Systematic hybrid LOH: a new method to reduce false positives and negatives during screening of yeast gene deletion libraries

被引:25
作者
Alvaro, David
Sunjevaric, Ivana
Reid, Robert J. D.
Lisby, Michael
Stillman, David J.
Rothstein, Rodney
机构
[1] Columbia Univ, Med Ctr, Dept Genet & Dev, New York, NY 10032 USA
[2] Univ Copenhagen, Dept Genet, Inst Mol Biol & Physiol, DK-1353 Copenhagen, Denmark
[3] Univ Utah, Hlth Sci Ctr, Dept Pathol, Salt Lake City, UT 84132 USA
关键词
deletion library; loss of heterozygosity; homologous recombination; hybrid;
D O I
10.1002/yea.1423
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a new method, systematic hybrid loss of heterozygosity, to facilitate genomic screens utilizing the yeast gene deletion library. Screening is performed using hybrid diploid strains produced through mating the library haploids with strains from a different genetic background, to minimize the contribution of unpredicted recessive genetic factors present in the individual library strains. We utilize a set of strains where each contains a conditional centromere construct on one of the 16 yeast chromosomes that allows the destabilization and selectable loss of that chromosome. After mating a library gene deletion haploid to such a conditional centromere strain, which corresponds to the chromosome carrying the gene deletion, loss of heterozygosity (LOH) at the gene deletion locus can be generated in these otherwise hybrid diploids. The use of hybrid diploid strains permits complementation of any spurious recessive mutations in the library strain, facilitating attribution of the observed phenotype to the documented gene deletion and dramatically reducing false positive results commonly obtained in library screens. The systematic hybrid LOH method can be applied to virtually any screen utilizing the yeast non-essential gene deletion library and is particularly useful for screens requiring the introduction of a genetic assay into the library strains. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:1097 / 1106
页数:10
相关论文
共 17 条
[1]  
Brachmann CB, 1998, YEAST, V14, P115
[2]   A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage [J].
Chang, M ;
Bellaoui, M ;
Boone, C ;
Brown, GW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (26) :16934-16939
[3]   Chemogenomic profiling: Identifying the functional interactions of small molecules in yeast [J].
Giaever, G ;
Flaherty, P ;
Kumm, J ;
Proctor, M ;
Nislow, C ;
Jaramillo, DF ;
Chu, AM ;
Jordan, MI ;
Arkin, AP ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (03) :793-798
[4]   The complete set of predicted genes from Saccharomyces cerevisiae in a readily usable form [J].
Hudson, JR ;
Dawson, EP ;
Rushing, KL ;
Jackson, CH ;
Lockshon, D ;
Conover, D ;
Lanciault, C ;
Harris, JR ;
Simmons, SJ ;
Rothstein, R ;
Fields, S .
GENOME RESEARCH, 1997, 7 (12) :1169-1173
[5]   Widespread aneuploidy revealed by DNA microarray expression profiling [J].
Hughes, TR ;
Roberts, CJ ;
Dai, HY ;
Jones, AR ;
Meyer, MR ;
Slade, D ;
Burchard, J ;
Dow, S ;
Ward, TR ;
Kidd, MJ ;
Friend, SH ;
Marton, MJ .
NATURE GENETICS, 2000, 25 (03) :333-337
[6]   Choreography of the DNA damage response: Spatiotemporal relationships among checkpoint and repair proteins [J].
Lisby, M ;
Barlow, JH ;
Burgess, RC ;
Rothstein, R .
CELL, 2004, 118 (06) :699-713
[7]   Rad52 forms DMA repair and recombination centers during S phase [J].
Lisby, M ;
Rothstein, R ;
Mortensen, UH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8276-8282
[8]   Cell Cycle-Regulated Centers of DNA Double-Strand Break Repair [J].
Lisby, Michael ;
de Mayolo, Adriana Antunez ;
Mortensen, Uffe H. ;
Rothstein, Rodney .
CELL CYCLE, 2003, 2 (05) :479-483
[9]   Discovering modes of action for therapeutic compounds using a genome-wide screen of yeast heterozygotes [J].
Lum, PY ;
Armour, CD ;
Stepaniants, SB ;
Cavet, G ;
Wolf, MK ;
Butler, JS ;
Hinshaw, JC ;
Garnier, P ;
Prestwich, GD ;
Leonardson, A ;
Garrett-Engele, P ;
Rush, CM ;
Bard, M ;
Schimmack, G ;
Phillips, JW ;
Roberts, CJ ;
Shoemaker, DD .
CELL, 2004, 116 (01) :121-137
[10]   Integration of chemical-genetic and genetic interaction data links bioactive compounds to cellular target pathways [J].
Parsons, AB ;
Brost, RL ;
Ding, HM ;
Li, ZJ ;
Zhang, CY ;
Sheikh, B ;
Brown, GW ;
Kane, PM ;
Hughes, TR ;
Boone, C .
NATURE BIOTECHNOLOGY, 2004, 22 (01) :62-69