Evidence map›Paper›PMID 40884004›Full record

ReviewFEBS letters2025

A working model for cytoplasmic assembly of H/ACA snoRNPs.

Alberto Angrisani, Maria Furia

Abstract readReview
In one paragraph

Review in FEBS letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Alberto AngrisaniDepartment of Biology, University of Naples "Federico II", Complesso Universitario Monte Santangelo, Italy.ORCID https://orcid.org/0000-0001-7881-1290
Maria FuriaDepartment of Biology, University of Naples "Federico II", Complesso Universitario Monte Santangelo, Italy.ORCID https://orcid.org/0000-0002-9603-7689

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudouridylation occurs on all types of cellular RNAs. As a catalytic component of nuclear H/ACA ribonucleoproteins (RNPs), the pseudouridine synthase dyskerin exerts a general impact on multiple fundamental cellular processes. Although this protein has been investigated in detail, its cytoplasmic roles have been largely overlooked, despite the identification of a minor splice variant showing a prevalent cytoplasmic localization. In this perspective, we discuss the role of this minor isoform in the composition, assembly, and function of H/ACA RNPs. On this basis, we propose a model in which cytoplasmic regulation modulates the integration of distinct dyskerin isoforms within preassembly complexes, consequently also influencing their nuclear import. This mechanism could govern pseudouridylation, cellular growth, and mRNA translation. Impact statement Human Dyskerin is the pseudouridine-synthase component of H/ACA RNPs. Two isoforms have been characterized: the abundant Iso1, mainly nuclear, and Iso3, mainly cytoplasmic but occasionally imported into nuclei. We propose a model accounting for a regulated participation of both isoforms in the cytoplasmic pre-assembly of H/ACA RNPs.

Indexed as

Cell Cycle ProteinsCytoplasmNuclear ProteinsRibonucleoproteins, Small NucleolarAnimalsCell NucleusHumansProtein IsoformsCell Cycle ProteinsDKC1 protein, humanNuclear ProteinsProtein IsoformsRibonucleoproteins, Small NucleolardyskeratosisdyskerinpseudouridylationribosomopathiessnoRNPs biogenesistranslational regulation

Identifiers

PMID40884004
PMCPMC12683209

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.