Evidence map›Paper›PMID 32648240›Full record

ArticleBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2020

The H741D mutation in Tac1p contributes to the upregulation of CDR1 and CDR2 expression in Candida albicans.

Jin-Yan Liu, Bing Wei, Ying Wang, Ce Shi, Wen-Jing Li, Yue Zhao, Ling-Ning Meng, Ming-Jie Xiang

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 42% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
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  6. Review
  7. Emergence and circulation of azole-resistantFrontiers in cellular and infection microbiology · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Jin-Yan LiuDepartment of Laboratory Medicine, Ruijin Hospital / Lu Wan Branch, School of Medicine, Shanghai Jiao Tong University School of Medicine, No. 149 South Chongqing Road, Shanghai, China.
Bing WeiDepartment of Laboratory Medicine, The International Peace Maternity & Child Health Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Ying WangDepartment of Clinical Laboratory, Southern District of Anhui Provincial Hospital, Hefei, China.
Ce ShiDepartment of Laboratory Medicine, Ruijin Hospital / Lu Wan Branch, School of Medicine, Shanghai Jiao Tong University School of Medicine, No. 149 South Chongqing Road, Shanghai, China.
Wen-Jing LiDepartment of Laboratory Medicine, Ruijin Hospital / Lu Wan Branch, School of Medicine, Shanghai Jiao Tong University School of Medicine, No. 149 South Chongqing Road, Shanghai, China.
Yue ZhaoDepartment of Laboratory Medicine, Ruijin Hospital / Lu Wan Branch, School of Medicine, Shanghai Jiao Tong University School of Medicine, No. 149 South Chongqing Road, Shanghai, China.
Ling-Ning MengDepartment of Laboratory Medicine, Ruijin Hospital / Lu Wan Branch, School of Medicine, Shanghai Jiao Tong University School of Medicine, No. 149 South Chongqing Road, Shanghai, China.
Ming-Jie XiangDepartment of Laboratory Medicine, Ruijin Hospital / Lu Wan Branch, School of Medicine, Shanghai Jiao Tong University School of Medicine, No. 149 South Chongqing Road, Shanghai, China. mjxiang123456@126.com.ORCID http://orcid.org/0000-0002-8028-0385
Shanghai Jiao Tong University · CNAnhui Provincial Hospital · CN

Funding

Program of Shanghai Key Specialty ZK2012A21Program of Shanghai Municipal Commission of Health and Family Planning 201740069Program of Shanghai Municipal Commission of Health and Family Planning 201840227Program of Shanghai Municipal Huangpu District Commission of Health and Family Planning HKM201702Program of Shanghai Natural Science Foundation 15ZR1426900the Program of National Natural Science Fund Project 81871706
6 · The paper itself

Abstract

The wide use of antifungal agents has led to the development of resistance in the pathogenic yeast strain Candida albicans. Gain-of-function mutations in transcription factors such as Tac1p demonstrated their ability to control expression of the ABC transporter genes CDR1 and CDR2, and mediation of azole resistance. Previously, we obtained a series of azole-resistant isolates with high-level expression of CDR1 or/and CDR2, and identified the novel H741D mutation in Tac1p. In the present study, the TAC1 alleles from isolate C13 were introduced into tac1Δ/Δ mutant. The H741D change was seen in TAC1

Indexed as

Candida albicansDrug Resistance, FungalFluconazoleFungal ProteinsGene Expression Regulation, FungalItraconazoleMembrane Transport ProteinsMutationTranscription FactorsCDR1 protein, Candida albicansFluconazoleFungal ProteinsItraconazoleMembrane Transport ProteinsTranscription FactorsABC transporterAzole resistanceCandida albicansGain-of-function mutationTAC1

Identifiers

PMID32648240
PMCPMC7688751
OpenAlexW3040792590

What OpenQuestion holds

Textmetadata
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.