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      Metabolic Enzymes Enjoying New Partnerships as RNA-Binding Proteins

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          Abstract

          In the past century, few areas of biology advanced as much as our understanding of the pathways of intermediary metabolism. Initially considered unimportant in terms of gene regulation, crucial cellular fate changes, cell differentiation, or malignant transformation are now known to involve ‘metabolic remodeling’ with profound changes in the expression of many metabolic enzyme genes. This review focuses on the recent identification of RNA-binding activity of numerous metabolic enzymes. We discuss possible roles of this unexpected second activity in feedback gene regulation (‘moonlighting’) and/or in the control of enzymatic function. We also consider how metabolism-driven post-translational modifications could regulate enzyme–RNA interactions. Thus, RNA emerges as a new partner of metabolic enzymes with far-reaching possible consequences to be unraveled in the future.

          Trends

          Genetic control of metabolism is currently best understood at the level of transcription and epigenetics. Only limited information is available on post-transcriptional regulation of metabolism.

          While a few metabolic enzymes were previously known to moonlight as RNA-binding proteins in physiologically relevant contexts, recent discoveries highlight that several dozen of metabolic enzymes belonging to a wide spectrum of pathways exhibit RNA-binding activity in living mammalian cells.

          Abundant RNA–enzyme interactions might suggest novel roles of RNA in affecting enzyme function, for instance, as competitive inhibitors or allosteric regulators. A function of RNA as assembly scaffold for enzyme complexes is also conceivable, with potentially wide-ranging implications for our understanding of how cells organize and control metabolic flux. Finally, enzymes can moonlight as regulators of (m)RNAs, as exemplified by aconitase/IRP1 and GAPDH.

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          Most cited references74

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          The nuclear receptor superfamily: the second decade.

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            RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme.

            tRNAs are synthesized as immature precursors, and on their way to functional maturity, extra nucleotides at their 5' ends are removed by an endonuclease called RNase P. All RNase P enzymes characterized so far are composed of an RNA plus one or more proteins, and tRNA 5' end maturation is considered a universal ribozyme-catalyzed process. Using a combinatorial purification/proteomics approach, we identified the components of human mitochondrial RNase P and reconstituted the enzymatic activity from three recombinant proteins. We thereby demonstrate that human mitochondrial RNase P is a protein enzyme that does not require a trans-acting RNA component for catalysis. Moreover, the mitochondrial enzyme turns out to be an unexpected type of patchwork enzyme, composed of a tRNA methyltransferase, a short-chain dehydrogenase/reductase-family member, and a protein of hitherto unknown functional and evolutionary origin, possibly representing the enzyme's metallonuclease moiety. Apparently, animal mitochondria lost the seemingly ubiquitous RNA world remnant after reinventing RNase P from preexisting components.
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              The RNA-binding protein repertoire of embryonic stem cells.

              RNA-binding proteins (RBPs) have essential roles in RNA-mediated gene regulation, and yet annotation of RBPs is limited mainly to those with known RNA-binding domains. To systematically identify the RBPs of embryonic stem cells (ESCs), we here employ interactome capture, which combines UV cross-linking of RBP to RNA in living cells, oligo(dT) capture and MS. From mouse ESCs (mESCs), we have defined 555 proteins constituting the mESC mRNA interactome, including 283 proteins not previously annotated as RBPs. Of these, 68 new RBP candidates are highly expressed in ESCs compared to differentiated cells, implicating a role in stem-cell physiology. Two well-known E3 ubiquitin ligases, Trim25 (also called Efp) and Trim71 (also called Lin41), are validated as RBPs, revealing a potential link between RNA biology and protein-modification pathways. Our study confirms and expands the atlas of RBPs, providing a useful resource for the study of the RNA-RBP network in stem cells.

                Author and article information

                Contributors
                Journal
                Trends Endocrinol Metab
                Trends Endocrinol. Metab
                Trends in Endocrinology and Metabolism
                Elsevier Science Pub. Co
                1043-2760
                1879-3061
                1 December 2015
                December 2015
                : 26
                : 12
                : 746-757
                Affiliations
                [1 ]Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK
                [2 ]European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany
                [3 ]EMBL–Australia Collaborating Group, Department of Genome Sciences, The John Curtin School of Medical Research, The Australian National University, Acton (Canberra), ACT 2601, Australia
                [4 ]Victor Chang Cardiac Research Institute, Darlinghurst (Sydney), New South Wales 2010, Australia
                Author notes
                [* ]Correspondence: hentze@ 123456embl.de
                Article
                S1043-2760(15)00195-2
                10.1016/j.tem.2015.09.012
                4671484
                26520658
                246cd7c0-7538-4c53-9f52-5905a2fe708d
                © 2015 Elsevier Ltd. All rights reserved.

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                Categories
                Review
                Special Issue: Systems Approach to Metabolic Disease

                Endocrinology & Diabetes
                metabolic enzymes,metabolon,rna,rna-binding proteins,post-transcriptional regulation,post-translational modifications

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