Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region

被引:87
作者
Lehner, B [1 ]
Semple, JI [1 ]
Brown, SE [1 ]
Counsell, D [1 ]
Campbell, RD [1 ]
Sanderson, CM [1 ]
机构
[1] MRC, Rosalind Franklin Ctr Genom Res, Funct Genom Grp, Cambridge CB10 1SB, England
关键词
protein-protein interaction; yeast two-hybrid; human MHC class III region;
D O I
10.1016/S0888-7543(03)00235-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
High-throughput (HTP) protein-interaction assays, such as the yeast two-hybrid (Y2H) system, are enormously useful in predicting the functions of novel gene-products. HTP-Y2H screens typically do not include all of the reconfirmation and specificity tests used in small-scale studies, but the effects of omitting these steps have not been assessed. We performed HTP-Y2H screens that included all standard controls, using the predicted intracellular proteins expressed from the human MHC class III region, a region of the genome associated with many autoimmune diseases. The 91 novel interactions identified provide insight into the potential functions of many MHC genes, including C6orf47, LSM2, NELF-E (RDBP), DOM3Z, STK19, PBX2, RNF5, UAP56 (BAT1), ATP6G2, LST1/f, BAT2, Scythe (BAT3), CSNK2B, BAT5, and CLIC1. Surprisingly, our results predict that 1/3 of the proteins may have a role in mRNA processing, which suggests clustering of functionally related genes within the human genome. Most importantly, our analysis shows that omitting standard controls in HTP-Y2H screens could significantly compromise data quality. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:153 / 167
页数:15
相关论文
共 80 条
[1]   The Sm domain is an ancient RNA-binding motif with oligo(U) specificity [J].
Achsel, T ;
Stark, H ;
Lührmann, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (07) :3685-3689
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   Comparative genomics and evolution of proteins involved in RNA metabolism [J].
Anantharaman, V ;
Koonin, EV ;
Aravind, L .
NUCLEIC ACIDS RESEARCH, 2002, 30 (07) :1427-1464
[4]   The RNA processing exosome is linked to elongating RNA polymerase II in Drosophila [J].
Andrulis, ED ;
Werner, J ;
Nazarian, A ;
Erdjument-Bromage, H ;
Tempst, P ;
Lis, JT .
NATURE, 2002, 420 (6917) :837-841
[5]  
BADER GD, NUCL ACIDS RES, V31, P24803
[6]   Complete sequence and gene map of a human major histocompatibility complex [J].
Beck, S ;
Geraghty, D ;
Inoko, H ;
Rowen, L ;
Aguado, B ;
Bahram, S ;
Campbell, RD ;
Forbes, SA ;
Guillaudeux, T ;
Hood, L ;
Horton, R ;
Janer, M ;
Jasoni, C ;
Madan, A ;
Milne, S ;
Neville, M ;
Oka, A ;
Qin, S ;
Ribas-Despuig, G ;
Rogers, J ;
Shiina, T ;
Spies, T ;
Tamiya, G ;
Tashiro, H ;
Trowsdale, J ;
Vu, Q ;
Williams, L ;
Yamazaki, M .
NATURE, 1999, 401 (6756) :921-923
[7]   ASSEMBLY OF A PROCESSIVE MESSENGER-RNA POLYADENYLATION COMPLEX [J].
BIENROTH, S ;
KELLER, W ;
WAHLE, E .
EMBO JOURNAL, 1993, 12 (02) :585-594
[8]  
Brown MA, 1998, ARTHRITIS RHEUM, V41, P588, DOI 10.1002/1529-0131(199804)41:4<588::AID-ART5>3.3.CO
[9]  
2-S
[10]   From UBA to UBX: new words in the ubiquitin vocabulary [J].
Buchberger, A .
TRENDS IN CELL BIOLOGY, 2002, 12 (05) :216-221