Evidence map›Paper›PMID 20032305›Full record

ArticleMolecular biology of the cell2010

Regulation of tRNA bidirectional nuclear-cytoplasmic trafficking in Saccharomyces cerevisiae.

Athulaprabha Murthi, Hussam H Shaheen, Hsiao-Yun Huang, Melanie A Preston, Tsung-Po Lai, Eric M Phizicky, Anita K Hopper

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 92 citations in OpenAlex.

  1. Review
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  4. Review
  5. Article
  6. Gle1 is required for tRNA to stimulate Dbp5 ATPase activitybioRxiv : the preprint server for biology · 2023
    Article
  7. The life and times of a tRNA.RNA (New York, N.Y.) · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Article
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  19. Review
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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Athulaprabha MurthiDepartment of Molecular Genetics, Graduate Program in Molecular, Cellular, and Developmental Biology, Center for RNA Biology, The Ohio State University, Columbus, OH 43210, USA
Hussam H Shaheen
Hsiao-Yun Huang
Melanie A Preston
Tsung-Po Lai
Eric M Phizicky
Anita K Hopper
Laboratory of Molecular Genetics · PLThe Ohio State University · USUniversity of Rochester · USInstitut thématique Génétique, génomique et bioinformatique · FR

Funding

TRNA SPLICINGR01GM052347 · NIGMS · UNIVERSITY OF ROCHESTER · PI Eric M. Phizicky · 1995 to 2026
$9.6M
YEAST GENES IN RNA PROCESSING &NUCLEUS/CYTOSOL EXCHANGER01GM027930 · NIGMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI HOPPER, ANITA K · 1985 to 2014
$4.6M
Training in Cellular, Biochemical and Molecular SciencesT32GM068411 · NIGMS · UNIVERSITY OF ROCHESTER · PI MAQUAT, LYNNE E · 2005 to 2019
$3.9M
NIGMS NIH HHS GM068411NIGMS NIH HHS GM27930NIGMS NIH HHS GM52347NIGMS NIH HHS R01 GM027930NIGMS NIH HHS R01 GM052347NIGMS NIH HHS T32 GM068411
6 · The paper itself

Abstract

tRNAs in yeast and vertebrate cells move bidirectionally and reversibly between the nucleus and the cytoplasm. We investigated roles of members of the beta-importin family in tRNA subcellular dynamics. Retrograde import of tRNA into the nucleus is dependent, directly or indirectly, upon Mtr10. tRNA nuclear export utilizes at least two members of the beta-importin family. The beta-importins involved in nuclear export have shared and exclusive functions. Los1 functions in both the tRNA primary export and the tRNA reexport processes. Msn5 is unable to export tRNAs in the primary round of export if the tRNAs are encoded by intron-containing genes, and for these tRNAs Msn5 functions primarily in their reexport to the cytoplasm. The data support a model in which tRNA retrograde import to the nucleus is a constitutive process; in contrast, reexport of the imported tRNAs back to the cytoplasm is regulated by the availability of nutrients to cells and by tRNA aminoacylation in the nucleus. Finally, we implicate Tef1, the yeast orthologue of translation elongation factor eEF1A, in the tRNA reexport process and show that its subcellular distribution between the nucleus and cytoplasm is dependent upon Mtr10 and Msn5.

Indexed as

Active Transport, Cell NucleusAnimalsbeta KaryopherinsIn Situ Hybridization, FluorescenceKaryopherinsNuclear Pore Complex ProteinsNucleocytoplasmic Transport ProteinsPeptide Elongation Factor 1RNA-Binding ProteinsRNA, TransferSaccharomyces cerevisiaeSaccharomyces cerevisiae Proteinsbeta KaryopherinsKaryopherinsLos1 protein, S cerevisiaeMSN5 protein, S cerevisiaeMTR10 protein, S cerevisiaeNuclear Pore Complex ProteinsNucleocytoplasmic Transport ProteinsPeptide Elongation Factor 1RNA-Binding ProteinsRNA, TransferSaccharomyces cerevisiae ProteinsTEF1 protein, S cerevisiae

Identifiers

PMID20032305
PMCPMC2820427
OpenAlexW2146494447

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.