Evidence map›Paper›PMID 30654470›Full record

ArticleViruses2019

A Rapid Method for Sequencing Double-Stranded RNAs Purified from Yeasts and the Identification of a Potent K1 Killer Toxin Isolated from

Angela M Crabtree, Emily A Kizer, Samuel S Hunter, James T Van Leuven, Daniel D New, Matthew W Fagnan, Paul A Rowley

Abstract read
In one paragraph

Article in Viruses, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. ThemBio · 2025
    Article
  6. Article
  7. A Comprehensive Structural and Functional Analysis ofbioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Inhibition of diastatic yeasts byApplied and environmental microbiology · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

7 authors.

Angela M CrabtreeDepartment of Biological Sciences, University of Idaho, Moscow, ID 83844, USA. amcrabtree@uidaho.edu.
Emily A KizerDepartment of Biological Sciences, University of Idaho, Moscow, ID 83844, USA. mrs@jkizer.com.
Samuel S HunterIBEST Genomics Core, University of Idaho, Moscow, ID 83843, USA. shunter@uidaho.edu.
James T Van LeuvenDepartment of Biological Sciences, University of Idaho, Moscow, ID 83844, USA. jvanleuven@uidaho.edu.ORCID 0000-0002-2730-0287
Daniel D NewIBEST Genomics Core, University of Idaho, Moscow, ID 83843, USA. dnew@uidaho.edu.
Matthew W FagnanIBEST Genomics Core, University of Idaho, Moscow, ID 83843, USA. mfagnan@uidaho.edu.
Paul A RowleyDepartment of Biological Sciences, University of Idaho, Moscow, ID 83844, USA. prowley@uidaho.edu.ORCID 0000-0002-3590-5139

Funding

Women's health: interplay of maternal diet and key demographics on neurological health in the rural frontier and remote WestP20GM103408 · NIGMS · UNIVERSITY OF IDAHO · PI Scott A Minnich · 2012 to 2026
$59.8M
Sequence-structure-function relationships in human visual photopigmentsP20GM104420 · NIGMS · UNIVERSITY OF IDAHO · PI WICHMAN, HOLLY A · 2015 to 2024
$22.9M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2014 to 2023
$22.7M
National Science Foundation 0619793National Science Foundation 0923535National Science Foundation 1818368NIGMS NIH HHS P20 GM104420NIGMS NIH HHS P20 GM109095NIH HHS P20 GM103408NIH HHS P20 GM109095
6 · The paper itself

Abstract

Mycoviruses infect a large number of diverse fungal species, but considering their prevalence, relatively few high-quality genome sequences have been determined. Many mycoviruses have linear double-stranded RNA genomes, which makes it technically challenging to ascertain their nucleotide sequence using conventional sequencing methods. Different specialist methodologies have been developed for the extraction of double-stranded RNAs from fungi and the subsequent synthesis of cDNAs for cloning and sequencing. However, these methods are often labor-intensive, time-consuming, and can require several days to produce cDNAs from double-stranded RNAs. Here, we describe a comprehensive method for the rapid extraction and sequencing of dsRNAs derived from yeasts, using short-read next generation sequencing. This method optimizes the extraction of high-quality double-stranded RNAs from yeasts and 3' polyadenylation for the initiation of cDNA synthesis for next-generation sequencing. We have used this method to determine the sequence of two mycoviruses and a double-stranded RNA satellite present within a single strain of the model yeast

Indexed as

Cloning, MolecularDNA, ComplementaryHigh-Throughput Nucleotide SequencingKiller Factors, YeastMutationRNA, Double-StrandedRNA, ViralSaccharomyces cerevisiaeDNA, ComplementaryK1 killer toxinKiller Factors, YeastRNA, Double-StrandedRNA, ViraldsRNAkiller toxinmycovirussequencingtotivirus

Identifiers

PMID30654470
PMCPMC6356530

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.