Literature DB >> 34471290

The polar oxy-metabolome reveals the 4-hydroxymandelate CoQ10 synthesis pathway.

Robert S Banh1,2, Esther S Kim1,2, Quentin Spillier1,2, Douglas E Biancur1,2, Keisuke Yamamoto1,2, Albert S W Sohn1,2, Guangbin Shi1,2, Drew R Jones3, Alec C Kimmelman1,2, Michael E Pacold4,5.   

Abstract

Oxygen is critical for a multitude of metabolic processes that are essential for human life. Biological processes can be identified by treating cells with 18O2 or other isotopically labelled gases and systematically identifying biomolecules incorporating labeled atoms. Here we labelled cell lines of distinct tissue origins with 18O2 to identify the polar oxy-metabolome, defined as polar metabolites labelled with 18O under different physiological O2 tensions. The most highly 18O-labelled feature was 4-hydroxymandelate (4-HMA). We demonstrate that 4-HMA is produced by hydroxyphenylpyruvate dioxygenase-like (HPDL), a protein of previously unknown function in human cells. We identify 4-HMA as an intermediate involved in the biosynthesis of the coenzyme Q10 (CoQ10) headgroup in human cells. The connection of HPDL to CoQ10 biosynthesis provides crucial insights into the mechanisms underlying recently described neurological diseases related to HPDL deficiencies1-4 and cancers with HPDL overexpression5.
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.

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Year:  2021        PMID: 34471290      PMCID: PMC8538427          DOI: 10.1038/s41586-021-03865-w

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   69.504


  36 in total

Review 1.  Oxygen and mammalian cell culture: are we repeating the experiment of Dr. Ox?

Authors:  Tslil Ast; Vamsi K Mootha
Journal:  Nat Metab       Date:  2019-09

2.  Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.

Authors:  Ralf A Husain; Mona Grimmel; Matias Wagner; J Christopher Hennings; Christian Marx; René G Feichtinger; Abdelkrim Saadi; Kevin Rostásy; Florentine Radelfahr; Andrea Bevot; Marion Döbler-Neumann; Hans Hartmann; Laurence Colleaux; Isabell Cordts; Xenia Kobeleva; Hossein Darvish; Somayeh Bakhtiari; Michael C Kruer; Arnaud Besse; Andy Cheuk-Him Ng; Diana Chiang; Francois Bolduc; Abbas Tafakhori; Shrikant Mane; Saghar Ghasemi Firouzabadi; Antje K Huebner; Rebecca Buchert; Stefanie Beck-Woedl; Amelie J Müller; Lucia Laugwitz; Thomas Nägele; Zhao-Qi Wang; Tim M Strom; Marc Sturm; Thomas Meitinger; Thomas Klockgether; Olaf Riess; Thomas Klopstock; Ulrich Brandl; Christian A Hübner; Marcus Deschauer; Johannes A Mayr; Penelope E Bonnen; Ingeborg Krägeloh-Mann; Saskia B Wortmann; Tobias B Haack
Journal:  Am J Hum Genet       Date:  2020-07-23       Impact factor: 11.025

Review 3.  4-Hydroxyphenylpyruvate dioxygenase.

Authors:  Graham R Moran
Journal:  Arch Biochem Biophys       Date:  2005-01-01       Impact factor: 4.013

4.  Characterization of the human prolyl 4-hydroxylases that modify the hypoxia-inducible factor.

Authors:  Maija Hirsilä; Peppi Koivunen; Volkmar Günzler; Kari I Kivirikko; Johanna Myllyharju
Journal:  J Biol Chem       Date:  2003-06-03       Impact factor: 5.157

5.  Fumarate and Succinate Regulate Expression of Hypoxia-inducible Genes via TET Enzymes.

Authors:  Tuomas Laukka; Christopher J Mariani; Tuukka Ihantola; John Z Cao; Juho Hokkanen; William G Kaelin; Lucy A Godley; Peppi Koivunen
Journal:  J Biol Chem       Date:  2015-12-23       Impact factor: 5.157

6.  Conserved N-terminal cysteine dioxygenases transduce responses to hypoxia in animals and plants.

Authors:  Norma Masson; Thomas P Keeley; Beatrice Giuntoli; Mark D White; Emily Flashman; Francesco Licausi; Peter J Ratcliffe; Mikel Lavilla Puerta; Pierdomenico Perata; Richard J Hopkinson
Journal:  Science       Date:  2019-07-05       Impact factor: 47.728

7.  Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvate dioxygenase-like protein, lead to an infantile neurodegenerative condition.

Authors:  Shereen G Ghosh; Sangmoon Lee; Rudy Fabunan; Guoliang Chai; Maha S Zaki; Ghada Abdel-Salam; Tipu Sultan; Tawfeg Ben-Omran; Javeria Raza Alvi; Jennifer McEvoy-Venneri; Valentina Stanley; Aakash Patel; Danica Ross; Jeffrey Ding; Mohit Jain; Daqiang Pan; Philipp Lübbert; Bernd Kammerer; Nils Wiedemann; Nanda M Verhoeven-Duif; Judith J Jans; David Murphy; Mehran Beiraghi Toosi; Farah Ashrafzadeh; Shima Imannezhad; Ehsan Ghayoor Karimiani; Khalid Ibrahim; Elizabeth R Waters; Reza Maroofian; Joseph G Gleeson
Journal:  Genet Med       Date:  2020-11-14       Impact factor: 8.822

8.  Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.

Authors:  Manuela Wiessner; Reza Maroofian; Meng-Yuan Ni; Andrea Pedroni; Juliane S Müller; Rolf Stucka; Christian Beetz; Stephanie Efthymiou; Filippo M Santorelli; Ahmed A Alfares; Changlian Zhu; Anna Uhrova Meszarosova; Elham Alehabib; Somayeh Bakhtiari; Andreas R Janecke; Maria Gabriela Otero; Jin Yun Helen Chen; James T Peterson; Tim M Strom; Peter De Jonghe; Tine Deconinck; Willem De Ridder; Jonathan De Winter; Rossella Pasquariello; Ivana Ricca; Majid Alfadhel; Bart P van de Warrenburg; Ruben Portier; Carsten Bergmann; Saghar Ghasemi Firouzabadi; Sheng Chih Jin; Kaya Bilguvar; Sherifa Hamed; Mohammed Abdelhameed; Nourelhoda A Haridy; Shazia Maqbool; Fatima Rahman; Najwa Anwar; Jenny Carmichael; Alistair Pagnamenta; Nick W Wood; Frederic Tran Mau-Them; Tobias Haack; Maja Di Rocco; Isabella Ceccherini; Michele Iacomino; Federico Zara; Vincenzo Salpietro; Marcello Scala; Marta Rusmini; Yiran Xu; Yinghong Wang; Yasuhiro Suzuki; Kishin Koh; Haitian Nan; Hiroyuki Ishiura; Shoji Tsuji; Laëtitia Lambert; Emmanuelle Schmitt; Elodie Lacaze; Hanna Küpper; David Dredge; Cara Skraban; Amy Goldstein; Mary J H Willis; Katheryn Grand; John M Graham; Richard A Lewis; Francisca Millan; Özgür Duman; Nihal Dündar; Gökhan Uyanik; Ludger Schöls; Peter Nürnberg; Gudrun Nürnberg; Andrea Catala Bordes; Pavel Seeman; Martin Kuchar; Hossein Darvish; Adriana Rebelo; Filipa Bouçanova; Jean-Jacques Medard; Roman Chrast; Michaela Auer-Grumbach; Fowzan S Alkuraya; Hanan Shamseldin; Saeed Al Tala; Jamileh Rezazadeh Varaghchi; Maryam Najafi; Selina Deschner; Dieter Gläser; Wolfgang Hüttel; Michael C Kruer; Erik-Jan Kamsteeg; Yoshihisa Takiyama; Stephan Züchner; Jonathan Baets; Matthis Synofzik; Rebecca Schüle; Rita Horvath; Henry Houlden; Luca Bartesaghi; Hwei-Jen Lee; Konstantinos Ampatzis; Tyler Mark Pierson; Jan Senderek
Journal:  Brain       Date:  2021-06-22       Impact factor: 13.501

Review 9.  The molecular machinery of regulated cell death.

Authors:  Daolin Tang; Rui Kang; Tom Vanden Berghe; Peter Vandenabeele; Guido Kroemer
Journal:  Cell Res       Date:  2019-04-04       Impact factor: 25.617

10.  Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL.

Authors:  Neil V Morgan; Bryndis Yngvadottir; Mary O'Driscoll; Graeme R Clark; Diana Walsh; Ezequiel Martin; Louise Tee; Evan Reid; Hannah L Titheradge; Eamonn R Maher
Journal:  Brain Commun       Date:  2021-01-28
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  2 in total

Review 1.  How plants synthesize coenzyme Q.

Authors:  Jing-Jing Xu; Mei Hu; Lei Yang; Xiao-Ya Chen
Journal:  Plant Commun       Date:  2022-05-25

2.  HPDL mutations identified by exome sequencing are associated with infant neurodevelopmental disorders.

Authors:  Yanhong Wang; Xuan Zheng; Chao Feng; Xiaoge Fan; Lei Liu; Pengbo Guo; Zhi Lei; Shiyue Mei
Journal:  Mol Genet Genomic Med       Date:  2022-08-19       Impact factor: 2.473

  2 in total

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