Budding Yeast Escape Commitment to the Phosphate Starvation Program Using Gene Expression Noise

被引:27
作者
Vardi, Noam [1 ]
Levy, Sagi [1 ]
Assaf, Michael [2 ]
Carmi, Miri [1 ]
Barkai, Naama [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-7610001 Rehovot, Israel
[2] Hebrew Univ Jerusalem, Racah Inst Phys, IL-91904 Jerusalem, Israel
关键词
SACCHAROMYCES-CEREVISIAE; PATHWAY; SYSTEM; TRANSPORTERS; VARIABILITY; NETWORKS; CYCLE;
D O I
10.1016/j.cub.2013.08.043
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
Cells must rapidly adapt to changes in nutrient availability. In budding yeast, limitation of phosphate rapidly induces the expression of the Pho regulon genes [1-4]. This starvation program depends on the transcription factor Pho4, which translocates to the nucleus within minutes when cells are transferred to a low-phosphate medium [5]. Contrasting its rapid induction, we report that the Pho regulon can remain induced for dozens of generations in cells transferred back to high phosphate levels. For example, about 40% of the cells that were starved for 2 hr maintained PHO4-dependent expression for over eleven generations of growing in high phosphate. This commitment to activation of the Pho regulon depends on two feedback loops that reduce internal phosphate, one through induction of the PHM1-4 genes that increase phosphate storage in the vacuoles and the second by induction of SPL2, which reduces incoming flux by inhibiting low-affinity transporters. Noise in SPL2expression allows stochastic repression of the Pho regulon in committed cells growing at high phosphate, as we demonstrate using a novel method, DAmP multiple copy array (DaMCA), that reduces intrinsic noise in gene expression while maintaining mean abundance. Commitment is an integral part of the dual-transporter motif that helps cells prepare for nutrient depletion.
引用
收藏
页码:2051 / 2057
页数:7
相关论文
共 47 条
  • [41] Gene expression analysis using strains constructed by NHEJ-mediated one-step promoter cloning in the yeast Kluyveromyces marxianus
    Suzuki, Ayako
    Fujii, Hiroshi
    Hoshida, Hisashi
    Akada, Rinji
    FEMS YEAST RESEARCH, 2015, 15 (06)
  • [42] Fine-tuning the expression of pathway gene in yeast using a regulatory library formed by fusing a synthetic minimal promoter with different Kozak variants
    Xu, Liping
    Liu, Pingping
    Dai, Zhubo
    Fan, Feiyu
    Zhang, Xueli
    MICROBIAL CELL FACTORIES, 2021, 20 (01)
  • [43] Poly(A) site choice and Pol2 CTD Serine-5 status govern lncRNA control of phosphate-responsive tgp1 gene expression in fission yeast
    Sanchez, Ana M.
    Shuman, Stewart
    Schwer, Beate
    RNA, 2018, 24 (02) : 237 - 250
  • [44] Assessment of tris (1, 3-dichloro-2-propyl) phosphate toxicology in PC12 cells by using digital gene expression profiling
    Li, Li
    Jiang, Shuai
    Li, Kang
    Lin, Bencheng
    Wang, Ziyu
    Zhang, Zhiqing
    Fang, Yanjun
    CHEMOSPHERE, 2017, 183 : 353 - 360
  • [45] Gene expression profiles of the thermotolerant yeast Saccharomyces cerevisiae strain KKU-VN8 during high-temperature ethanol fermentation using sweet sorghum juice
    Techaparin, Atiya
    Thanonkeo, Pornthap
    Klanrit, Preekamol
    BIOTECHNOLOGY LETTERS, 2017, 39 (10) : 1521 - 1527
  • [46] Production of Candida antarctica Lipase B Gene Open Reading Frame Using Automated PCR Gene Assembly Protocol on Robotic Workcell and Expression in an Ethanologenic Yeast for Use as Resin-Bound Biocatalyst in Biodiesel Production
    Hughes, Stephen R.
    Moser, Bryan R.
    Harmsen, Amanda J.
    Bischoff, Kenneth M.
    Jones, Marjorie A.
    Pinkelman, Rebecca
    Bang, Sookie S.
    Tasaki, Ken
    Doll, Kenneth M.
    Qureshi, Nasib
    Saha, Badal C.
    Liu, Siqing
    Jackson, John S.
    Robinson, Samantha
    Cotta, Michael C.
    Rich, Joseph O.
    Caimi, Paolo
    JALA, 2011, 16 (01): : 17 - 37
  • [47] REEVALUATION OF THE 9 COMPOUNDS REPORTED CONCLUSIVE POSITIVE IN YEAST SACCHAROMYCES-CEREVISIAE ANEUPLOIDY TEST SYSTEMS BY THE GENE-TOX PROGRAM USING STRAIN D61.M OF SACCHAROMYCES-CEREVISIAE
    ALBERTINI, S
    MUTATION RESEARCH, 1991, 260 (02): : 165 - 180