Evidence map›Paper›PMID 29856841›Full record

ArticlePloS one2018

Genome-wide screen reveals important roles for ESCRT proteins in drug/ion resistance of fission yeast.

Yikun Yang, Qiannan Liu, Guanglie Jiang, Si Chen, Lina Zhou, Norihiro Sakamoto, Takayoshi Kuno, Yue Fang, Fan Yao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 2 countries.

Yikun YangDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.
Qiannan LiuDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.
Guanglie JiangDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.
Si ChenDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.
Lina ZhouDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.
Norihiro SakamotoDivision of Food and Drug Evaluation Science, Department of Social/Community Medicine and Health Science, Kobe University Graduate School of Medicine, Kobe, Japan.
Takayoshi KunoDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.
Yue FangDepartment of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, China.ORCID 0000-0002-0557-2118
Fan YaoDepartment of Breast Surgery and Surgical Oncology, Research Unit of General Surgery, The First Affiliated Hospital of China Medical University, Shenyang, China.
China Medical University · CNKobe University · JPFirst Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To study sodium homeostasis, we performed a genome-wide screen for deletion strains that show resistance to NaCl. We identified 34 NaCl-resistant strains. Among them, the largest group that consists of 10 genes related to membrane trafficking and 7 out of 10 genes are ESCRT proteins which are involved in cargo transportation into luminal vesicles within the multivesicular body. All of the ESCRT related mutants which showed sodium resistance also showed defects in vacuole fusion. To further understand the role of the ESCRT pathway in various ion homeostasis, we examined sensitivity of these ESCRT mutants to various cation salts other than NaCl, including KCl, LiCl, CaCl2, CoCl2, MgCl2, NiSO4 and MnCl2. While these ESCRT mutants showed resistance to LiCl, CoCl2 and MgCl2, they showed sensitivity to KCl, CaCl2, NiSO4 and MnCl2. Then we examined sensitivity of these ESCRT mutants to various drugs which are known to inhibit the growth of fission yeast cells. While these ESCRT mutants were more or equally sensitive to most of the drugs tested as compared to the wild-type cells, they showed resistance to some drugs such as tamoxifen, fluorouracil and amiodarone. These results suggest that the ESCRT pathway plays important roles in drug/ion resistance of fission yeast.

Indexed as

AmiodaroneCalcineurinDrug Resistance, FungalEndosomal Sorting Complexes Required for TransportGenome, FungalMutationSaccharomyces cerevisiae ProteinsSaltsSalt ToleranceSchizosaccharomycesSodium ChlorideTamoxifenAmiodaroneCalcineurinEndosomal Sorting Complexes Required for TransportSaccharomyces cerevisiae ProteinsSaltsSodium ChlorideTamoxifen

Identifiers

PMID29856841
PMCPMC5983419
OpenAlexW2807513961

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Registered trials

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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.