Evidence map›Paper›PMID 39067069›Full record

ArticleGenetics2024

Poly(U) polymerase activity in Caenorhabditis elegans regulates abundance and tailing of sRNA and mRNA.

Leanne H Kelley, Ian V Caldas, Matthew T Sullenberger, Kevin E Yongblah, Adnan M Niazi, Anoop Iyer, Yini Li, Patrick Minty Tran, Eivind Valen, Yasir H Ahmed-Braimah and 1 more

Abstract read
In one paragraph

Article in Genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Leanne H KelleyDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Ian V CaldasDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Matthew T SullenbergerDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Kevin E YongblahDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Adnan M NiaziComputational Biology Unit, Department of Informatics, University of Bergen, 5008 Bergen, Norway.
Anoop IyerDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Yini LiDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Patrick Minty TranDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.
Eivind ValenComputational Biology Unit, Department of Informatics, University of Bergen, 5008 Bergen, Norway.
Yasir H Ahmed-BraimahDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.ORCID 0000-0002-5805-5894
Eleanor M MaineDepartment of Biology, Syracuse University, 107 College Place, Syracuse, NY 13244, USA.ORCID 0000-0002-6569-2701

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
The Genomic Basis and Molecular Mechanisms of SpeciationR35GM147454 · NIGMS · SYRACUSE UNIVERSITY · PI Yasir Ahmed-Braimah · 2022 to 2026
$2.0M
RNA uridylation as a protective mechanism in the germlineR15GM139096 · NIGMS · SYRACUSE UNIVERSITY · PI MAINE, ELEANOR M · 2020 to 2020
$450k
Identification of uridylated RNA important for germline maintenance in C. elegansR03HD091645 · NICHD · SYRACUSE UNIVERSITY · PI MAINE, ELEANOR M · 2018 to 2019
$150k
NICHD NIH HHS R03 HD091645NIGMS NIH HHS R15 GM139096NIGMS NIH HHS R35 GM147454NIH HHS P40 OD010440NIH HHS R03HD0091645Research Council of Norway #314216
6 · The paper itself

Abstract

Terminal nucleotidyltransferases add nucleotides to the 3' end of RNA to modify their stability and function. In Caenorhabditis elegans, the terminal uridyltransferases/poly(U) polymerases PUP-1 (aka CID-1, CDE-1), PUP-2, and PUP-3 affect germline identity, survival, and development. Here, we identify small RNA (sRNA) and mRNA targets of these PUPs and of a fourth predicted poly(U) polymerase, F43E2.1/PUP-4. Using genetic and RNA sequencing approaches, we identify RNA targets of each PUP and the U-tail frequency and length of those targets. At the whole organism level, PUP-1 is responsible for most sRNA U-tailing, and other PUPs contribute to modifying discrete subsets of sRNAs. Moreover, the expression of PUP-2, PUP-3, and especially PUP-4 limits uridylation on some sRNAs. The relationship between uridylation status and sRNA abundance suggests that U-tailing can have a negative or positive effect on abundance depending on context. sRNAs modified by PUP activity primarily target mRNAs that are ubiquitously expressed or most highly expressed in the germline. mRNA data obtained with a Nanopore-based method reveal that the addition of U-tails to nonadenylated mRNA is substantially reduced in the absence of PUP-3. Overall, this work identifies PUP RNA targets, defines the effect of uridylation loss on RNA abundance, and reveals the complexity of PUP regulation in C. elegans development.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsRNA, MessengerRNA NucleotidyltransferasesRNA, Small UntranslatedAnimalsCaenorhabditis elegans ProteinsRNA, MessengerRNA NucleotidyltransferasesRNA, Small Untranslated3′ tailingCaenorhabditis eleganspoly(U) polymerasesmall RNAuridylation

Identifiers

PMID39067069
PMCPMC11457939

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LicenceCC BY
Read underepoch 390

Registered trials

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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.