Fission yeast Tor2 promotes cell growth and represses cell differentiation

被引:125
作者
Alvarez, Beatriz [1 ]
Moreno, Sergio [1 ]
机构
[1] Univ Salamanca, CSIC, Inst Biol Mol & Celular Canc, Salamanca 37007, Spain
关键词
Tor; cell growth; cell differentiation; fission yeast;
D O I
10.1242/jcs.03241
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The fission yeast Schizosaccharomyces pombe is an excellent model system in which to study the coordination of cell growth and cell differentiation. In the presence of nutrients, fission yeast cells grow and divide; in the absence of nutrients, they stop growing and undergo cell differentiation. The molecular mechanisms underlying this response are not fully understood. Here, we demonstrate that Tor2, a fission yeast member of the TOR protein kinase family, is central to controlling the switch between cell growth and cell differentiation in response to nutrient availability. Tor2 controls cell growth and ribosome biogenesis by regulating ribosomal protein gene expression. We have found that Tor2 has an additional function in repressing sexual differentiation. Tor2 overexpression strongly represses mating, meiosis and sporulation efficiency, whereas Tor2 inactivation has the opposite effect, leading to cell differentiation, regardless of the nutritional conditions. This newly revealed function of Tor2 appears to operate by interfering with the functions of the transcription factor Ste11 and the meiosis-promoting RNA-binding protein Mei2. Thus, our data reveal a unique regulatory function of the Tor pathway - ensuring that growth and cell differentiation become mutually exclusive and that the choice between them depends on environmental conditions.
引用
收藏
页码:4475 / 4485
页数:11
相关论文
共 74 条
[21]   Protein kinase A regulates sexual development and gluconeogenesis through phosphorylation of the Zn finger transcriptional activator Rst2p in fission yeast [J].
Higuchi, T ;
Watanabe, Y ;
Yamamoto, M .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (01) :1-11
[22]   Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive [J].
Jacinto, E ;
Loewith, R ;
Schmidt, A ;
Lin, S ;
Rüegg, MA ;
Hall, A ;
Hall, MN .
NATURE CELL BIOLOGY, 2004, 6 (11) :1122-U30
[23]   TOR signalling in bugs, brain and brawn [J].
Jacinto, E ;
Hall, MN .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (02) :117-126
[24]  
Kawai M, 2001, CURR GENET, V39, P166
[25]   A wat1 mutant of fission yeast is defective in cell morphology [J].
Kemp, JT ;
Balasubramanian, MK ;
Gould, KL .
MOLECULAR AND GENERAL GENETICS, 1997, 254 (02) :127-138
[26]   GβL, a positive regulator of the rapamycin-sensitive pathway required for the nutrient-sensitive interaction between raptor and mTOR [J].
Kim, DH ;
Sarbassov, DD ;
Ali, SM ;
Latek, RR ;
Guntur, KVP ;
Erdjument-Bromage, H ;
Tempst, P ;
Sabatini, DM .
MOLECULAR CELL, 2003, 11 (04) :895-904
[27]   MTOR interacts with Raptor to form a nutrient-sensitive complex that signals to the cell growth machinery [J].
Kim, DH ;
Sarbassov, DD ;
Ali, SM ;
King, JE ;
Latek, RR ;
Erdjument-Bromage, H ;
Tempst, P ;
Sabatini, DM .
CELL, 2002, 110 (02) :163-175
[28]   Apc10 and Ste9/Srw1, two regulators of the APC-cyclosome, as well as the CDK inhibitor Rum1 are required for G1 cell-cycle arrest in fission yeast [J].
Kominami, K ;
Seth-Smith, H ;
Toda, T .
EMBO JOURNAL, 1998, 17 (18) :5388-5399
[29]   A zinc-finger protein, Rst2p, regulates transcription of the fission yeast ste11+ gene, which encodes a pivotal transcription factor for sexual development [J].
Kunitomo, H ;
Higuchi, T ;
Iino, Y ;
Yamamoto, M .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (09) :3205-3217
[30]   Two TOR complexes, only one of which is rapamycin sensitive, have distinct roles in cell growth control [J].
Loewith, R ;
Jacinto, E ;
Wullschleger, S ;
Lorberg, A ;
Crespo, JL ;
Bonenfant, D ;
Oppliger, W ;
Jenoe, P ;
Hall, MN .
MOLECULAR CELL, 2002, 10 (03) :457-468