The vault RNA of Trypanosoma brucei plays a role in the production of trans-spliced mRNA

Nikolay G. Kolev, K. Shanmugha Rajan, Kazimierz T. Tycowski, Justin Y. Toh, Huafang Shi, Yuling Lei, Shulamit Michaeli, Christian Tschudi

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

The vault ribonucleoprotein (RNP), comprising vault RNA (vtRNA) and telomerase-associated protein 1 (TEP1), is found in many eukaryotes. However, previous studies of vtRNAs, for example in mammalian cells, have failed to reach a definitive conclusion about their function. vtRNAs are related to Y RNAs, which are complexed with Ro protein and influence Ro's function in noncoding RNA (ncRNA) quality control and processing. In Trypanosoma brucei, the small noncoding TBsRNA-10 was first described in a survey of the ncRNA repertoire in this organism. Here, we report that TBsRNA-10 in T. brucei is a vtRNA, based on its association with TEP1 and sequence similarity to those of other known and predicted vtRNAs.Weobserved that like vtRNAs in other species, TBsRNA-10 is transcribed by RNA polymerase III, which in trypanosomes also generates the spliceosomal U-rich small nuclear RNAs. In T. brucei, spliced leader (SL)- mediated trans-splicing of pre-mRNAs is an obligatory step in gene expression, and we found here that T. brucei's vtRNA is highly enriched in a non-nucleolar locus in the cell nucleus implicated in SL RNP biogenesis. Using a newly developed permeabilized cell system for the bloodstream form of T. brucei, we show that down-regulated vtRNA levels impair transspliced mRNA production, consistent with a role of vtRNA in trypanosome mRNA metabolism. Our results suggest a common theme for the functions of vtRNAs and Y RNAs. We conclude that by complexing with their protein-binding partners TEP1 and Ro, respectively, these two RNA species modulate the metabolism of various RNA classes.

Original languageEnglish
Pages (from-to)15559-15574
Number of pages16
JournalJournal of Biological Chemistry
Volume294
Issue number43
DOIs
StatePublished - 25 Oct 2019

Bibliographical note

Publisher Copyright:
© 2019 Kolev et al.

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