tRNA cleavage: a new insight

S Rashad, K Niizuma, T Tominaga - Neural regeneration …, 2020 - journals.lww.com
Over the past decades, tRNA was found to be a rich hub of RNA modifications such as 1-
methyladenosine and 5-methycytosine modifications and others, holding more than half of …

Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease

K Asano, T Suzuki, A Saito, FY Wei… - Nucleic acids …, 2018 - academic.oup.com
Modified uridine containing taurine, 5-taurinomethyluridine (τm5U), is found at the anticodon
first position of mitochondrial (mt-) transfer RNAs (tRNAs). Previously, we reported that τm5U …

Queuosine tRNA Modification: Connecting the Microbiome to the Translatome

S Rashad - Bioessays, 2025 - Wiley Online Library
Transfer RNA (tRNA) modifications play an important role in regulating mRNA translation at
the codon level. tRNA modifications can influence codon selection and optimality, thus …

A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function

M Zhou, L Xue, Y Chen, H Li, Q He, B Wang… - Journal of Biological …, 2018 - ASBMB
Defective nucleotide modifications of mitochondrial tRNAs have been associated with
several human diseases, but their pathophysiology remains poorly understood. In this …

A deafness-and diabetes-associated tRNA mutation causes deficient pseudouridinylation at position 55 in tRNAGlu and mitochondrial dysfunction

M Wang, H Liu, J Zheng, B Chen, M Zhou… - Journal of Biological …, 2016 - ASBMB
Several mitochondrial tRNA mutations have been associated with maternally inherited
diabetes and deafness. However, the pathophysiology of these tRNA mutations remains …

Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism

D Chen, Z Zhang, C Chen, S Yao, Q Yang… - Nucleic acids …, 2019 - academic.oup.com
GTPBP3 is a highly conserved tRNA modifying enzyme for the biosynthesis of τm5U at the
wobble position of mitochondrial tRNAGlu, tRNAGln, tRNALys, tRNATrp and tRNALeu …

Mammalian and invertebrate models as complementary tools for gaining mechanistic insight on muscle responses to spaceflight

T Cahill, H Cope, JJ Bass, EG Overbey… - International Journal of …, 2021 - mdpi.com
Bioinformatics approaches have proven useful in understanding biological responses to
spaceflight. Spaceflight experiments remain resource intensive and rare. One outstanding …

Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension

L Xue, M Wang, H Li, H Wang, F Jiang, L Hou, J Geng… - Mitochondrion, 2016 - Elsevier
Background Mitochondria have the profound impact on vascular function in both health and
disease. However, mitochondrial genetic determinants for the development of hypertension …

[HTML][HTML] Mitochondrial tRNA mutations in 887 Chinese subjects with hearing loss

J Zheng, X Bai, Y Xiao, Y Ji, F Meng, M Aishanjiang… - Mitochondrion, 2020 - Elsevier
Mutations in the mitochondrial tRNAs have been reported to be the important cause of
hearing loss. However, only a few cases have been identified thus far and the prevalence of …

A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function

M Wang, Y Peng, J Zheng, B Zheng, X Jin… - Nucleic acids …, 2016 - academic.oup.com
In this report, we investigated the pathogenic mechanism underlying the deafness-
associated mitochondrial (mt) tRNAAsp 7551A> G mutation. The m. 7551A> G mutation is …