Patterns of polymorphism and divergence in stress-related yeast proteins

被引:15
作者
Bowen, S
Roberts, C
Wheals, AE [1 ]
机构
[1] Univ Bath, Dept Biol & Biochem, Bath BA2 7AY, Avon, England
[2] Univ Leicester, Dept Genet, Leicester LE1 7RH, Leics, England
关键词
polymorphism; stress response; yeast; serine threonine regions; mutagenesis; adaptation; functional analysis; variable number tandem repeats;
D O I
10.1002/yea.1240
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
Yeast genomes contain variable number tandem repeats (VNTRs) within coding regions of DNA. A significant number of these genes are involved in cell rescue, defence and virulence and are regulated by genetic elements associated with stress. Alleles that encode variable length, single amino acid tracts, are mainly associated with transcription and proteins localized within the nucleus. Alleles that encode proteins containing oligopeptide repeats or minisatellites are over-represented in cell wall and extracellular space locations. Functional analysis of the latter group reveals that these proteins are involved in biogenesis of cellular components and in interaction with the cellular environment, especially in relation to stress resistance, heat shock response, temperature perception and adhesion. A significantly high number of these proteins have regions rich in threonine and/or serine that contain repeated sequences, variable in length within yeast species. DNA sequences encoding serine- and/or threonine-rich regions give rise to polymorphic alleles and therefore may confer a selective advantage to cells. We propose that these regions are the focus of mutational and recombination events that, when coupled with directed selection, may contribute to genetic variation within stress-related genes. Copyright (c) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:659 / 668
页数:10
相关论文
共 56 条
[1]   Amino acid reiterations in yeast are overrepresented in particular classes of proteins and show evidence of a slippage-like mutational process [J].
Albà, MM ;
Santibàñez-Koref, MF ;
Hancock, JM .
JOURNAL OF MOLECULAR EVOLUTION, 1999, 49 (06) :789-797
[2]   Detecting cryptically simple protein sequences using the SIMPLE algorithm [J].
Albà, MM ;
Laskowski, RA ;
Hancock, JM .
BIOINFORMATICS, 2002, 18 (05) :672-678
[3]  
ALBA MM, 2001, MOL BIOL EVOL, V18, P1014
[4]  
ASHLEY CT, 1995, NAT GENET, V13, P390
[5]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[6]   Tandem repeats finder: a program to analyze DNA sequences [J].
Benson, G .
NUCLEIC ACIDS RESEARCH, 1999, 27 (02) :573-580
[7]  
Bishop AJR, 2000, GENETICS, V156, P7
[8]   Oxidative stress inactivates the human DNA mismatch repair system [J].
Chang, CL ;
Marra, G ;
Chauhan, DP ;
Ha, HT ;
Chang, DK ;
Ricciardiello, L ;
Randolph, A ;
Carethers, JM ;
Boland, CR .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 283 (01) :C148-C154
[9]   Finding functional features in Saccharomyces genomes by phylogenetic footprinting [J].
Cliften, P ;
Sudarsanam, P ;
Desikan, A ;
Fulton, L ;
Fulton, B ;
Majors, J ;
Waterston, R ;
Cohen, BA ;
Johnston, M .
SCIENCE, 2003, 301 (5629) :71-76
[10]  
DEGROOT PW, 2003, YEAST, V13, P1477