PMID- 14640976 OWN - NLM STAT- MEDLINE DCOM- 20040624 LR - 20181113 IS - 1470-8728 (Electronic) IS - 0264-6021 (Print) IS - 0264-6021 (Linking) VI - 378 IP - Pt 3 DP - 2004 Mar 15 TI - The nuclear tRNA aminoacylation-dependent pathway may be the principal route used to export tRNA from the nucleus in Saccharomyces cerevisiae. PG - 809-16 AB - Nuclear tRNA export in Saccharomyces cerevisiae has been proposed to involve three pathways, designated Los1p-dependent, Los1p-independent nuclear aminoacylation-dependent, and Los1p- and nuclear aminoacylation-independent. Here, a comprehensive biochemical analysis was performed to identify tRNAs exported by the aminoacylation-dependent and -independent pathways of S. cerevisiae. Interestingly, the major tRNA species of at least 19 families were found in the aminoacylated form in the nucleus. tRNAs known to be exported by the export receptor Los1p were also aminoacylated in the nucleus of both wild-type and mutant Los1p strains. FISH (fluorescence in situ hybridization) analyses showed that tRNA(Tyr) co-localizes with the U18 small nucleolar RNA in the nucleolus of a tyrosyl-tRNA synthetase mutant strain defective in nuclear tRNA(Tyr) export because of a block in nuclear tRNA(Tyr) aminoacylation. tRNA(Tyr) was also found in the nucleolus of a utp8 mutant strain defective in nuclear tRNA export but not nuclear tRNA aminoacylation. These results strongly suggest that the nuclear aminoacylation-dependent pathway is principally responsible for tRNA export in S. cerevisiae and that Los1p is an export receptor of this pathway. It is also likely that in mammalian cells tRNAs are mainly exported from the nucleus by the nuclear aminoacylation-dependent pathway. In addition, the data are consistent with the idea that nuclear aminoacylation is used as a quality control mechanism for ensuring nuclear export of only mature and functional tRNAs, and that this quality assurance step occurs in the nucleolus. FAU - Steiner-Mosonyi, Marta AU - Steiner-Mosonyi M AD - Guelph-Waterloo Center for Graduate Work in Chemistry and Biochemistry, Department of Chemistry and Biochemistry, University of Guelph, Guelph, Ontario N1G 2W1, Canada. FAU - Mangroo, Dev AU - Mangroo D LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Biochem J JT - The Biochemical journal JID - 2984726R RN - 0 (Los1 protein, S cerevisiae) RN - 0 (Nuclear Pore Complex Proteins) RN - 0 (RNA, Transfer, Amino Acyl) RN - 0 (RNA, Transfer, Tyr) RN - 0 (Saccharomyces cerevisiae Proteins) RN - 9014-25-9 (RNA, Transfer) SB - IM MH - Active Transport, Cell Nucleus MH - Cell Nucleolus/chemistry MH - Cell Nucleus/chemistry/*metabolism MH - Mutation MH - Nuclear Pore Complex Proteins/metabolism MH - RNA, Transfer/*metabolism MH - RNA, Transfer, Amino Acyl/analysis/*metabolism MH - RNA, Transfer, Tyr/analysis MH - Saccharomyces cerevisiae/chemistry/genetics/*metabolism MH - Saccharomyces cerevisiae Proteins/metabolism MH - Signal Transduction PMC - PMC1224000 EDAT- 2003/12/03 05:00 MHDA- 2004/06/25 05:00 PMCR- 2004/09/15 CRDT- 2003/12/03 05:00 PHST- 2003/11/28 00:00 [accepted] PHST- 2003/11/05 00:00 [revised] PHST- 2003/08/26 00:00 [received] PHST- 2003/12/03 05:00 [pubmed] PHST- 2004/06/25 05:00 [medline] PHST- 2003/12/03 05:00 [entrez] PHST- 2004/09/15 00:00 [pmc-release] AID - BJ20031306 [pii] AID - 10.1042/BJ20031306 [doi] PST - ppublish SO - Biochem J. 2004 Mar 15;378(Pt 3):809-16. doi: 10.1042/BJ20031306.