Pseudouridinylation of mRNA coding sequences alters translation.

Abstract:

:Chemical modifications of RNAs have long been established as key modulators of nonprotein-coding RNA structure and function in cells. There is a growing appreciation that messenger RNA (mRNA) sequences responsible for directing protein synthesis can also be posttranscriptionally modified. The enzymatic incorporation of mRNA modifications has many potential outcomes, including changing mRNA stability, protein recruitment, and translation. We tested how one of the most common modifications present in mRNA coding regions, pseudouridine (Ψ), impacts protein synthesis using a fully reconstituted bacterial translation system and human cells. Our work reveals that replacing a single uridine nucleotide with Ψ in an mRNA codon impedes amino acid addition and EF-Tu GTPase activation. A crystal structure of the Thermus thermophilus 70S ribosome with a tRNAPhe bound to a ΨUU codon in the A site supports these findings. We also find that the presence of Ψ can promote the low-level synthesis of multiple peptide products from a single mRNA sequence in the reconstituted translation system as well as human cells, and increases the rate of near-cognate Val-tRNAVal reacting on a ΨUU codon. The vast majority of Ψ moieties in mRNAs are found in coding regions, and our study suggests that one consequence of the ribosome encountering Ψ can be to modestly alter both translation speed and mRNA decoding.

authors

Eyler DE,Franco MK,Batool Z,Wu MZ,Dubuke ML,Dobosz-Bartoszek M,Jones JD,Polikanov YS,Roy B,Koutmou KS

doi

10.1073/pnas.1821754116

subject

Has Abstract

pub_date

2019-11-12 00:00:00

pages

23068-23074

issue

46

eissn

0027-8424

issn

1091-6490

pii

1821754116

journal_volume

116

pub_type

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