PUBLICATION

Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

Authors
Efthymiou, S., Leo, C.P., Deng, C., Lin, S.J., Maroofian, R., Lin, R., Karagoz, I., Zhang, K., Kaiyrzhanov, R., Scardamaglia, A., Owrang, D., Turchetti, V., Jahnke, F., Huang, K., Petree, C., Derrick, A.V., Rees, M.I., Alvi, J.R., Sultan, T., Li, C., Jacquemont, M.L., Tran-Mau-Them, F., Valenzuela-Palafoll, M., Sidlow, R., Yoon, G., Morrow, M.M., Carere, D.A., O'Connor, M., Fleischer, J., Gerkes, E.H., Phornphutkul, C., Isidor, B., Rivier-Ringenbach, C., Philippe, C., Kurul, S.H., Soydemir, D., Kara, B., Sunnetci-Akkoyunlu, D., Bothe, V., Platzer, K., Wieczorek, D., Koch-Hogrebe, M., Rahner, N., Thuresson, A.C., Matsson, H., Frykholm, C., Bozdoğan, S.T., Bisgin, A., Chatron, N., Lesca, G., Cabet, S., Tümer, Z., Hjortshøj, T.D., Rønde, G., Marquardt, T., Reunert, J., Afzal, E., Zamani, M., Azizimalamiri, R., Galehdari, H., Nourbakhsh, P., Chamanrou, N., Chung, S.K., Suri, M., Benke, P.J., Zaki, M.S., Gleeson, J.G., Calame, D.G., Pehlivan, D., Yilmaz, H.I., Gezdirici, A., Rad, A., Abumansour, I.S., Oprea, G., Bereketoğlu, M.B., Banneau, G., Julia, S., Zeighami, J., Ashoori, S., Shariati, G., Sedaghat, A., Sabri, A., Hamid, M., Parvas, S., Tajudin, T.A., Abdullah, U., Baig, S.M., Chung, W.K., Glazunova, O.O., Sabine, S., Cheema, H.A., Zifarelli, G., Bauer, P., Sidpra, J., Mankad, K., Vona, B., Fry, A.E., Varshney, G.K., Houlden, H., Fu, D.
ID
ZDB-PUB-250418-10
Date
2025
Source
American journal of human genetics : (Journal)
Registered Authors
Lin, Sheng-Jia, Varshney, Gaurav
Keywords
TRMT1, disease model, intellectual disability, neurodevelopmental disorder, tRNA modification, zebrafish
MeSH Terms
  • Female
  • RNA Processing, Post-Transcriptional/genetics
  • Humans
  • Neurodevelopmental Disorders*/genetics
  • Neurodevelopmental Disorders*/pathology
  • Alleles
  • Male
  • Child
  • tRNA Methyltransferases*/genetics
  • tRNA Methyltransferases*/metabolism
  • Child, Preschool
  • RNA, Transfer*/genetics
  • RNA, Transfer*/metabolism
  • Adolescent
  • Zebrafish/genetics
  • Animals
  • Intellectual Disability/genetics
PubMed
40245862 Full text @ Am. J. Hum. Genet.
Citation
Efthymiou, S., Leo, C.P., Deng, C., Lin, S.J., Maroofian, R., Lin, R., Karagoz, I., Zhang, K., Kaiyrzhanov, R., Scardamaglia, A., Owrang, D., Turchetti, V., Jahnke, F., Huang, K., Petree, C., Derrick, A.V., Rees, M.I., Alvi, J.R., Sultan, T., Li, C., Jacquemont, M.L., Tran-Mau-Them, F., Valenzuela-Palafoll, M., Sidlow, R., Yoon, G., Morrow, M.M., Carere, D.A., O'Connor, M., Fleischer, J., Gerkes, E.H., Phornphutkul, C., Isidor, B., Rivier-Ringenbach, C., Philippe, C., Kurul, S.H., Soydemir, D., Kara, B., Sunnetci-Akkoyunlu, D., Bothe, V., Platzer, K., Wieczorek, D., Koch-Hogrebe, M., Rahner, N., Thuresson, A.C., Matsson, H., Frykholm, C., Bozdoğan, S.T., Bisgin, A., Chatron, N., Lesca, G., Cabet, S., Tümer, Z., Hjortshøj, T.D., Rønde, G., Marquardt, T., Reunert, J., Afzal, E., Zamani, M., Azizimalamiri, R., Galehdari, H., Nourbakhsh, P., Chamanrou, N., Chung, S.K., Suri, M., Benke, P.J., Zaki, M.S., Gleeson, J.G., Calame, D.G., Pehlivan, D., Yilmaz, H.I., Gezdirici, A., Rad, A., Abumansour, I.S., Oprea, G., Bereketoğlu, M.B., Banneau, G., Julia, S., Zeighami, J., Ashoori, S., Shariati, G., Sedaghat, A., Sabri, A., Hamid, M., Parvas, S., Tajudin, T.A., Abdullah, U., Baig, S.M., Chung, W.K., Glazunova, O.O., Sabine, S., Cheema, H.A., Zifarelli, G., Bauer, P., Sidpra, J., Mankad, K., Vona, B., Fry, A.E., Varshney, G.K., Houlden, H., Fu, D. (2025) Biallelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder. American journal of human genetics. :.
Abstract
The post-transcriptional modification of tRNAs plays a crucial role in tRNA structure and function. Pathogenic variants in tRNA-modification enzymes have been implicated in a wide range of human neurodevelopmental and neurological disorders. However, the molecular basis for many of these disorders remains unknown. Here, we describe a comprehensive cohort of 43 individuals from 31 unrelated families with bi-allelic variants in tRNA methyltransferase 1 (TRMT1). These individuals present with a neurodevelopmental disorder universally characterized by developmental delay and intellectual disability, accompanied by variable behavioral abnormalities, epilepsy, and facial dysmorphism. The identified variants include ultra-rare TRMT1 variants, comprising missense and predicted loss-of-function variants, which segregate with the observed clinical pathology. Our findings reveal that several variants lead to mis-splicing and a consequent loss of TRMT1 protein accumulation. Moreover, cells derived from individuals harboring TRMT1 variants exhibit a deficiency in tRNA modifications catalyzed by TRMT1. Molecular analysis reveals distinct regions of TRMT1 required for tRNA-modification activity and binding. Notably, depletion of Trmt1 protein in zebrafish is sufficient to induce developmental and behavioral phenotypes along with gene-expression changes associated with disrupted cell cycle, immune response, and neurodegenerative disorders. Altogether, these findings demonstrate that loss of TRMT1-catalyzed tRNA modifications leads to intellectual disability and provides insight into the molecular underpinnings of tRNA-modification deficiency caused by pathogenic TRMT1 variants.
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Human Disease / Model
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Engineered Foreign Genes
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