Polyphosphate loss promotes SNF/SWI- and gcn5-dependent mitotic induction of PHO5

被引:66
作者
Neef, DW [1 ]
Kladde, MP [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
关键词
YEAST SACCHAROMYCES-CEREVISIAE; CELL-CYCLE; INORGANIC POLYPHOSPHATE; PHOSPHATE-METABOLISM; EXPRESSION ANALYSIS; GENE ACTIVATION; MESSENGER-RNA; CHROMATIN; COMPLEX; TRANSCRIPTION;
D O I
10.1128/MCB.23.11.3788-3797.2003
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
Approximately 800 transcripts in Saccharomyces cerevisiae are cell cycle regulated. The oscillation of similar to40% of these genes, including a prominent subclass involved in nutrient acquisition, is not understood. To address this problem, we focus on the mitosis-specific activation of the phosphate-responsive promoter, PHO5. We show that the unexpected mitotic induction of the PHO5 acid phosphatase in rich medium requires the transcriptional activators Pho4 and Pho2, the cyclin-dependent kinase inhibitor Pho81, and the chromatin-associated enzymes Gcn5 and Snf2/Swi2. PHO5 mitotic activation is repressed by addition of orthophosphate, which significantly increases cellular polyphosphate. Polyphosphate levels also fluctuate inversely with PHO5 mRNA during the cell cycle, further substantiating an antagonistic link between this phosphate polymer and PHO5 mitotic regulation. Moreover, deletion of PHM3, required for polyphosphate accumulation, leads to premature onset of PHO5 expression, as well as an increased rate, magnitude, and duration of PHO5 activation. Orthophosphate addition, however, represses mitotic PHO5 expression in a phm3Delta strain. Thus, polyphosphate per se is not necessary to repress PHO transcription but, when present, replenishes cellular phosphate during nutrient depletion. These results demonstrate a dynamic mechanism of mitotic transcriptional regulation that operates mostly independently of factors that drive progression through the cell cycle.
引用
收藏
页码:3788 / 3797
页数:10
相关论文
共 48 条
[1]   Increasing the rate of chromatin remodeling and gene activation -: a novel role for the histone acetyltransferase Gcn5 [J].
Barbaric, S ;
Walker, J ;
Schmid, A ;
Svejstrup, JQ ;
Hörz, W .
EMBO JOURNAL, 2001, 20 (17) :4944-4951
[2]  
Brachmann CB, 1998, YEAST, V14, P115
[3]   Tetrahymena histone acetyltransferase A: A homolog to yeast Gcn5p linking histone acetylation to gene activation [J].
Brownell, JE ;
Zhou, JX ;
Ranalli, T ;
Kobayashi, R ;
Edmondson, DG ;
Roth, SY ;
Allis, CD .
CELL, 1996, 84 (06) :843-851
[4]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[5]   ISOLATION OF INTACT CHAINS OF POLYPHOSPHATE FROM PROPIONIBACTERIUM-SHERMANII GROWN ON GLUCOSE OR LACTATE [J].
CLARK, JE ;
BEEGEN, H ;
WOOD, HG .
JOURNAL OF BACTERIOLOGY, 1986, 168 (03) :1212-1219
[6]   A novel family of yeast chaperons involved in the distribution of V-ATPase and other membrane proteins [J].
Cohen, A ;
Perzov, N ;
Nelson, H ;
Nelson, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :26885-26893
[7]   A POTENTIAL POSITIVE FEEDBACK LOOP CONTROLLING CLN1 AND CLN2 GENE-EXPRESSION AT THE START OF THE YEAST-CELL CYCLE [J].
CROSS, FR ;
TINKELENBERG, AH .
CELL, 1991, 65 (05) :875-883
[8]  
DUNN T, 1994, J BIOL CHEM, V269, P7273
[9]   DNA DAMAGE INDUCTION OF RIBONUCLEOTIDE REDUCTASE [J].
ELLEDGE, SJ ;
DAVIS, RW .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :4932-4940
[10]   RNA polymerase II holoenzyme recruitment is sufficient to remodel chromatin at the yeast PHO5 promoter [J].
Gaudreau, L ;
Schmid, A ;
Blaschke, D ;
Ptashne, M ;
Horz, W .
CELL, 1997, 89 (01) :55-62