Evidence map›Paper›PMID 37065848›Full record

ArticleFrontiers in cell and developmental biology2023

Spermiogenesis alterations in the absence of CTCF revealed by single cell RNA sequencing.

Ulises Torres-Flores, Fernanda Díaz-Espinosa, Tayde López-Santaella, Rosa Rebollar-Vega, Aarón Vázquez-Jiménez, Ian J Taylor, Rosario Ortiz-Hernández, Olga M Echeverría, Gerardo H Vázquez-Nin, María Concepción Gutierrez-Ruiz and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 6 institutions in 2 countries.

Ulises Torres-FloresGraduate Program in Experimental Biology, DCBS, Universidad Autónoma Metropolitana, Unidad Iztapalapa, México City, Mexico.
Fernanda Díaz-EspinosaBiología de Células Individuales (BIOCELIN), Laboratorio de Investigación en Patología Experimental, Hospital Infantíl de México Federico Gómez, México City, Mexico.
Tayde López-SantaellaBiología de Células Individuales (BIOCELIN), Laboratorio de Investigación en Patología Experimental, Hospital Infantíl de México Federico Gómez, México City, Mexico.
Rosa Rebollar-VegaCoordinación de la Investigación Científica-Red de Apoyo a la Investigación, Universidad Nacional Autónoma de México e Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City, Mexico.
Aarón Vázquez-JiménezCoordinación de la Investigación Científica-Red de Apoyo a la Investigación-Centro de Ciencias de la Complejidad, Universidad Nacional Autónoma de México, México City, Mexico.
Ian J TaylorBD Life Sciences Informatics, Ashland, OR, United States.
Rosario Ortiz-HernándezLaboratorio de Microscopía Electrónica, Facultad de Ciencias, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Olga M EcheverríaLaboratorio de Microscopía Electrónica, Facultad de Ciencias, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Gerardo H Vázquez-NinLaboratorio de Microscopía Electrónica, Facultad de Ciencias, Universidad Nacional Autónoma de México, Mexico City, Mexico.
María Concepción Gutierrez-RuizLaboratorio de Fisiología Celular y Medicina Traslacional, Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana-I, Mexico City, Mexico.
Inti Alberto De la Rosa-VelázquezCoordinación de la Investigación Científica-Red de Apoyo a la Investigación, Universidad Nacional Autónoma de México e Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, México City, Mexico.
Osbaldo Resendis-AntonioCoordinación de la Investigación Científica-Red de Apoyo a la Investigación-Centro de Ciencias de la Complejidad, Universidad Nacional Autónoma de México, México City, Mexico.
Abrahan Hernández-HernandezBiología de Células Individuales (BIOCELIN), Laboratorio de Investigación en Patología Experimental, Hospital Infantíl de México Federico Gómez, México City, Mexico.
Hospital Infantil de México Federico Gómez · MXUniversidad Nacional Autónoma de México · MXInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXNational Institute of Genomic Medicine · MXUniversidad Autónoma Metropolitana · MXAshland (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CTCF is an architectonic protein that organizes the genome inside the nucleus in almost all eukaryotic cells. There is evidence that CTCF plays a critical role during spermatogenesis as its depletion produces abnormal sperm and infertility. However, defects produced by its depletion throughout spermatogenesis have not been fully characterized. In this work, we performed single cell RNA sequencing in spermatogenic cells with and without CTCF. We uncovered defects in transcriptional programs that explain the severity of the damage in the produced sperm. In the early stages of spermatogenesis, transcriptional alterations are mild. As germ cells go through the specialization stage or spermiogenesis, transcriptional profiles become more altered. We found morphology defects in spermatids that support the alterations in their transcriptional profiles. Altogether, our study sheds light on the contribution of CTCF to the phenotype of male gametes and provides a fundamental description of its role at different stages of spermiogenesis.

Indexed as

CTCFmouse testisScRNA-seqspermspermatogenesis

Identifiers

PMID37065848
PMCPMC10097911
OpenAlexW4361281786

What OpenQuestion holds

Textmetadata
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.