Literature DB >> 30529455

The emerging impact of tRNA modifications in the brain and nervous system.

Jillian Ramos1, Dragony Fu2.   

Abstract

A remarkable number of neurodevelopmental disorders have been linked to defects in tRNA modifications. These discoveries place tRNA modifications in the spotlight as critical modulators of gene expression pathways that are required for proper organismal growth and development. Here, we discuss the emerging molecular and cellular functions of the diverse tRNA modifications linked to cognitive and neurological disorders. In particular, we describe how the structure and location of a tRNA modification influences tRNA folding, stability, and function. We then highlight how modifications in tRNA can impact multiple aspects of protein translation that are instrumental for maintaining proper cellular proteostasis. Importantly, we describe how perturbations in tRNA modification lead to a spectrum of deleterious biological outcomes that can disturb neurodevelopment and neurological function. Finally, we summarize the biological themes shared by the different tRNA modifications linked to cognitive disorders and offer insight into the future questions that remain to decipher the role of tRNA modifications. This article is part of a Special Issue entitled: mRNA modifications in gene expression control edited by Dr. Soller Matthias and Dr. Fray Rupert.
Copyright © 2018 Elsevier B.V. All rights reserved.

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Year:  2018        PMID: 30529455     DOI: 10.1016/j.bbagrm.2018.11.007

Source DB:  PubMed          Journal:  Biochim Biophys Acta Gene Regul Mech        ISSN: 1874-9399            Impact factor:   4.490


  12 in total

1.  PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly.

Authors:  Ranad Shaheen; Monika Tasak; Sateesh Maddirevula; Ghada M H Abdel-Salam; Inas S M Sayed; Anas M Alazami; Tarfa Al-Sheddi; Eman Alobeid; Eric M Phizicky; Fowzan S Alkuraya
Journal:  Hum Genet       Date:  2019-02-18       Impact factor: 4.132

2.  THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder.

Authors:  Martin Broly; Bogdan V Polevoda; Kamel M Awayda; Ning Tong; Jenna Lentini; Thomas Besnard; Wallid Deb; Declan O'Rourke; Julia Baptista; Sian Ellard; Mohammed Almannai; Mais Hashem; Ferdous Abdulwahab; Hanan Shamseldin; Saeed Al-Tala; Fowzan S Alkuraya; Alberta Leon; Rosa L E van Loon; Alessandra Ferlini; Mariabeatrice Sanchini; Stefania Bigoni; Andrea Ciorba; Hans van Bokhoven; Zafar Iqbal; Almundher Al-Maawali; Fathiya Al-Murshedi; Anuradha Ganesh; Watfa Al-Mamari; Sze Chern Lim; Lynn S Pais; Natasha Brown; Saima Riazuddin; Stéphane Bézieau; Dragony Fu; Bertrand Isidor; Benjamin Cogné; Mitchell R O'Connell
Journal:  Am J Hum Genet       Date:  2022-02-22       Impact factor: 11.043

3.  An intellectual disability-associated missense variant in TRMT1 impairs tRNA modification and reconstitution of enzymatic activity.

Authors:  Kejia Zhang; Jenna M Lentini; Christopher T Prevost; Mais O Hashem; Fowzan S Alkuraya; Dragony Fu
Journal:  Hum Mutat       Date:  2020-01-16       Impact factor: 4.878

4.  Identification of the 3-amino-3-carboxypropyl (acp) transferase enzyme responsible for acp3U formation at position 47 in Escherichia coli tRNAs.

Authors:  Britta Meyer; Carina Immer; Steffen Kaiser; Sunny Sharma; Jun Yang; Peter Watzinger; Lena Weiß; Annika Kotter; Mark Helm; Hans-Michael Seitz; Peter Kötter; Stefanie Kellner; Karl-Dieter Entian; Jens Wöhnert
Journal:  Nucleic Acids Res       Date:  2020-02-20       Impact factor: 16.971

Review 5.  The expanding world of tRNA modifications and their disease relevance.

Authors:  Tsutomu Suzuki
Journal:  Nat Rev Mol Cell Biol       Date:  2021-03-03       Impact factor: 94.444

6.  Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene.

Authors:  Chengcheng Zhang; Xiaojing Li; Liansheng Zhao; Rong Liang; Wei Deng; Wanjun Guo; Qiang Wang; Xun Hu; Xiangdong Du; Pak Chung Sham; Xiongjian Luo; Tao Li
Journal:  BMC Med       Date:  2022-05-09       Impact factor: 11.150

7.  Biogenesis and functions of aminocarboxypropyluridine in tRNA.

Authors:  Mayuko Takakura; Kensuke Ishiguro; Shinichiro Akichika; Kenjyo Miyauchi; Tsutomu Suzuki
Journal:  Nat Commun       Date:  2019-12-05       Impact factor: 14.919

8.  Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome.

Authors:  Christelle Arrondel; Sophia Missoury; Rozemarijn Snoek; Julie Patat; Giulia Menara; Bruno Collinet; Dominique Liger; Dominique Durand; Olivier Gribouval; Olivia Boyer; Laurine Buscara; Gaëlle Martin; Eduardo Machuca; Fabien Nevo; Ewen Lescop; Daniela A Braun; Anne-Claire Boschat; Sylvia Sanquer; Ida Chiara Guerrera; Patrick Revy; Mélanie Parisot; Cécile Masson; Nathalie Boddaert; Marina Charbit; Stéphane Decramer; Robert Novo; Marie-Alice Macher; Bruno Ranchin; Justine Bacchetta; Audrey Laurent; Sophie Collardeau-Frachon; Albertien M van Eerde; Friedhelm Hildebrandt; Daniella Magen; Corinne Antignac; Herman van Tilbeurgh; Géraldine Mollet
Journal:  Nat Commun       Date:  2019-09-03       Impact factor: 14.919

9.  Loss of Ftsj1 perturbs codon-specific translation efficiency in the brain and is associated with X-linked intellectual disability.

Authors:  Y Nagayoshi; T Chujo; S Hirata; H Nakatsuka; C-W Chen; M Takakura; K Miyauchi; Y Ikeuchi; B C Carlyle; R R Kitchen; T Suzuki; F Katsuoka; M Yamamoto; Y Goto; M Tanaka; K Natsume; A C Nairn; T Suzuki; K Tomizawa; F-Y Wei
Journal:  Sci Adv       Date:  2021-03-26       Impact factor: 14.136

10.  Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder.

Authors:  Jillian Ramos; Melissa Proven; Jonatan Halvardson; Felix Hagelskamp; Ekaterina Kuchinskaya; Benjamin Phelan; Ryan Bell; Stefanie M Kellner; Lars Feuk; Ann-Charlotte Thuresson; Dragony Fu
Journal:  RNA       Date:  2020-08-06       Impact factor: 4.942

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