Evidence map›Paper›PMID 40956881›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

SUMO conjugation to promoter-proximal sequence elements-associated proteins impacts on snRNA transcription.

Laureano Bragado, Berta Pozzi, Inés Beckerman, Melina Magalnik, Anabella Srebrow

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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

5 authors.

Laureano BragadoUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires C1428EGA, Argentina.
Berta PozziUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires C1428EGA, Argentina.
Inés BeckermanUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires C1428EGA, Argentina.ORCID 0000-0002-6362-1459
Melina MagalnikUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires C1428EGA, Argentina.
Anabella SrebrowUniversidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires C1428EGA, Argentina.ORCID 0000-0002-1468-4736

Funding

Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación (agenciaidiar) 2017-0111Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación (agenciaidiar) 2019-00263Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación (agenciaidiar) 2020-00198H2020-Marie Sklodowska-Curie Research and Innovation Staff Exchange Program LYSOMODMinisterio de Ciencia, Tecnología e Innovación (MINCyT) Red Federal de Alto Impacto- CONVE-2023-100766162-APN-MCTUBA | Secretaría de Ciencia y Técnica, Universidad de Buenos Aires (UBACyT) 20020170100045BAUBA | Secretaría de Ciencia y Técnica, Universidad de Buenos Aires (UBACyT) 20020220200041BA
6 · The paper itself

Abstract

The noncoding small nuclear RNAs (snRNAs) associate with a large set of proteins to form small nuclear ribonucleoprotein particles (snRNPs). While the function of snRNAs is well characterized, the regulation of their transcription remains poorly understood. Recently, we demonstrated that SUMO conjugation regulates snRNA3' end processing. To further study the connection between SUMOylation and snRNA biogenesis, we generated a CRISPR/dCas9 tool comprising a catalytically inactive Cas9 (dCas9) fused to the catalytic domain of the SUMO protease SENP1 (dCas9-SENP1). Here, we show that snRNA transcription decreases when dCas9-SENP1 is delivered to their promoter-proximal sequence elements (PSE), indicating that SUMO conjugation to proteins associated with snRNA promoters is necessary for proper transcriptional activity. Focusing on SNAPC1, a subunit of the snRNA-specific transcription complex SNAPc, we identified lysine residues 245 and 333 as SUMO acceptor sites and generated a SUMOylation-deficient mutant of this protein (SNAPC1 2KR). To explore the relevance of SNAPC1 SUMOylation on snRNA transcription, we generated a cell line carrying an inducible degron system for depletion of the endogenous SNAPC1 protein. This system led us to demonstrate that SNAPC1 2KR is unable to sustain basal levels of snRNA transcription. By tagging endogenous SNAPC3 and SNAPC4, two other subunits of SNAPc, we show that while SNAPC1 SUMOylation-deficient mutant is able to interact with SNAPC3, its interaction with SNAPC4 is affected, despite the fact it is still recruited to the PSE. Altogether, these results indicate that SNAPC1 SUMOylation is required for proper snRNA transcription and SNAPc complex assembly.

Indexed as

Promoter Regions, GeneticRNA, Small NuclearTranscription, GeneticCysteine EndopeptidasesHEK293 CellsHeLa CellsHumansSumoylationCysteine EndopeptidasesRNA, Small NuclearSENP1 protein, humanCRISPRposttranslational modificationSNAPcSUMO proteases

Identifiers

PMID40956881
PMCPMC12478075

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.