Evidence map›Paper›PMID 39995041›Full record

ArticleNucleic acids research2025

The lncRNA DUBR is regulated by CTCF and coordinates chromatin landscape and gene expression in hematopoietic cells.

Hober Nelson Núñez-Martínez, Gustavo Tapia-Urzúa, Ángel Josué Cerecedo-Castillo, Carlos Alberto Peralta-Alvarez, Georgina Guerrero, Maite Huarte, Félix Recillas-Targa

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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

7 authors.

Hober Nelson Núñez-MartínezInstituto de Fisiología Celular, Departamento de Genética Molecular, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.ORCID 0000-0003-1726-2499
Gustavo Tapia-UrzúaInstituto de Fisiología Celular, Departamento de Genética Molecular, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.ORCID 0009-0005-9246-7445
Ángel Josué Cerecedo-CastilloInstituto de Fisiología Celular, Departamento de Genética Molecular, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.ORCID 0009-0005-0263-5215
Carlos Alberto Peralta-AlvarezInstituto de Fisiología Celular, Departamento de Genética Molecular, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.ORCID 0000-0001-6103-5133
Georgina GuerreroInstituto de Fisiología Celular, Departamento de Genética Molecular, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.ORCID 0000-0003-2933-1498
Maite HuarteCenter for Applied Medical Research, Department of Gene Therapy and Regulation of Gene Expression, University of Navarra, Pamplona, 31008, Spain.ORCID 0000-0003-3753-6493
Félix Recillas-TargaInstituto de Fisiología Celular, Departamento de Genética Molecular, Universidad Nacional Autónoma de México, 04510, Ciudad de México, México.ORCID 0000-0002-4336-0407

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías A1-S-11844European Research Council Consolidator 771425;Fondo Europeo de Desarrollo Regional/Ministerio de Ciencia, Innovación y Universidades-Agencia Estatal de Investigación BFU2017-82773-PFundación Miguel Alemán A.C.Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica DGAPA-PAPIIT IN203620Universidad Nacional Autónoma de México
6 · The paper itself

Abstract

Master hematopoietic transcription factors (TFs) and long noncoding RNAs (lncRNAs) coordinate shaping lineage-specific gene expression programs during hematopoietic differentiation. The architectural protein CCCTC-binding factor (CTCF) has emerged as a pivotal regulator of gene expression in cell differentiation. However, the relationship and its regulatory effect of CTCF on lncRNA genes in hematopoiesis remain elusive. We demonstrated that CTCF constrains the lncRNA DUBRtranscription throughout erythroid differentiation. DUBR is highly expressed in human hematopoietic stem and progenitor cells (HSPCs) but depleted in erythroblasts. DUBR perturbation dysregulates hematopoietic-erythroid cell differentiation genes and facilitates genome-wide activation of regulatory elements. A genomic map of RNA occupancy revealed that DUBR associates with a set of genes involved in regulating hematopoietic differentiation, including the erythroid repressor HES1, which targets a subset of regulatory elements of DUBR-dysregulated genes. Our results support the role of DUBR as a regulator of a hematopoietic differentiation gene program by coordinating the expression of genes and influencing their chromatin regulatory landscape.

Indexed as

CCCTC-Binding FactorChromatinGene Expression RegulationHematopoiesisHematopoietic Stem CellsRNA, Long NoncodingCell DifferentiationHumansCCCTC-Binding FactorChromatinCTCF protein, humanRNA, Long Noncoding

Identifiers

PMID39995041
PMCPMC11850227

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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 Socratic graph.