Evidence map›Paper›PMID 41680579›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2026

Molecular Characterization of the Murine Catsper4 Promoter and its Regulation by CREMτ.

Sergio Federico López-Guzmán, Diego Eduardo Sánchez-Jasso, Javier Hernández-Sánchez, Norma Oviedo, Rosa Maria Bermudez-Cruz

Abstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2026. 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.

Sergio Federico López-GuzmánCentro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Departamento de Genética y Biología Molecular, Ciudad de México, 07360, México.ORCID 0000-0002-4381-4931
Diego Eduardo Sánchez-JassoCentro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Departamento de Genética y Biología Molecular, Ciudad de México, 07360, México.ORCID 0009-0001-1229-4232
Javier Hernández-SánchezCentro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Departamento de Genética y Biología Molecular, Ciudad de México, 07360, México.ORCID 0000-0001-5773-6877
Norma OviedoInstituto Mexicano del Seguro Social, Unidad de Investigación Médica en Inmunología e Infectología, Centro Médico Nacional, La Raza, Ciudad de México, 02990, México. naoviedoa@yahoo.com.mx.ORCID 0000-0002-2359-5751
Rosa Maria Bermudez-CruzCentro de Investigación y Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV), Departamento de Genética y Biología Molecular, Ciudad de México, 07360, México. roberm@cinvestav.mx.ORCID 0000-0003-0463-9357

Funding

Instituto Mexicano del Seguro Social IMSS R-2023-785-056
6 · The paper itself

Abstract

Cation channel sperm-associated protein 4 (CATSPER4) is a subunit of the sperm-specific cation/calcium channel, CatSper, located in the principal piece of the sperm flagellum. It is expressed during the late stages of spermatogenesis, and disruption of the gene encoding this protein leads to male infertility. Mutations in Catsper4 are linked to asthenozoospermia. However, the molecular mechanisms regulating Catsper4 expression remain unclear. Here, we present a detailed molecular characterization of the Catsper4 promoter in mice, focusing on the role of the cAMP-responsive element modulator isoform τ (CREMτ) in its transcriptional regulation. Analysis of publicly available metagenomic chromatin immunoprecipitation-sequencing (ChIP-seq) data revealed the presence of activation histone marks-H3K4me3, H3K4me1, and H3K27ac-within a region corresponding to the 631 bp predicted promoter, suggesting an active promoter region. Although the predicted Catsper4 promoter showed minimal activity, a 65 bp deletion at the 3'-end of the promoter significantly enhanced the transcription. Moreover, removal of the 239 bp in the 5'-flanking region also increased the transcriptional activity, indicating that the core promoter region spans the region from - 99 to + 63 bp relative to the transcription start site (TSS). Notably, a cAMP-responsive element was predicted at + 91, a relevant site in the regulation of other Catsper family genes. To explore its function, we mutated this site and overexpressed CREMτ. Electrophoretic mobility shift assays (EMSA) and ChIP assays confirmed that CREMτ binds to the murine Catsper4 promoter both in vitro and in vivo. This study provides the first functional analysis of the Catsper4 promoter, shedding light on the mechanisms regulating its expression and highlighting the key role of CREMτ in this process.

Indexed as

Calcium ChannelsCyclic AMP Response Element ModulatorPromoter Regions, GeneticAnimalsGene Expression RegulationMaleMiceSperm ProteinsCalcium ChannelsCrem protein, mouseCyclic AMP Response Element ModulatorSperm ProteinsCatsper4Core promoterCREMτSpermatogenesisTranscriptional regulation

Identifiers

PMID41680579
PMCPMC12992399

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.