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Rewiring of the Ppr1 Zinc Cluster Transcription Factor from Purine Catabolism to Pyrimidine Biogenesis in the Saccharomycetaceae.

Author(s): Tebung WA, Choudhury BI, Tebbji F, Morschhäuser J, Whiteway M

Curr Biol. 2016 07 11;26(13):1677-1687 Authors: Tebung WA, Choudhury BI, Tebbji F, Morschhäuser J, Whiteway M

Article GUID: 27321996
Beauvericin Potentiates Azole Activity via Inhibition of Multidrug Efflux, Blocks Candida albicans Morphogenesis, and Is Effluxed via Yor1 and Circuitry Controlled by Zcf29.

Author(s): Shekhar-Guturja T, Tebung WA, Mount H, Liu N, Köhler JR, Whiteway M, Cowen LE

Antimicrob Agents Chemother. 2016 12;60(12):7468-7480 Authors: Shekhar-Guturja T, Tebung WA, Mount H, Liu N, Köhler JR, Whiteway M, Cowen LE

Article GUID: 27736764
Put3 Positively Regulates Proline Utilization in Candida albicans.

Author(s): Tebung WA, Omran RP, Fulton DL, Morschhäuser J, Whiteway M

mSphere. 2017 Nov-Dec;2(6): Authors: Tebung WA, Omran RP, Fulton DL, Morschhäuser J, Whiteway M

Article GUID: 29242833
Title:Rewiring of the Ppr1 Zinc Cluster Transcription Factor from Purine Catabolism to Pyrimidine Biogenesis in the Saccharomycetaceae.
Authors:Tebung WA,  Choudhury BI,  Tebbji F,  Morschhäuser J,  Whiteway M
Link:https://www.ncbi.nlm.nih.gov/pubmed/27321996?dopt=Abstract
Category:Curr Biol
PMID:27321996
Dept Affiliation: BIOLOGY
1 Chemistry and Biochemistry Department, Concordia University, 7141 Sherbrooke Street West, Montreal, QC H4B 1R6, Canada.
2 Biology Department, Concordia University, 7141 Sherbrooke Street West, Montreal, QC H4B 1R6, Canada.
3 Infectious Diseases Research Centre (CRI), CHU de Québec Research Center (CHUQ), Université Laval, Quebec City, QC G1V 0A6, Canada.
4 Institut für Molekulare Infektionsbiologie, Universität Würzburg, 97070 Würzburg, Germany.
5 Biology Department, Concordia University, 7141 Sherbrooke Street West, Montreal, QC H4B 1R6, Canada. Electronic address: malcolm.whiteway@concordia.ca.

Description:

Rewiring of the Ppr1 Zinc Cluster Transcription Factor from Purine Catabolism to Pyrimidine Biogenesis in the Saccharomycetaceae.

Curr Biol. 2016 07 11;26(13):1677-1687

Authors: Tebung WA, Choudhury BI, Tebbji F, Morschhäuser J, Whiteway M

Abstract

Metabolic pathways are largely conserved in eukaryotes, but the transcriptional regulation of these pathways can sometimes vary between species; this has been termed "rewiring." Recently, it has been established that in the Saccharomyces lineage starting from Naumovozyma castellii, genes involved in allantoin breakdown have been genomically relocated to form the DAL cluster. The formation of the DAL cluster occurred along with the loss of urate permease (UAP) and urate oxidase (UOX), reducing the requirement for oxygen and bypassing the candidate Ppr1 inducer, uric acid. In Saccharomyces cerevisiae, this allantoin catabolism cluster is regulated by the transcription factor Dal82, which is not present in many of the pre-rearrangement fungal species. We have used ChIP-chip analysis, transcriptional profiling of an activated Ppr1 protein, bioinformatics, and nitrogen utilization studies to establish that in Candida albicans the zinc cluster transcription factor Ppr1 controls this allantoin catabolism regulon. Intriguingly, in S. cerevisiae, the Ppr1 ortholog binds the same DNA motif (CGG(N6)CCG) as in C. albicans but serves as a regulator of pyrimidine biosynthesis. This transcription factor rewiring appears to have taken place at the same phylogenetic step as the formation of the rearranged DAL cluster. This transfer of the control of allantoin degradation from Ppr1 to Dal82, together with the repositioning of Ppr1 to the regulation of pyrimidine biosynthesis, may have resulted from a switch to a metabolism that could exploit hypoxic conditions in the lineage leading to N. castellii and S. cerevisiae.

PMID: 27321996 [PubMed - indexed for MEDLINE]