Abstract
ABSTRACTDuring tRNA maturation in yeast, aberrant pre-tRNAs are targeted for 3’-5’ degradation by the nuclear surveillance pathway, and mature tRNAs are targeted for 5’-3’ degradation by the rapid tRNA decay (RTD) pathway, due to lack of certain body modifications or to destabilizing mutations. Here we show that the RTD pathway also targets pre-tRNAs through an unknown, but distinct, mechanism that occurs after nuclear export. Anticodon stem RTD variants of both tRNATyr and tRNASer(CGA) are substrates for pre-tRNA RTD, triggered by the accumulation of end-matured unspliced pre-tRNA due to altered secondary structure of the region comprising the anticodon stem-loop and the intron. Furthermore, increased nuclear availability of a pre-tRNA RTD substrate can provoke decay by nuclear surveillance. We interpret these results in terms of a model of opportunistic tRNA decay, wherein tRNAs are degraded due to a combination of structural instability and increased availability to decay pathways.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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