An ancestral tRNA maturation enzyme repurposed for cytoplasmic non-coding RNA processing
- 1Department of Biochemistry, School of Medicine, University of Patras, 26 504 Patras, Greece
Abstract
Ribonuclease Z enzymes remove 3' trailers from precursor tRNAs. In human cells, ELAC2/RNase ZL matures nuclear and mitochondrial pre-tRNAs, whereas the cytosolic short paralog ELAC1/RNase ZS repairs ANKZF1-cleaved tRNAs, but its broader substrate repertoire remains unclear. We investigated ELAC1 function using transcriptome profiling, small RNA sequencing, CLIP-seq, and biochemical reconstitution. ELAC1 was dispensable for canonical tRNA processing but associated with structured RNA polymerase III transcripts, prominently Y RNAs and vault RNAs (vtRNAs). Purified ELAC1 cleaved all four human vtRNAs near their 3' ends, with high-resolution mapping identifying a conserved cleavage position within the 3' extension. Efficient cleavage required structural features of the vtRNA terminal region. In contrast, ELAC2 showed little or no vtRNA cleavage under the conditions tested and displayed stricter substrate and cleavage-site selection on pre-tRNA. Loss and re-expression of ELAC1 altered structured ncRNA abundance and small-RNA end profiles. These findings identify vtRNAs as direct ELAC1 substrates and support functional specialization of human ELAC paralogs, with ELAC2 favoring precise pre-tRNA maturation and ELAC1 exhibiting broader RNA substrate specificity.
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BibTeX
@misc{shaukat2026ancestral,
title = {{An ancestral tRNA maturation enzyme repurposed for cytoplasmic non-coding RNA processing}},
author = {A.-N. Shaukat and M. F. Dondeti and A. Maniatis and I. Skeparnias and E. G. Kaliatsi and D. G. Anastasakis and J. Zhang and A. Vourekas and C. Stathopoulos},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.07.757187},
url = {https://www.biorxiv.org/content/10.64898/2026.10.07.757187v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - An ancestral tRNA maturation enzyme repurposed for cytoplasmic non-coding RNA processing
AU - A.-N. Shaukat
AU - M. F. Dondeti
AU - A. Maniatis
AU - I. Skeparnias
AU - E. G. Kaliatsi
AU - D. G. Anastasakis
AU - J. Zhang
AU - A. Vourekas
AU - C. Stathopoulos
PY - 2026
DA - 2026/10/07
PB - bioRxiv
DO - 10.64898/2026.10.07.757187
UR - https://www.biorxiv.org/content/10.64898/2026.10.07.757187v1
AB - Ribonuclease Z enzymes remove 3' trailers from precursor tRNAs. In human cells, ELAC2/RNase ZL matures nuclear and mitochondrial pre-tRNAs, whereas the cytosolic short paralog ELAC1/RNase ZS repairs ANKZF1-cleaved tRNAs, but its broader substrate repertoire remains unclear. We investigated ELAC1 function using transcriptome profiling, small RNA sequencing, CLIP-seq, and biochemical reconstitution. ELAC1 was dispensable for canonical tRNA processing but associated with structured RNA polymerase III transcripts, prominently Y RNAs and vault RNAs (vtRNAs). Purified ELAC1 cleaved all four human vtRNAs near their 3' ends, with high-resolution mapping identifying a conserved cleavage position within the 3' extension. Efficient cleavage required structural features of the vtRNA terminal region. In contrast, ELAC2 showed little or no vtRNA cleavage under the conditions tested and displayed stricter substrate and cleavage-site selection on pre-tRNA. Loss and re-expression of ELAC1 altered structured ncRNA abundance and small-RNA end profiles. These findings identify vtRNAs as direct ELAC1 substrates and support functional specialization of human ELAC paralogs, with ELAC2 favoring precise pre-tRNA maturation and ELAC1 exhibiting broader RNA substrate specificity.
ER -