Evidence map›Paper›PMID 25606464›Full record

ArticleMeta gene2014

let-65 is cytoplasmic methionyl tRNA synthetase in C. elegans.

Maha Z Alriyami, Martin R Jones, Robert C Johnsen, Yajnavalka Banerjee, David L Baillie

Open access · hybridAbstract read
In one paragraph

Article in Meta gene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 90% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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

5 authors at 3 institutions in 2 countries.

Maha Z AlriyamiDepartment of Molecular Biology and Biochemistry, Simon Fraser University Burnaby, 8888 University Drive, Burnaby, BC V5A 1S6 Canada ; Department of Biochemistry, College of Medicine and Health Sciences, Sultan Qaboos University, 35, Al-Khod 123, Oman.
Martin R JonesGenome Sciences Centre, British Columbia Cancer Research Centre, 600 West 10th Avenue, Vancouver, BC V5Z 4E6, Canada.
Robert C JohnsenDepartment of Molecular Biology and Biochemistry, Simon Fraser University Burnaby, 8888 University Drive, Burnaby, BC V5A 1S6 Canada.
Yajnavalka BanerjeeDepartment of Biochemistry, College of Medicine and Health Sciences, Sultan Qaboos University, 35, Al-Khod 123, Oman.
David L BaillieDepartment of Molecular Biology and Biochemistry, Simon Fraser University Burnaby, 8888 University Drive, Burnaby, BC V5A 1S6 Canada.
Simon Fraser University · CAGenome British Columbia · CASultan Qaboos University · OM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytoplasmic methionyl tRNA synthetase (MetRS) is one of more than 20 cytoplasmic aminoacyl tRNA synthetase enzymes (ARS). This family of enzymes catalyzes a process fundamental for protein translation. Using a combination of genetic mapping, oligonucleotide array comparative genomic hybridization, and phenotypic correlation, we show that mutations in the essential gene, let-65, reside within the predicted Caenorhabditis elegans homologue of MetRS, which we have named mars-1. We demonstrate that the lethality associated with alleles of let-65 is fully rescued by a transgenic array that spans the mars-1 genomic region. Furthermore, sequence analysis reveals that six let-65 alleles lead to the alteration of highly conserved amino acids.

Indexed as

Aminoacyl tRNA synthetase, methionyl-tRNA synthetaseCaenorhabditis elegansEssential geneslet-65Oligonucleotide array comparative genomic hybridization

Identifiers

PMID25606464
PMCPMC4287814
OpenAlexW2068309135

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.