ;
Wright, C ;
Edwards, CA ;
Davis, MP ;
Grinham, JA ;
Cole, CG ;
Goward, ME ;
Aguado, B ;
Mallya, M ;
Mokrab, Y ;
Huckle, EJ ;
Beare, DM ;
Dunham, I .
GENOME BIOLOGY, 2004, 5 (10)
[3]   Functional dynamics of PDZ binding domains: A normal-mode analysis [J].
De Los Rios, P ;
Cecconi, F ;
Pretre, A ;
Dietler, G ;
Michielin, O ;
Piazza, F ;
Juanico, B .
BIOPHYSICAL JOURNAL, 2005, 89 (01) :14-21
[4]  
Gerhard DS, 2004, GENOME RES, V14, P2121, DOI 10.1101/gr.2596504
[5]   Primer design for large scale sequencing [J].
Haas, S ;
Vingron, M ;
Poustka, A ;
Wiemann, S .
NUCLEIC ACIDS RESEARCH, 1998, 26 (12) :3006-3012
[6]   Cadherin adhesion depends on a salt bridge at the N-terminus [J].
Harrison, OJ ;
Corps, EM ;
Kilshaw, PJ .
JOURNAL OF CELL SCIENCE, 2005, 118 (18) :4123-4130
[7]   The surprising complexity of signal sequences [J].
Hegde, Ramanujan S. ;
Bernstein, Harris D. .
TRENDS IN BIOCHEMICAL SCIENCES, 2006, 31 (10) :563-571
[8]   Approaching a complete repository of sequence-verified protein-encoding clones for Saccharomyces cerevisiae [J].
Hu, Yanhui ;
Rolfs, Andreas ;
Bhullar, Bhupinder ;
Murthy, Tellamraju V. S. ;
Zhu, Cong ;
Berger, Michael F. ;
Camargo, Anamaria A. ;
Kelley, Fontina ;
McCarron, Seamus ;
Jepson, Daniel ;
Richardson, Aaron ;
Raphael, Jacob ;
Moreira, Donna ;
Taycher, Elena ;
Zuo, Dongmei ;
Mohr, Stephanie ;
Kane, Michael F. ;
Williamson, Janice ;
Simpson, Andrew ;
Bulyk, Martha L. ;
Harlow, Edward ;
Marsischky, Gerald ;
Kolodner, Richard D. ;
LaBaer, Joshua .
GENOME RESEARCH, 2007, 17 (04) :536-543
[9]   Analysis of genomic and proteomic data using advanced literature mining [J].
Hu, YH ;
Hines, LM ;
Weng, HF ;
Zuo, DM ;
Rivera, M ;
Richardson, A ;
LaBaer, J .
JOURNAL OF PROTEOME RESEARCH, 2003, 2 (04) :405-412
[10]   h0RFeome v3.1: A resource of human open reading frames representing over 10,000 human genes [J].
Lamesch, Philippe ;
Li, Ning ;
Milstein, Stuart ;
Fan, Changyu ;
Hao, Tong ;
Szabo, Gabor ;
Hu, Zhenjun ;
Venkatesan, Kavitha ;
Bethel, Graeme ;
Martin, Paul ;
Rogers, Jane ;
Lawlor, Stephanie ;
McLaren, Stuart ;
Dricot, Amelie ;
Borick, Heather ;
Cusick, Michael E. ;
Vandenhaute, Jean ;
Dunham, Ian ;
Hill, David E. ;
Vidal, Marc .
GENOMICS, 2007, 89 (03) :307-315