Rapid and reversible nuclear accumulation of cytoplasmic tRNA in response to nutrient availability

被引:84
作者
Whitney, Michael L.
Hurto, Rebecca L.
Shaheen, Hussam H.
Hopper, Anita K. [1 ]
机构
[1] Penn State Univ, Coll Med, Dept Biochem & Mol Biol, Hershey, PA 17033 USA
[2] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
关键词
D O I
10.1091/mbc.E07-01-0006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytoplasmic tRNAs have recently been found to accumulate in the nucleus during amino acid starvation in yeast. The mechanism and regulation by which tRNAs return to the nucleus are unclear. Here, we show accumulation of cytoplasmic tRNA in the nucleus also occurs during glucose starvation. Nuclear accumulation of tRNA in response to acute glucose or amino acid starvation is rapid, reversible, requires no new transcription, and is independent of the aminoacylation status of tRNA. Gradual depletion of nutrients also results in the accrual of tRNA in the nucleus. Distinct signal transduction pathways seem to be involved in the accumulation of cytoplasmic tRNA in the nucleus in response to amino acid versus glucose starvation. These findings suggest tRNA nucleocytoplasmic distribution may play a role in gene expression in response to nutritional stress.
引用
收藏
页码:2678 / 2686
页数:9
相关论文
共 40 条
[1]   Rapid tRNA decay can result from lack of nonessential modifications [J].
Alexandrov, A ;
Chernyakov, I ;
Gu, WF ;
Hiley, SL ;
Hughes, TR ;
Grayhack, EJ ;
Phizicky, EM .
MOLECULAR CELL, 2006, 21 (01) :87-96
[2]  
[Anonymous], 1991, Methods Enzymol, V194, P1
[3]   Glucose depletion rapidly inhibits translation initiation in yeast [J].
Ashe, MP ;
De Long, SK ;
Sachs, AB .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (03) :833-848
[4]   Role of nuclear pools of Aminoacyl-tRNA synthetases in tRNA nuclear export [J].
Azad, AK ;
Stanford, DR ;
Sarkar, S ;
Hopper, AK .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (05) :1381-1392
[5]  
Barbe Esther, 1996, MEDITERR POLIT, V1, P25
[6]   Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies [J].
Brengues, M ;
Teixeira, D ;
Parker, R .
SCIENCE, 2005, 310 (5747) :486-489
[7]   CAMP-INDEPENDENT CONTROL OF SPORULATION, GLYCOGEN-METABOLISM, AND HEAT-SHOCK RESISTANCE IN S-CEREVISIAE [J].
CAMERON, S ;
LEVIN, L ;
ZOLLER, M ;
WIGLER, M .
CELL, 1988, 53 (04) :555-566
[8]   Elucidating TOR signaling and rapamycin action:: lessons from Saccharomyces cerevisiae [J].
Crespo, JL ;
Hall, MN .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2002, 66 (04) :579-+
[9]   PHOSPHORYLATION OF INITIATION FACTOR-2-ALPHA BY PROTEIN-KINASE GCN2 MEDIATES GENE-SPECIFIC TRANSLATIONAL CONTROL OF GCN4 IN YEAST [J].
DEVER, TE ;
FENG, L ;
WEK, RC ;
CIGAN, AM ;
DONAHUE, TF ;
HINNEBUSCH, AG .
CELL, 1992, 68 (03) :585-596
[10]   Uncharged tRNA activates GCN2 by displacing the protein kinase moiety from a bipartite tRNA-Binding domain [J].
Dong, JS ;
Qiu, HF ;
Garcia-Barrio, M ;
Anderson, J ;
Hinnebusch, AG .
MOLECULAR CELL, 2000, 6 (02) :269-279