Structure theorems and the dynamics of nitrogen catabolite repression in yeast

被引:19
作者
Boczko, EM [1 ]
Cooper, TG
Gedeon, T
Mischaikow, K
Murdock, DG
Pratap, S
Wells, KS
机构
[1] Vanderbilt Univ, Dept Biomed Informat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Div Med Genet, Nashville, TN 37232 USA
[4] Univ Tennessee, Dept Mol Sci, Memphis, TN 38163 USA
[5] Montana State Univ, Dept Math Sci, Bozeman, MT 59717 USA
[6] Georgia Inst Technol, Dept Math, Atlanta, GA 30332 USA
关键词
delay equations; GATA factors; GLN3;
D O I
10.1073/pnas.0501339102
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
07 ; 0710 ; 09 ;
摘要
By using current biological understanding, a conceptually simple, but mathematically complex, model is proposed for the dynamics of the gene circuit responsible for regulating nitrogen catabolite repression (NCR) in yeast. A variety of mathematical "structure" theorems are described that allow one to determine the asymptotic dynamics of complicated systems under very weak hypotheses. It is shown that these theorems apply to several subcircuits of the full NCR circuit, most importantly to the URE2-GLN3 subcircuit that is independent of the other constituents but governs the switching behavior of the full NCR circuit under changes in nitrogen source. Under hypotheses that are fully consistent with biological data, it is proven that the dynamics of this subcircuit is simple periodic behavior in synchrony with the cell cycle. Although the current mathematical structure theorems do not apply to the full NCR circuit, extensive simulations suggest that the dynamics is constrained in much the same way as that of the URE2-GLN3 subcircuit. This finding leads to the proposal that mathematicians study genetic circuits to find new geometries for which structure theorems may exist.
引用
收藏
页码:5647 / 5652
页数:6
相关论文
共 40 条
  • [1] Development and characterization of a reconstituted yeast translation initiation system
    Algire, MA
    Maag, D
    Savio, P
    Acker, MG
    Tarun, SZ
    Sachs, AB
    Asano, K
    Nielsen, KH
    Olsen, DS
    Phan, L
    Hinnebusch, AG
    Lorsch, JR
    [J]. RNA, 2002, 8 (03) : 382 - 397
  • [2] The TOR signalling pathway controls nuclear localization of nutrient-regulated transcription factors
    Beck, T
    Hall, MN
    [J]. NATURE, 1999, 402 (6762) : 689 - 692
  • [3] Benaim M., 1996, Journal of Dynamics and Differential Equations, V8, P141, DOI 10.1007/BF02218617
  • [4] Tripartite regulation of Gln3p by TOR, Ure2p, and phosphatases
    Bertram, PG
    Choi, JH
    Carvalho, J
    Ai, WD
    Zeng, CB
    Chan, TF
    Zheng, XFS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (46) : 35727 - 35733
  • [5] Noise in eukaryotic gene expression
    Blake, WJ
    Kærn, M
    Cantor, CR
    Collins, JJ
    [J]. NATURE, 2003, 422 (6932) : 633 - 637
  • [6] THE EFFECTS OF DIMENSION AND SIZE FOR A COMPARTMENTAL MODEL OF REPRESSION
    BUSENBERG, SN
    MAHAFFY, JM
    [J]. SIAM JOURNAL ON APPLIED MATHEMATICS, 1988, 48 (04) : 882 - 903
  • [7] Phosphorylation regulates the interaction between Gln3p and the nuclear import factor Srp1p
    Carvalho, J
    Bertram, PG
    Wente, SR
    Zheng, XFS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (27) : 25359 - 25365
  • [8] WHAT IS THE BACTERIAL-GROWTH LAW DURING THE DIVISION CYCLE
    COOPER, S
    [J]. JOURNAL OF BACTERIOLOGY, 1988, 170 (11) : 5001 - 5005
  • [9] Transmitting the signal of excess nitrogen in Saccharomyces cerevisiae from the Tor proteins to the GATA factors:: connecting the dots
    Cooper, TG
    [J]. FEMS MICROBIOLOGY REVIEWS, 2002, 26 (03) : 223 - 238
  • [10] Cytoplasmic Compartmentation of Gln3 during nitrogen catabolite repression and the mechanism of its nuclear localization during carbon starvation in Saccharomyces cerevisiae
    Cox, KH
    Tate, JJ
    Cooper, TG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (40) : 37559 - 37566