Literature DB >> 18322039

Moonlighting proteins in yeasts.

Carlos Gancedo1, Carmen-Lisset Flores.   

Abstract

Proteins able to participate in unrelated biological processes have been grouped under the generic name of moonlighting proteins. Work with different yeast species has uncovered a great number of moonlighting proteins and shown their importance for adequate functioning of the yeast cell. Moonlighting activities in yeasts include such diverse functions as control of gene expression, organelle assembly, and modification of the activity of metabolic pathways. In this review, we consider several well-studied moonlighting proteins in different yeast species, paying attention to the experimental approaches used to identify them and the evidence that supports their participation in the unexpected function. Usually, moonlighting activities have been uncovered unexpectedly, and up to now, no satisfactory way to predict moonlighting activities has been found. Among the well-characterized moonlighting proteins in yeasts, enzymes from the glycolytic pathway appear to be prominent. For some cases, it is shown that despite close phylogenetic relationships, moonlighting activities are not necessarily conserved among yeast species. Organisms may utilize moonlighting to add a new layer of regulation to conventional regulatory networks. The existence of this type of proteins in yeasts should be taken into account when designing mutant screens or in attempts to model or modify yeast metabolism.

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Year:  2008        PMID: 18322039      PMCID: PMC2268286          DOI: 10.1128/MMBR.00036-07

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  146 in total

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Authors:  O Zelenaya-Troitskaya; P S Perlman; R A Butow
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  58 in total

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Review 8.  The Expanding Landscape of Moonlighting Proteins in Yeasts.

Authors:  Carlos Gancedo; Carmen-Lisset Flores; Juana M Gancedo
Journal:  Microbiol Mol Biol Rev       Date:  2016-07-27       Impact factor: 11.056

9.  Glyceraldehyde 3-phosphate dehydrogenase depletion induces cell cycle arrest and resistance to antimetabolites in human carcinoma cell lines.

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