Evidence map›Paper›PMID 29357302›Full record

ArticleFungal genetics and biology : FG & B2018

Role of the inositol pyrophosphate multikinase Kcs1 in Cryptococcus inositol metabolism.

Guojian Liao, Yina Wang, Tong-Bao Liu, Gurkirat Kohli, Weidong Qian, Erika Shor, Selvakumar Subbian, Chaoyang Xue

Abstract read
In one paragraph

Article in Fungal genetics and biology : FG & B, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 27% 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, 10 citations in OpenAlex.

  1. Review
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  3. Arg1 frommBio · 2024
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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

8 authors at 3 institutions in 2 countries.

Guojian LiaoPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA; College of Pharmaceutical Sciences, Southwest University, Chongqing, China.
Yina WangPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Tong-Bao LiuPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Gurkirat KohliPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Weidong QianPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA; Department of Pharmacy, Shaanxi University of Science and Technology, Xian, China.
Erika ShorPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Selvakumar SubbianPublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA.
Chaoyang XuePublic Health Research Institute Center, Rutgers University - New Jersey Medical School, Newark, NJ, USA; Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers University - New Jersey Medical School, Newark, NJ, USA. Electronic address: xuech@njms.rutgers.edu.
Rutgers New Jersey Medical SchoolRutgers, The State University of New Jersey · USShaanxi University of Science and Technology · CN

Funding

The role of inositol in Cryptococcus biology and pathogenesisR01AI123315 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Chaoyang Xue · 2017 to 2026
$5.0M
Regulation of ubiquitin-proteasome in Cryptococcus pathogenesisR21AI115204 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI XUE, CHAOYANG · 2015 to 2016
$437k
NIAID NIH HHS R01 AI123315NIAID NIH HHS R21 AI115204
6 · The paper itself

Abstract

Cryptococcus neoformans is the most common cause of deadly fungal meningitis. This fungus has a complex inositol acquisition and utilization system, and our previous studies have shown the importance of inositol utilization in cryptococcal development and virulence. However, how inositol utilization is regulated in this fungus remains unknown. In this study, we found that inositol, irrespective of the presence of glucose in the media, represses the expression of C. neoformans genes involved in inositol pyrophosphate biosynthesis, including the gene encoding inositol hexakisphosphate kinase Kcs1. Kcs1 was recently reported to regulate inositol metabolism in Saccharomyces cerevisiae and to impact virulence in C. neoformans. To examine the potential role of Kcs1 in inositol regulation in C. neoformans, we generated the kcs1Δ mutant and compared its phenotype with the wild type strain. We found that Kcs1 negatively regulates inositol uptake and catabolism in C. neoformans, but, in contrast to Kcs1 function in S. cerevisiae, does not appear to regulate inositol biosynthesis. Together, these results show that Kcs1 functions to fine-tune inositol acquisition to maintain inositol homeostasis in C. neoformans.

Indexed as

Gene Expression Regulation, FungalCryptococcus neoformansDiphosphatesFungal ProteinsGene DeletionGlucoseHomeostasisInositolPhosphotransferases (Phosphate Group Acceptor)VirulenceDiphosphatesFungal ProteinsGlucoseInositolinositol hexakisphosphate kinasePhosphotransferases (Phosphate Group Acceptor)

Identifiers

PMID29357302
PMCPMC5860976
OpenAlexW2790598219

What OpenQuestion holds

Textmetadata
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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.