Evidence map›Paper›PMID 28686685›Full record

ArticlePloS one2017

Comparative proteomic analysis of Gib2 validating its adaptor function in Cryptococcus neoformans.

Gillian O Bruni, Blake Battle, Ben Kelly, Zhengguang Zhang, Ping Wang

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2017. 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
0.7field-weighted citation impact, top 28% 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, 8 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

5 authors at 3 institutions in 2 countries.

Gillian O BruniDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, LA, United States of America.
Blake BattleCollege of Arts and Sciences, Loyola University New Orleans, New Orleans, LA, United States of America.
Ben KellyDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, LA, United States of America.
Zhengguang ZhangDepartment of Plant Pathology, College of Plant Protection, Nanjing Agricultural University, Nanjing, China.
Ping WangDepartment of Microbiology, Immunology, and Parasitology, Louisiana State University Health Sciences Center, New Orleans, LA, United States of America.ORCID http://orcid.org/0000-0002-3851-2779
Louisiana State University Health Sciences Center New Orleans · USLoyola University New Orleans · USNanjing Agricultural University · CN

Funding

Genome editing in Rhizopus delemar using using CRISPR-Cas systemsR21AI121451 · NIAID · LSU HEALTH SCIENCES CENTER · PI WANG, PING · 2016 to 2017
$397k
Genome Engineering of Cryptococcus Neoformans using CRISPR-Cas SystemR03AI121460 · NIAID · LSU HEALTH SCIENCES CENTER · PI WANG, PING · 2016 to 2017
$146k
NIAID NIH HHS R03 AI121460NIAID NIH HHS R21 AI121451
6 · The paper itself

Abstract

Cryptococcus neoformans causes often-fatal fungal meningoencephalitis in immunocompromised individuals. While the exact disease mechanisms remain elusive, signal transduction pathways mediated by key elements such as G-protein α subunit Gpa1, small GTPase Ras1, and atypical Gβ-like/RACK1 protein Gib2 are known to play important roles in C. neoformans virulence. Gib2 is important for normal growth, differentiation, and pathogenicity, and it also positively regulates cAMP levels in conjunction with Gpa1. Interestingly, Gib2 displays a scaffold protein property by interacting with a wide variety of cellular proteins. To explore Gib2 global regulatory functions, we performed two-dimensional differential gel electrophoresis (DIGE) analysis and found that GIB2 disruption results in an increased expression of 304 protein spots (43.4%) and a decreased expression of 396 protein spots (56.6%). Analysis of 96 proteins whose expression changes were deemed significant (≥ +/- 1.5- fold) revealed that 75 proteins belong to at least 12 functional protein groups. Among them, eight groups have the statistical stringency of p ≤ 0.05, and four groups, including Hsp70/71 heat shock protein homologs and ribosomal proteins, survived the Bonferroni correction. This finding is consistent with earlier established roles for the human Gβ-like/RACK1 and the budding yeast Saccharomyces cerevisiae Asc1. It suggests that Gib2 could also be part of the complex affecting ribosomal biogenesis and protein translation in C. neoformans. Since eukaryotic Hsp70/71 proteins are involved in the facilitation of nascent protein folding, processing, and protection of cells against stress, we also propose that Gib2-regulated stress responses are linked to fungal virulence. Collectively, our study supports a conserved role of Gβ-like/RACK/Gib2 proteins in the essential cellular process of ribosomal biogenesis and protein translation. Our study also highlights a multifaceted regulatory role of Gib2 in the growth and pathogenicity of C. neoformans.

Indexed as

Gene Expression Regulation, FungalAdaptor Proteins, Signal TransducingCryptococcus neoformansCyclic AMPElectrophoresis, Gel, Two-DimensionalFungal ProteinsGTP-Binding ProteinsHSP70 Heat-Shock ProteinsMolecular Sequence AnnotationOrganelle BiogenesisProtein BindingProtein BiosynthesisRibosomal ProteinsRibosomesSaccharomyces cerevisiae ProteinsSequence Homology, Amino AcidAdaptor Proteins, Signal TransducingASC1 protein, S cerevisiaeCyclic AMPFungal ProteinsGTP-Binding ProteinsHSP70 Heat-Shock ProteinsRibosomal ProteinsSaccharomyces cerevisiae ProteinsVirulence Factors

Identifiers

PMID28686685
PMCPMC5501510
OpenAlexW2732521051

What OpenQuestion holds

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LicenceCC BY
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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.