Evidence map›Paper›PMID 33828169›Full record

ArticleScientific reports2021

Efficient collection of a large number of mutations by mutagenesis of DNA damage response defective animals.

Yuji Suehiro, Sawako Yoshina, Tomoko Motohashi, Satoru Iwata, Katsufumi Dejima, Shohei Mitani

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Yuji Suehiro *Department of Physiology, Tokyo Women's Medical University, Shinjuku, Tokyo, Japan.
Sawako Yoshina *Department of Physiology, Tokyo Women's Medical University, Shinjuku, Tokyo, Japan.
Tomoko MotohashiDepartment of Physiology, Tokyo Women's Medical University, Shinjuku, Tokyo, Japan.
Satoru IwataChubu University Center for Education in Laboratory Animal Research, Kasugai, Aichi, Japan.
Katsufumi DejimaDepartment of Physiology, Tokyo Women's Medical University, Shinjuku, Tokyo, Japan.
Shohei MitaniDepartment of Physiology, Tokyo Women's Medical University, Shinjuku, Tokyo, Japan. mitani.shohei@twmu.ac.jp.
Tokyo Women's Medical University · JPChubu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the development of massive parallel sequencing technology, it has become easier to establish new model organisms that are ideally suited to the specific biological phenomena of interest. Considering the history of research using classical model organisms, we believe that the efficient construction and sharing of gene mutation libraries will facilitate the progress of studies using these new model organisms. Using C. elegans, we applied the TMP/UV mutagenesis method to animals lacking function in the DNA damage response genes atm-1 and xpc-1. This method produces genetic mutations three times more efficiently than mutagenesis of wild-type animals. Furthermore, we confirmed that the use of next-generation sequencing and the elimination of false positives through machine learning could automate the process of mutation identification with an accuracy of over 95%. Eventually, we sequenced the whole genomes of 488 strains and isolated 981 novel mutations generated by the present method; these strains have been made available to anyone who wants to use them. Since the targeted DNA damage response genes are well conserved and the mutagens used in this study are also effective in a variety of species, we believe that our method is generally applicable to a wide range of animal species.

Indexed as

AnimalsAtaxia Telangiectasia Mutated ProteinsBase SequenceCaenorhabditis elegansCaenorhabditis elegans ProteinsDNADNA DamageDNA RepairGene LibraryGenetic TechniquesHigh-Throughput Nucleotide SequencingMutagenesisMutagenesis, Site-DirectedMutagensMutationPhenotypeAtaxia Telangiectasia Mutated Proteinsatm-1 protein, C elegansCaenorhabditis elegans ProteinsDNAMutagens

Identifiers

PMID33828169
PMCPMC8027614
OpenAlexW3148820183

What OpenQuestion holds

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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.