Keyword search (4,163 papers available)

"Omran RP" Authored Publications:

Title Authors PubMed ID
1 Tri-Functional CRISPR Screen Reveals Overexpression of em QDR2 /em and em QDR3 /em Transporters Increase Fumaric Acid Production in em Kluyveromyces marxianus /em Thornbury M; Omran RP; Kumar L; Knoops A; Abushahin R; Whiteway M; Martin VJJ; 41277095
BIOLOGY
2 Candida albicans exhibits heterogeneous and adaptive cytoprotective responses to anti-fungal compounds Dumeaux V; Massahi S; Bettauer V; Mottola A; Dukovny A; Khurdia SS; Costa ACBP; Omran RP; Simpson S; Xie JL; Whiteway M; Berman J; Hallett MT; 37888959
BIOLOGY
3 A Deep Learning Approach to Capture the Essence of Candida albicans Morphologies Bettauer V; Costa ACBP; Omran RP; Massahi S; Kirbizakis E; Simpson S; Dumeaux V; Law C; Whiteway M; Hallett MT; 35972285
BIOLOGY
4 Transcriptional Profiling of the Candida albicans Response to the DNA Damage Agent Methyl Methanesulfonate Feng Y; Zhang Y; Li J; Omran RP; Whiteway M; Feng J; 35886903
BIOLOGY
5 SAGA Complex Subunits in Candida albicans Differentially Regulate Filamentation, Invasiveness, and Biofilm Formation Rashid S; Correia-Mesquita TO; Godoy P; Omran RP; Whiteway M; 35350439
BIOLOGY
6 The zinc cluster transcription factor Rha1 is a positive filamentation regulator in Candida albicans Omran RP; Ramírez-Zavala B; Aji Tebung W; Yao S; Feng J; Law C; Dumeaux V; Morschhäuser J; Whiteway M; 34849863
PERFORM
7 Signal-mediated localization of Candida albicans pheromone response pathway components Costa ACBP; Omran RP; Law C; Dumeaux V; Whiteway M; 33793759
PERFORM
8 Hof1 plays a checkpoint related role in MMS induced DNA damage response in Candida albicans. Feng J, Islam A, Bean B, Feng J, Sparapani S, Shrivastava M, Goyal A, Omran RP, Mallick J, Whiteway M 31940254
BIOLOGY
9 RNA sequencing reveals an additional Crz1-binding motif in promoters of its target genes in the human fungal pathogen Candida albicans. Xu H, Fang T, Omran RP, Whiteway M, Jiang L 31900175
BIOLOGY
10 Screening of Candida albicans GRACE library revealed a unique pattern of biofilm formation under repression of the essential gene ILS1. Costa ACBP, Omran RP, Correia-Mesquita TO, Dumeaux V, Whiteway M 31235750
PERFORM
11 MAP Kinase Regulation of the Candida albicans Pheromone Pathway. Rastghalam G, Omran RP, Alizadeh M, Fulton D, Mallick J, Whiteway M 30787119
BIOLOGY
12 Mms21: A Putative SUMO E3 Ligase in Candida albicans That Negatively Regulates Invasiveness and Filamentation, and Is Required for the Genotoxic and Cellular Stress Response. Islam A, Tebbji F, Mallick J, Regan H, Dumeaux V, Omran RP, Whiteway M 30530734
PERFORM
13 Put3 Positively Regulates Proline Utilization in Candida albicans. Tebung WA, Omran RP, Fulton DL, Morschhäuser J, Whiteway M 29242833
BIOLOGY

 

Title:Put3 Positively Regulates Proline Utilization in Candida albicans.
Authors:Tebung WAOmran RPFulton DLMorschhäuser JWhiteway M
Link:https://www.ncbi.nlm.nih.gov/pubmed/29242833?dopt=Abstract
Publication:
Keywords:
PMID:29242833 Category:mSphere Date Added:2019-05-31
Dept Affiliation: BIOLOGY
1 Chemistry and Biochemistry Department, Concordia University, Montreal, Quebec, Canada.
2 Biology Department, Concordia University, Montreal, Quebec, Canada.
3 Institut für Molekulare Infektionsbiologie, Universität Würzburg, Würzburg, Germany.

Description:

Put3 Positively Regulates Proline Utilization in Candida albicans.

mSphere. 2017 Nov-Dec;2(6):

Authors: Tebung WA, Omran RP, Fulton DL, Morschhäuser J, Whiteway M

Abstract

The zinc cluster transcription factor Put3 was initially characterized in Saccharomyces cerevisiae as the transcriptional activator of PUT1 and PUT2, two genes acting early in the proline assimilation pathway. We have used phenotypic studies, transcription profiling, and chromatin immunoprecipitation with microarray technology (ChIP-chip) to establish that unlike S. cerevisiae, which only uses proline as a nitrogen source, Candida albicans can use proline as a nitrogen source, a carbon source, or a source of both nitrogen and carbon. However, a C. albicans put3 null mutant cannot grow on proline, suggesting that as in S. cerevisiae, C. albicans Put3 (CaPut3) is required for proline catabolism, and because the C. albicans put3 null mutant grew efficiently on glutamate as the sole carbon or nitrogen source, it appears that CaPut3 also regulates the early genes of the pathway. CaPut3 showed direct binding to the CaPUT1 promoter, and both PUT1 and PUT2 were upregulated in response to proline addition in a Put3-dependent manner, as well as in a C. albicans strain expressing a hyperactive Put3. CaPut3 directs proline degradation even in the presence of a good nitrogen source such as ammonia, which contrasts with S. cerevisiae Put3 (ScPut3)-regulated proline catabolism, which only occurs in the absence of a rich nitrogen source. Thus, while overall proline regulatory circuitry differs between S. cerevisiae and C. albicans, the specific role of Put3 appears fundamentally conserved. IMPORTANCECandida albicans poses a significant threat to the lives of immunocompromised people. Historically, knowledge has been drawn from studies on Saccharomyces cerevisiae to understand the pathogen, and many Candida albicans genes are named after their S. cerevisiae orthologs. Direct studies on the pathogen have, however, revealed differences in the roles of some orthologous proteins in the two yeasts. We show that the Put3 transcription factor allows the pathogen to completely degrade proline to usable nitrogen and carbon by evading regulatory restrictions imposed on its S. cerevisiae ortholog, which mandates conditional use of proline only as a nitrogen source in the baker's yeast. The ability of Candida albicans to freely obtain nutrients from multiple sources may help it thrive as a commensal and opportunistic pathogen.

PMID: 29242833 [PubMed]





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