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The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)

Nocturnin (NOCT) is a rhythmically expressed protein that regulates metabolism under the control of circadian clock. It has been proposed that NOCT deadenylates and regulates metabolic enzyme mRNAs. However, in contrast to other deadenylases, purified NOCT lacks the deadenylase activity. To identify...

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Autores principales: Estrella, Michael A., Du, Jin, Chen, Li, Rath, Sneha, Prangley, Eliza, Chitrakar, Alisha, Aoki, Tsutomu, Schedl, Paul, Rabinowitz, Joshua, Korennykh, Alexei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542800/
https://www.ncbi.nlm.nih.gov/pubmed/31147539
http://dx.doi.org/10.1038/s41467-019-10125-z
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author Estrella, Michael A.
Du, Jin
Chen, Li
Rath, Sneha
Prangley, Eliza
Chitrakar, Alisha
Aoki, Tsutomu
Schedl, Paul
Rabinowitz, Joshua
Korennykh, Alexei
author_facet Estrella, Michael A.
Du, Jin
Chen, Li
Rath, Sneha
Prangley, Eliza
Chitrakar, Alisha
Aoki, Tsutomu
Schedl, Paul
Rabinowitz, Joshua
Korennykh, Alexei
author_sort Estrella, Michael A.
collection PubMed
description Nocturnin (NOCT) is a rhythmically expressed protein that regulates metabolism under the control of circadian clock. It has been proposed that NOCT deadenylates and regulates metabolic enzyme mRNAs. However, in contrast to other deadenylases, purified NOCT lacks the deadenylase activity. To identify the substrate of NOCT, we conducted a mass spectrometry screen and report that NOCT specifically and directly converts the dinucleotide NADP(+) into NAD(+) and NADPH into NADH. Further, we demonstrate that the Drosophila NOCT ortholog, Curled, has the same enzymatic activity. We obtained the 2.7 Å crystal structure of the human NOCT•NADPH complex, which revealed that NOCT recognizes the chemically unique ribose-phosphate backbone of the metabolite, placing the 2′-terminal phosphate productively for removal. We provide evidence for NOCT targeting to mitochondria and propose that NADP(H) regulation, which takes place at least in part in mitochondria, establishes the molecular link between circadian clock and metabolism.
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spelling pubmed-65428002019-06-03 The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled) Estrella, Michael A. Du, Jin Chen, Li Rath, Sneha Prangley, Eliza Chitrakar, Alisha Aoki, Tsutomu Schedl, Paul Rabinowitz, Joshua Korennykh, Alexei Nat Commun Article Nocturnin (NOCT) is a rhythmically expressed protein that regulates metabolism under the control of circadian clock. It has been proposed that NOCT deadenylates and regulates metabolic enzyme mRNAs. However, in contrast to other deadenylases, purified NOCT lacks the deadenylase activity. To identify the substrate of NOCT, we conducted a mass spectrometry screen and report that NOCT specifically and directly converts the dinucleotide NADP(+) into NAD(+) and NADPH into NADH. Further, we demonstrate that the Drosophila NOCT ortholog, Curled, has the same enzymatic activity. We obtained the 2.7 Å crystal structure of the human NOCT•NADPH complex, which revealed that NOCT recognizes the chemically unique ribose-phosphate backbone of the metabolite, placing the 2′-terminal phosphate productively for removal. We provide evidence for NOCT targeting to mitochondria and propose that NADP(H) regulation, which takes place at least in part in mitochondria, establishes the molecular link between circadian clock and metabolism. Nature Publishing Group UK 2019-05-30 /pmc/articles/PMC6542800/ /pubmed/31147539 http://dx.doi.org/10.1038/s41467-019-10125-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Estrella, Michael A.
Du, Jin
Chen, Li
Rath, Sneha
Prangley, Eliza
Chitrakar, Alisha
Aoki, Tsutomu
Schedl, Paul
Rabinowitz, Joshua
Korennykh, Alexei
The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)
title The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)
title_full The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)
title_fullStr The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)
title_full_unstemmed The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)
title_short The metabolites NADP(+) and NADPH are the targets of the circadian protein Nocturnin (Curled)
title_sort metabolites nadp(+) and nadph are the targets of the circadian protein nocturnin (curled)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6542800/
https://www.ncbi.nlm.nih.gov/pubmed/31147539
http://dx.doi.org/10.1038/s41467-019-10125-z
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