IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-43263-6.html
   My bibliography  Save this article

A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei

Author

Listed:
  • K. Shanmugha Rajan

    (Bar-Ilan University
    Weizmann Institute of Science)

  • Hava Madmoni

    (Bar-Ilan University)

  • Anat Bashan

    (Weizmann Institute of Science)

  • Masato Taoka

    (Tokyo Metropolitan University)

  • Saurav Aryal

    (Bar-Ilan University)

  • Yuko Nobe

    (Tokyo Metropolitan University)

  • Tirza Doniger

    (Bar-Ilan University)

  • Beathrice Galili Kostin

    (Bar-Ilan University)

  • Amit Blumberg

    (Tokyo Metropolitan University)

  • Smadar Cohen-Chalamish

    (Bar-Ilan University)

  • Schraga Schwartz

    (Weizmann Institute of Science)

  • Andre Rivalta

    (Weizmann Institute of Science)

  • Ella Zimmerman

    (Weizmann Institute of Science)

  • Ron Unger

    (Bar-Ilan University)

  • Toshiaki Isobe

    (Tokyo Metropolitan University)

  • Ada Yonath

    (Weizmann Institute of Science)

  • Shulamit Michaeli

    (Bar-Ilan University)

Abstract

Trypanosomes are protozoan parasites that cycle between insect and mammalian hosts and are the causative agent of sleeping sickness. Here, we describe the changes of pseudouridine (Ψ) modification on rRNA in the two life stages of the parasite using four different genome-wide approaches. CRISPR-Cas9 knock-outs of all four snoRNAs guiding Ψ on helix 69 (H69) of the large rRNA subunit were lethal. A single knock-out of a snoRNA guiding Ψ530 on H69 altered the composition of the 80S monosome. These changes specifically affected the translation of only a subset of proteins. This study correlates a single site Ψ modification with changes in ribosomal protein stoichiometry, supported by a high-resolution cryo-EM structure. We propose that alteration in rRNA modifications could generate ribosomes preferentially translating state-beneficial proteins.

Suggested Citation

  • K. Shanmugha Rajan & Hava Madmoni & Anat Bashan & Masato Taoka & Saurav Aryal & Yuko Nobe & Tirza Doniger & Beathrice Galili Kostin & Amit Blumberg & Smadar Cohen-Chalamish & Schraga Schwartz & Andre , 2023. "A single pseudouridine on rRNA regulates ribosome structure and function in the mammalian parasite Trypanosoma brucei," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43263-6
    DOI: 10.1038/s41467-023-43263-6
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-43263-6
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-43263-6?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. Moran Shalev-Benami & Yan Zhang & Haim Rozenberg & Yuko Nobe & Masato Taoka & Donna Matzov & Ella Zimmerman & Anat Bashan & Toshiaki Isobe & Charles L. Jaffe & Ada Yonath & Georgios Skiniotis, 2017. "Atomic resolution snapshot of Leishmania ribosome inhibition by the aminoglycoside paromomycin," Nature Communications, Nature, vol. 8(1), pages 1-9, December.
    2. Heena Khatter & Alexander G. Myasnikov & S. Kundhavai Natchiar & Bruno P. Klaholz, 2015. "Structure of the human 80S ribosome," Nature, Nature, vol. 520(7549), pages 640-645, April.
    3. Yaser Hashem & Amedee des Georges & Jie Fu & Sarah N. Buss & Fabrice Jossinet & Amy Jobe & Qin Zhang & Hstau Y. Liao & Robert A. Grassucci & Chandrajit Bajaj & Eric Westhof & Susan Madison-Antenucci &, 2013. "High-resolution cryo-electron microscopy structure of the Trypanosoma brucei ribosome," Nature, Nature, vol. 494(7437), pages 385-389, February.
    4. Alexey Rozov & Iskander Khusainov & Kamel El Omari & Ramona Duman & Vitaliy Mykhaylyk & Marat Yusupov & Eric Westhof & Armin Wagner & Gulnara Yusupova, 2019. "Importance of potassium ions for ribosome structure and function revealed by long-wavelength X-ray diffraction," Nature Communications, Nature, vol. 10(1), pages 1-12, December.
    5. Aldema Sas-Chen & Justin M. Thomas & Donna Matzov & Masato Taoka & Kellie D. Nance & Ronit Nir & Keri M. Bryson & Ran Shachar & Geraldy L. S. Liman & Brett W. Burkhart & Supuni Thalalla Gamage & Yuko , 2020. "Dynamic RNA acetylation revealed by quantitative cross-evolutionary mapping," Nature, Nature, vol. 583(7817), pages 638-643, July.
    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 F. Fuss & Jan-Philip Wieferig & Robin A. Corey & Yvonne Hellmich & Igor Tascón & Joana S. Sousa & Phillip J. Stansfeld & Janet Vonck & Inga Hänelt, 2023. "Cyclic di-AMP traps proton-coupled K+ transporters of the KUP family in an inward-occluded conformation," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Casper Berger & Maud Dumoux & Thomas Glen & Neville B.-y. Yee & John M. Mitchels & Zuzana Patáková & Michele C. Darrow & James H. Naismith & Michael Grange, 2023. "Plasma FIB milling for the determination of structures in situ," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    3. Gabriel Therizols & Zeina Bash-Imam & Baptiste Panthu & Christelle Machon & Anne Vincent & Julie Ripoll & Sophie Nait-Slimane & Mounira Chalabi-Dchar & Angéline Gaucherot & Maxime Garcia & Florian Laf, 2022. "Alteration of ribosome function upon 5-fluorouracil treatment favors cancer cell drug-tolerance," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    4. Belinda Baquero-Pérez & Ivaylo D. Yonchev & Anna Delgado-Tejedor & Rebeca Medina & Mireia Puig-Torrents & Ian Sudbery & Oguzhan Begik & Stuart A. Wilson & Eva Maria Novoa & Juana Díez, 2024. "N6-methyladenosine modification is not a general trait of viral RNA genomes," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    5. Jianheng Liu & Tao Huang & Wanying Chen & Chenhui Ding & Tianxuan Zhao & Xueni Zhao & Bing Cai & Yusen Zhang & Song Li & Ling Zhang & Maoguang Xue & Xiuju He & Wanzhong Ge & Canquan Zhou & Yanwen Xu &, 2022. "Developmental mRNA m5C landscape and regulatory innovations of massive m5C modification of maternal mRNAs in animals," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    6. Simon A. Fromm & Kate M. O’Connor & Michael Purdy & Pramod R. Bhatt & Gary Loughran & John F. Atkins & Ahmad Jomaa & Simone Mattei, 2023. "The translating bacterial ribosome at 1.55 Å resolution generated by cryo-EM imaging services," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    7. Florent Waltz & Thalia Salinas-Giegé & Robert Englmeier & Herrade Meichel & Heddy Soufari & Lauriane Kuhn & Stefan Pfeffer & Friedrich Förster & Benjamin D. Engel & Philippe Giegé & Laurence Drouard &, 2021. "How to build a ribosome from RNA fragments in Chlamydomonas mitochondria," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    8. Dylan Girodat & Hans-Joachim Wieden & Scott C. Blanchard & Karissa Y. Sanbonmatsu, 2023. "Geometric alignment of aminoacyl-tRNA relative to catalytic centers of the ribosome underpins accurate mRNA decoding," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    9. Qin Yan & Jing Zhou & Ziyu Wang & Xiangya Ding & Xinyue Ma & Wan Li & Xuemei Jia & Shou-Jiang Gao & Chun Lu, 2023. "NAT10-dependent N4‐acetylcytidine modification mediates PAN RNA stability, KSHV reactivation, and IFI16-related inflammasome activation," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    10. Nozomi Takahashi & Federica Franciosi & Enrico Maria Daldello & Xuan G. Luong & Peter Althoff & Xiaotian Wang & Marco Conti, 2023. "CPEB1-dependent disruption of the mRNA translation program in oocytes during maternal aging," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
    11. Chengwei Zeng & Yiren Jian & Soroush Vosoughi & Chen Zeng & Yunjie Zhao, 2023. "Evaluating native-like structures of RNA-protein complexes through the deep learning method," Nature Communications, Nature, vol. 14(1), pages 1-9, December.
    12. Jana Aupič & Jure Borišek & Sebastian M. Fica & Wojciech P. Galej & Alessandra Magistrato, 2023. "Monovalent metal ion binding promotes the first transesterification reaction in the spliceosome," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    13. Victor Tobiasson & Ieva Berzina & Alexey Amunts, 2022. "Structure of a mitochondrial ribosome with fragmented rRNA in complex with membrane-targeting elements," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    14. Haonan Zhang & Yan Li & Yanan Liu & Dongyu Li & Lin Wang & Kai Song & Keyan Bao & Ping Zhu, 2023. "A method for restoring signals and revealing individual macromolecule states in cryo-ET, REST," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    15. Xue Jiang & Yu Cheng & Yuzhang Zhu & Caoling Xu & Qiaodan Li & Xuemei Xing & Wenqing Li & Jiaqi Zou & Lan Meng & Muhammad Azhar & Yuzhu Cao & Xianhong Tong & Weibing Qin & Xiaoli Zhu & Jianqiang Bao, 2023. "Maternal NAT10 orchestrates oocyte meiotic cell-cycle progression and maturation in mice," Nature Communications, Nature, vol. 14(1), pages 1-23, 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_s41467-023-43263-6. 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.