Evidence map›Paper›PMID 27449518›Full record

ArticleG3 (Bethesda, Md.)2016

rDNA Copy Number Variants Are Frequent Passenger Mutations in Saccharomyces cerevisiae Deletion Collections and de Novo Transformants.

Elizabeth X Kwan, Xiaobin S Wang, Haley M Amemiya, Bonita J Brewer, M K Raghuraman

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
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  10. Recent insights into the evolution of mutation rates in yeast.Current opinion in genetics & development · 2022
    Review
  11. The long and short of rDNA and yeast replicative aging.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. rDNA array length is a major determinant of replicative lifespan in budding yeast.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
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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 2 institutions in 1 country.

Elizabeth X KwanDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195.
Xiaobin S WangDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195 Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York 10032.
Haley M AmemiyaDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195.
Bonita J BrewerDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195.
M K RaghuramanDepartment of Genome Sciences, University of Washington, Seattle, Washington 98195 raghu@u.washington.edu.
University of Washington · USColumbia University · US

Funding

INTERDISCIPLINARY TRAINING IN GENOMIC SCIENCEST32HG000035 · NHGRI · UNIVERSITY OF WASHINGTON · PI Bruce Colston Trapnell · 1995 to 2026
$24.2M
EUKARYOTIC CHROMOSOME STRUCTURE AND REPLICATIONR01GM018926 · NIGMS · UNIVERSITY OF WASHINGTON · PI BREWER, BONITA J · 1985 to 2016
$6.8M
NHGRI NIH HHS T32 HG000035NIGMS NIH HHS R01 GM018926
6 · The paper itself

Abstract

The Saccharomyces cerevisiae ribosomal DNA (rDNA) locus is known to exhibit greater instability relative to the rest of the genome. However, wild-type cells preferentially maintain a stable number of rDNA copies, suggesting underlying genetic control of the size of this locus. We performed a screen of a subset of the Yeast Knock-Out (YKO) single gene deletion collection to identify genetic regulators of this locus and to determine if rDNA copy number correlates with yeast replicative lifespan. While we found no correlation between replicative lifespan and rDNA size, we identified 64 candidate strains with significant rDNA copy number differences. However, in the process of validating candidate rDNA variants, we observed that independent isolates of our de novo gene deletion strains had unsolicited but significant changes in rDNA copy number. Moreover, we were not able to recapitulate rDNA phenotypes from the YKO yeast deletion collection. Instead, we found that the standard lithium acetate transformation protocol is a significant source of rDNA copy number variation, with lithium acetate exposure being the treatment causing variable rDNA copy number events after transformation. As the effects of variable rDNA copy number are being increasingly reported, our finding that rDNA is affected by lithium acetate exposure suggested that rDNA copy number variants may be influential passenger mutations in standard strain construction in S. cerevisiae.

Indexed as

AcetatesDNA Copy Number VariationsDNA ReplicationDNA, RibosomalGene DeletionGene Knockout TechniquesGenome, FungalPhenotypeRibosomesSaccharomyces cerevisiaeAcetatesDNA, Ribosomallithium acetateCNVlithiumrDNASaccharomyces cerevisiaetransformation

Identifiers

PMID27449518
PMCPMC5015940
OpenAlexW2490409064

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.