Saccharomyces kluyveri as a model organism to study pyrimidine degradation

被引:12
作者
Beck, Halfdan [1 ]
Dobritzsch, Doreen [2 ]
Piskur, Jure [1 ]
机构
[1] Lund Univ, Dept Cell & Organism Biol, SE-22362 Lund, Sweden
[2] Karolinska Inst, Dept Med Biochem & Biophys, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
nonconventional yeast; structure-function relationship; nucleic acid precursors; pyrimidine; cancer;
D O I
10.1111/j.1567-1364.2008.00442.x
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
The yeast Saccharomyces kluyveri (Lachancea kluyveri), a far relative of Saccharomyces cerevisiae, is not a widely studied organism in the laboratory. However, significant contributions to the understanding of nucleic acid precursors degradation in eukaryotes have been made using this model organism. Here we review eukaryotic pyrimidine degradation with emphasis on the contributions made with S. kluyveri and how this increases our understanding of human disease. Additionally, we discuss the possibilities and limitations of this nonconventional yeast as a laboratory organism.
引用
收藏
页码:1209 / 1213
页数:5
相关论文
共 28 条
[1]   Dihydropyrimidine dehydrogenase deficiency presenting at birth [J].
Al-Sanna'a, NA ;
Van Kuilenburg, ABP ;
Atrak, TM ;
Jabbar, MAA ;
Van Gennip, AH .
JOURNAL OF INHERITED METABOLIC DISEASE, 2005, 28 (05) :793-796
[2]   A recruited protease is involved in catabolism of pyrimidines [J].
Andersen, Birgit ;
Lundgren, Stina ;
Dobritzsch, Doreen ;
Piskur, Jure .
JOURNAL OF MOLECULAR BIOLOGY, 2008, 379 (02) :243-250
[3]   Catabolism of pyrimidines in yeast:: A tool to understand degradation of anticancer drugs [J].
Andersen, G. ;
Merico, A. ;
Bjornberg, O. ;
Andersen, B. ;
Schnackerz, K. D. ;
Dobritzsch, D. ;
Piskur, J. ;
Compagno, C. .
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, 2006, 25 (9-11) :991-996
[4]   A second pathway to degrade pyrimidine nucleic acid precursors in eukaryotes [J].
Andersen, Gorm ;
Bjoernberg, Olof ;
Polakova, Silvia ;
Pynyaha, Yuriy ;
Rasmussen, Anna ;
Moller, Kasper ;
Hofer, Anders ;
Moritz, Thomas ;
Sandrini, Michael Paolo Bastner ;
Merico, Anna-Maria ;
Compagno, Concetta ;
Akerlund, Hans-Erik ;
Gojkovic, Zoran ;
Piskur, Jure .
JOURNAL OF MOLECULAR BIOLOGY, 2008, 380 (04) :656-666
[5]   A gene duplication led to specialized γ-aminobutyrate and β-alanine aminotransferase in yeast [J].
Andersen, Gorm ;
Andersen, Birgit ;
Dobritzsch, Doreen ;
Schnackerz, Klaus D. ;
Piskur, Jure .
FEBS JOURNAL, 2007, 274 (07) :1804-1817
[6]   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
[7]  
DeLano W. L., 2002, PYMOL
[8]   Dihydropyrimidine dehydrogenase deficiency and acute neurological presentation [J].
Fiumara, A ;
van Kuilenburg, ABP ;
Caruso, U ;
Nucifora, C ;
Marzullo, E ;
Barone, R ;
Meli, C ;
van Gennip, AH .
JOURNAL OF INHERITED METABOLIC DISEASE, 2003, 26 (04) :407-409
[9]   PYD2 encodes 5,6-dihydropyrimidine amidohydrolase, which participates in a novel fungal catabolic pathway [J].
Gojkovic, Z ;
Jahnke, K ;
Schnackerz, KD ;
Piskur, J .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 295 (04) :1073-1087
[10]   Horizontal gene transfer promoted evolution of the ability to propagate under anaerobic conditions in yeasts [J].
Gojkovic, Z ;
Knecht, W ;
Zameitat, E ;
Warneboldt, J ;
Coutelis, JB ;
Pynyaha, Y ;
Neuveglise, C ;
Moller, K ;
Löffler, M ;
Piskur, J .
MOLECULAR GENETICS AND GENOMICS, 2004, 271 (04) :387-393