From gene to screen with yeast

被引:39
作者
Oliver, SG
机构
[1] Dept. Biochem. Appl. Molec. Biol., Univ. Manchester Inst. Sci. Technol., Manchester M60 1QD
基金
英国惠康基金;
关键词
D O I
10.1016/S0959-437X(97)80156-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
With the complete sequence now available, the yeast genome project enters a post-sequencing phase that will concentrate on a comprehensive determination of gene function. Novel techniques have been developed to undertake genome-wide functional analysis at the levels of phenotype, transcript and protein. These include techniques for the efficient deletion of individual genes while tagging the deletants with specific oligonucleotide signatures, as well as strategies to quantify the physiological effects of such deletions by comparing growth rates and metabolite profiles under a range of conditions. Comprehensive approaches to the study of gene expression include hybridization array technology to identify and quantify transcripts, and the exploitation of mass spectometry to identify proteins resolved by two-dimensional gel electrophoresis. Yeast presents opportunities for the discovery of new human medicines both via the recognition of functional homologies between human and yeast genes and by the use of yeast to express human coding sequences specifying potential drug targets.
引用
收藏
页码:405 / 409
页数:5
相关论文
共 49 条
[31]   Parallel human genome analysis: Microarray-based expression monitoring of 1000 genes [J].
Schena, M ;
Shalon, D ;
Heller, R ;
Chai, A ;
Brown, PO ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :10614-10619
[32]   CLONING OF 3 HUMAN MULTIFUNCTIONAL DENOVO PURINE BIOSYNTHETIC GENES BY FUNCTIONAL COMPLEMENTATION OF YEAST MUTATIONS [J].
SCHILD, D ;
BRAKE, AJ ;
KIEFER, MC ;
YOUNG, D ;
BARR, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) :2916-2920
[33]   Linking genome and proteome by mass spectrometry: Large-scale identification of yeast proteins from two dimensional gels [J].
Shevchenko, A ;
Jensen, ON ;
Podtelejnikov, AV ;
Sagliocco, F ;
Wilm, M ;
Vorm, O ;
Mortensen, P ;
Shevchenko, A ;
Boucherie, H ;
Mann, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14440-14445
[34]   Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar-coding strategy [J].
Shoemaker, DD ;
Lashkari, DA ;
Morris, D ;
Mittmann, M ;
Davis, RW .
NATURE GENETICS, 1996, 14 (04) :450-456
[35]   GENETIC FOOTPRINTING - A GENOMIC STRATEGY FOR DETERMINING A GENES FUNCTION GIVEN ITS SEQUENCE [J].
SMITH, V ;
BOTSTEIN, D ;
BROWN, PO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) :6479-6483
[36]   Functional analysis of the genes of yeast chromosome V by genetic footprinting [J].
Smith, V ;
Chou, KN ;
Lashkari, D ;
Botstein, D ;
Brown, PO .
SCIENCE, 1996, 274 (5295) :2069-2074
[37]   Review: Compilation and characteristics of dedicated transcription factors in Saccharomyces cerevisiae [J].
Svetlov, VV ;
Cooper, TG .
YEAST, 1995, 11 (15) :1439-1484
[38]  
TEUSINK B, 1997, METHODS MICROBIOLOGY
[39]  
THON VJ, 1993, J BIOL CHEM, V268, P7509
[40]   SERIAL ANALYSIS OF GENE-EXPRESSION [J].
VELCULESCU, VE ;
ZHANG, L ;
VOGELSTEIN, B ;
KINZLER, KW .
SCIENCE, 1995, 270 (5235) :484-487