Evidence map›Paper›PMID 38194449›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Sm complex assembly and 5' cap trimethylation promote selective processing of snRNAs by the 3' exonuclease TOE1.

Tiantai Ma, Erica S Xiong, Rea M Lardelli, Jens Lykke-Andersen

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Tiantai MaDepartment of Molecular Biology, School of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.ORCID 0000-0002-7150-7808
Erica S XiongDepartment of Molecular Biology, School of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.ORCID 0009-0000-8023-5720
Rea M LardelliDepartment of Molecular Biology, School of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
Jens Lykke-AndersenDepartment of Molecular Biology, School of Biological Sciences, University of California, San Diego, La Jolla, CA 92093.
University of California San Diego · US

Funding

UCSD/SDSU IRACDAK12GM068524 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TREJO, JOANN · 2003 to 2025
$24.4M
Mechanisms of human RNA turnover and quality controlR35GM118069 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LYKKE-ANDERSEN, JENS · 2016 to 2025
$5.1M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
What is the molecular function of MOV10 ATPase in RNA-induced silencing of mRNA?F32GM106706 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LARDELLI, REA M · 2013 to 2014
$107k
NIGMS NIH HHS F32 GM106706NIGMS NIH HHS K12 GM068524NIGMS NIH HHS R35 GM118069NIH HHS S10 OD026929
6 · The paper itself

Abstract

Competing exonucleases that promote 3' end maturation or degradation direct quality control of small non-coding RNAs, but how these enzymes distinguish normal from aberrant RNAs is poorly understood. The Pontocerebellar Hypoplasia 7 (PCH7)-associated 3' exonuclease TOE1 promotes maturation of canonical small nuclear RNAs (snRNAs). Here, we demonstrate that TOE1 achieves specificity toward canonical snRNAs through their Sm complex assembly and cap trimethylation, two features that distinguish snRNAs undergoing correct biogenesis from other small non-coding RNAs. Indeed, disruption of Sm complex assembly via snRNA mutations or protein depletions obstructs snRNA processing by TOE1, and in vitro snRNA processing by TOE1 is stimulated by a trimethylated cap. An unstable snRNA variant that normally fails to undergo maturation becomes fully processed by TOE1 when its degenerate Sm binding motif is converted into a canonical one. Our findings uncover the molecular basis for how TOE1 distinguishes snRNAs from other small non-coding RNAs and explain how TOE1 promotes maturation specifically of canonical snRNAs undergoing proper processing.

Indexed as

ExonucleasesRNA, Small NuclearMutationQuality ControlRNAExonucleasesRNARNA, Small Nuclear3′ end processing5′ cap trimethylationSm complexsnRNATOE1

Identifiers

PMID38194449
PMCPMC10801842
OpenAlexW4390743542

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.