Sulfur Metabolism Actively Promotes Initiation of Cell Division in Yeast

被引:17
作者
Blank, Heidi M. [1 ]
Gajjar, Shefali [1 ]
Belyanin, Andrey [1 ]
Polymenis, Michael [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
基金
美国国家科学基金会;
关键词
CYSTATHIONINE BETA-SYNTHASE; MITOCHONDRIAL PROTEIN ABF2P; SACCHAROMYCES-CEREVISIAE; DNA-REPLICATION; AMINO-ACIDS; CYCLE; DYSFUNCTION; MECHANISM; GENOME; MUTATIONS;
D O I
10.1371/journal.pone.0008018
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Background: Sulfur metabolism is required for initiation of cell division, but whether or not it can actively promote cell division remains unknown. Methodology/Principal Findings: Here we show that yeast cells with more mtDNA have an expanded reductive phase of their metabolic cycle and an increased sulfur metabolic flux. We also show that in wild type cells manipulations of sulfur metabolic flux phenocopy the enhanced growth rate of cells with more mtDNA. Furthermore, introduction of a hyperactive cystathionine-beta-synthase (CBS) allele in wild type cells accelerates initiation of DNA replication. Conclusions/Significance: Our results reveal a novel connection between a key sulfur metabolic enzyme, CBS, and the cell cycle. Since the analogous hyperactive CBS allele in human CBS suppresses other disease-causing CBS mutations, our findings may be relevant for human pathology. Taken together, our results demonstrate the importance of sulfur metabolism in actively promoting initiation of cell division.
引用
收藏
页数:7
相关论文
共 41 条
[1]
[Anonymous], 1994, METHODS YEAST GENETI
[2]
Reaction mechanism and regulation of cystathionine β-synthase [J].
Banerjee, R ;
Evande, R ;
Kabil, Ö ;
Ojha, S ;
Taoka, S .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2003, 1647 (1-2) :30-35
[3]
Kinetic characterization of recombinant human cystathionine β-synthase purified from E. coli [J].
Belew, Muluken S. ;
Quazi, Faraz I. ;
Willmore, William G. ;
Aitken, Susan M. .
PROTEIN EXPRESSION AND PURIFICATION, 2009, 64 (02) :139-145
[4]
Inhibition of silencing and accelerated aging by nicotinamide, a putative negative regulator of yeast Sir2 and human SIRT1 [J].
Bitterman, KJ ;
Anderson, RM ;
Cohen, HY ;
Latorre-Esteves, M ;
Sinclair, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (47) :45099-45107
[5]
An increase in mitochondrial DNA promotes nuclear DNA replication in yeast [J].
Blank, Heidi M. ;
Li, Chonghua ;
Mueller, John E. ;
Bogomolnaya, Lydia M. ;
Bryk, Mary ;
Polymenis, Michael .
PLOS GENETICS, 2008, 4 (04)
[6]
Brosnan JT, 2006, J NUTR, V136, p1636S, DOI 10.1093/jn/136.6.1636S
[7]
Castrillo Juan I, 2007, J Biol, V6, P4, DOI 10.1186/jbiol54
[8]
Restriction of DNA replication to the reductive phase of the metabolic cycle protects genome integrity [J].
Chen, Zheng ;
Odstrcil, Elizabeth A. ;
Tu, Benjamin P. ;
McKnight, Steven L. .
SCIENCE, 2007, 316 (5833) :1916-1919
[9]
Genome-wide responses to mitochondrial dysfunction [J].
Epstein, CB ;
Waddle, JA ;
Hale, W ;
Davé, V ;
Thornton, J ;
Macatee, TL ;
Garner, HR ;
Butow, RA .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (02) :297-308
[10]
Sulfur sparing in the yeast proteome in response to sulfur demand [J].
Fauchon, M ;
Lagniel, G ;
Aude, JC ;
Lombardia, L ;
Soularue, P ;
Petat, C ;
Marguerie, G ;
Sentenac, A ;
Werner, M ;
Labarre, J .
MOLECULAR CELL, 2002, 9 (04) :713-723