IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-36210-y.html
   My bibliography  Save this article

A paralog of Pcc1 is the fifth core subunit of the KEOPS tRNA-modifying complex in Archaea

Author

Listed:
  • Marie-Claire Daugeron

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC))

  • Sophia Missoury

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC)
    Institut Pasteur)

  • Violette Cunha

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC)
    Univ Evry, Université Paris-Saclay)

  • Noureddine Lazar

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC))

  • Bruno Collinet

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC)
    Institut de Minéralogie de Physique des Matériaux et de Cosmochimie (IMPMC), Sorbonne-Université, UMR7590 CNRS, MNHN)

  • Herman Tilbeurgh

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC))

  • Tamara Basta

    (Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC))

Abstract

In Archaea and Eukaryotes, the synthesis of a universal tRNA modification, N6-threonyl-carbamoyl adenosine (t6A), is catalyzed by the KEOPS complex composed of Kae1, Bud32, Cgi121, and Pcc1. A fifth subunit, Gon7, is found only in Fungi and Metazoa. Here, we identify and characterize a fifth KEOPS subunit in Archaea. This protein, dubbed Pcc2, is a paralog of Pcc1 and is widely conserved in Archaea. Pcc1 and Pcc2 form a heterodimer in solution, and show modest sequence conservation but very high structural similarity. The five-subunit archaeal KEOPS does not form dimers but retains robust tRNA binding and t6A synthetic activity. Pcc2 can substitute for Pcc1 but the resulting KEOPS complex is inactive, suggesting a distinct function for the two paralogs. Comparative sequence and structure analyses point to a possible evolutionary link between archaeal Pcc2 and eukaryotic Gon7. Our work indicates that Pcc2 regulates the oligomeric state of the KEOPS complex, a feature that seems to be conserved from Archaea to Eukaryotes.

Suggested Citation

  • Marie-Claire Daugeron & Sophia Missoury & Violette Cunha & Noureddine Lazar & Bruno Collinet & Herman Tilbeurgh & Tamara Basta, 2023. "A paralog of Pcc1 is the fifth core subunit of the KEOPS tRNA-modifying complex in Archaea," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36210-y
    DOI: 10.1038/s41467-023-36210-y
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-36210-y
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-36210-y?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Changyi Zhang & Alex P. R. Phillips & Rebecca L. Wipfler & Gary J. Olsen & Rachel J. Whitaker, 2018. "The essential genome of the crenarchaeal model Sulfolobus islandicus," Nature Communications, Nature, vol. 9(1), pages 1-11, December.
    2. F. Lemoine & J.-B. Domelevo Entfellner & E. Wilkinson & D. Correia & M. Dávila Felipe & T. Oliveira & O. Gascuel, 2018. "Renewing Felsenstein’s phylogenetic bootstrap in the era of big data," Nature, Nature, vol. 556(7702), pages 452-456, April.
    3. Jonah Beenstock & Samara Mishelle Ona & Jennifer Porat & Stephen Orlicky & Leo C. K. Wan & Derek F. Ceccarelli & Pierre Maisonneuve & Rachel K. Szilard & Zhe Yin & Dheva Setiaputra & Daniel Y. L. Mao , 2020. "A substrate binding model for the KEOPS tRNA modifying complex," Nature Communications, Nature, vol. 11(1), pages 1-17, December.
    4. Christelle Arrondel & Sophia Missoury & Rozemarijn Snoek & Julie Patat & Giulia Menara & Bruno Collinet & Dominique Liger & Dominique Durand & Olivier Gribouval & Olivia Boyer & Laurine Buscara & Gaël, 2019. "Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Michael P. Andreas & Tobias W. Giessen, 2024. "The biosynthesis of the odorant 2-methylisoborneol is compartmentalized inside a protein shell," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    2. Matthew Goulty & Gaelle Botton-Amiot & Ezio Rosato & Simon G. Sprecher & Roberto Feuda, 2023. "The monoaminergic system is a bilaterian innovation," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    3. Octavio R. Salazar & Ke Chen & Vanessa J. Melino & Muppala P. Reddy & Eva Hřibová & Jana Čížková & Denisa Beránková & Juan Pablo Arciniegas Vega & Lina María Cáceres Leal & Manuel Aranda & Lukasz Jare, 2024. "SOS1 tonoplast neo-localization and the RGG protein SALTY are important in the extreme salinity tolerance of Salicornia bigelovii," Nature Communications, Nature, vol. 15(1), pages 1-21, December.
    4. Aline Umuhire Juru & Rodolfo Ghirlando & Jinwei Zhang, 2024. "Structural basis of tRNA recognition by the widespread OB fold," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    5. Fabian Blombach & Michal Sýkora & Jo Case & Xu Feng & Diana P. Baquero & Thomas Fouqueau & Duy Khanh Phung & Declan Barker & Mart Krupovic & Qunxin She & Finn Werner, 2024. "Cbp1 and Cren7 form chromatin-like structures that ensure efficient transcription of long CRISPR arrays," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    6. Ya Gao & Daisylyn Senna Tan & Mathias Girbig & Haoqing Hu & Xiaomin Zhou & Qianwen Xie & Shi Wing Yeung & Kin Shing Lee & Sik Yin Ho & Vlad Cojocaru & Jian Yan & Georg K. A. Hochberg & Alex Mendoza & , 2024. "The emergence of Sox and POU transcription factors predates the origins of animal stem cells," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    7. Alessandro Boverio & Neelam Jamil & Barbara Mannucci & Maria Laura Mascotti & Marco W. Fraaije & Andrea Mattevi, 2024. "Structure, mechanism, and evolution of the last step in vitamin C biosynthesis," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    8. Yuvaraj Bhoobalan-Chitty & Shuanshuan Xu & Laura Martinez-Alvarez & Svetlana Karamycheva & Kira S. Makarova & Eugene V. Koonin & Xu Peng, 2024. "Regulatory sequence-based discovery of anti-defense genes in archaeal viruses," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    9. Joao A. Ascensao & Kelly M. Wetmore & Benjamin H. Good & Adam P. Arkin & Oskar Hallatschek, 2023. "Quantifying the local adaptive landscape of a nascent bacterial community," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    10. Gautier Bailleul & Guang Yang & Callum R. Nicoll & Andrea Mattevi & Marco W. Fraaije & Maria Laura Mascotti, 2023. "Evolution of enzyme functionality in the flavin-containing monooxygenases," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    11. Fares Boudjouan & Walid Zeghbib & João Carneiro & Raquel Silva & João Morais & Vitor Vasconcelos & Graciliana Lopes, 2022. "Comparison Study on Wild and Cultivated Opuntia sp.: Chemical, Taxonomic, and Antioxidant Evaluations," Agriculture, MDPI, vol. 12(11), pages 1-21, October.
    12. Tomoyuki Hatano & Saravanan Palani & Dimitra Papatziamou & Ralf Salzer & Diorge P. Souza & Daniel Tamarit & Mehul Makwana & Antonia Potter & Alexandra Haig & Wenjue Xu & David Townsend & David Rochest, 2022. "Asgard archaea shed light on the evolutionary origins of the eukaryotic ubiquitin-ESCRT machinery," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    13. Heather R. Kates & Brian C. O’Meara & Raphael LaFrance & Gregory W. Stull & Euan K. James & Shui-Yin Liu & Qin Tian & Ting-Shuang Yi & Daniel Conde & Matias Kirst & Jean-Michel Ané & Douglas E. Soltis, 2024. "Shifts in evolutionary lability underlie independent gains and losses of root-nodule symbiosis in a single clade of plants," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36210-y. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.