Evidence map›Paper›PMID 40680550›Full record

ArticleReproductive biomedicine online2025

TKTL1: a new candidate gene in non-obstructive azoospermia.

Agnieszka Malcher, Mikołaj Smolibowski, Tomasz Stokowy, Hermann Bauer, Alicja Patyk, Piotr Jedrzejczak, Jagoda Kostyk, Zuzanna Graczyk, Rim Ibrahim, Katarzyna Bednarek-Rajewska and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Reproductive biomedicine online, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Agnieszka MalcherInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland. Electronic address: agnieszka.malcher@igcz.poznan.pl.
Mikołaj SmolibowskiInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Tomasz StokowyIT Division, University of Bergen, Bergen, Norway.
Hermann BauerDepartment of Developmental Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Alicja PatykInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Piotr JedrzejczakCenter of Obstetrics, Gynecology and Infertility Treatment - Pastelova Clinic, Poznan, Poland; Department of Cell Biology, Poznan University of Medical Sciences, Poznan, Poland.
Jagoda KostykInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Zuzanna GraczykInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Rim IbrahimInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland.
Katarzyna Bednarek-RajewskaDepartment of Clinical Pathology, Poznan University of Medical Sciences, Poznan, Poland.
Anna BergerCenter of Obstetrics, Gynecology and Infertility Treatment - Pastelova Clinic, Poznan, Poland.
Alexander N YatsenkoDepartment of Obstetrics and Gynecology and Reproductive Sciences, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Maciej KurpiszInstitute of Human Genetics, Polish Academy of Sciences, Poznan, Poland. Electronic address: maciej.kurpisz@igcz.poznan.pl.

Funding

Project IIIP50HD096723 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI John C Schimenti · 2019 to 2026
$15.0M
Genomic signatures of X-linked and autosomal candidate-genes in azoospermiaR21HD080755 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI YATSENKO, ALEXANDER N · 2015 to 2016
$448k
NICHD NIH HHS P50 HD096723NICHD NIH HHS R21 HD080755
6 · The paper itself

Abstract

research questionWhat role does TKTL1 gene serve in human spermatogenesis and does its mutation trigger non-obstructive azoospermia (NOA)?

designThe genetic background of NOA remains poorly explored. Recent studies using next generation sequencing techniques, however, have uncovered some NOA causative genes, including the TKTL1 gene. The aim of this study was to define the function of the TKTL1 gene in human spermatogenesis by inducing its overexpression in human testicular primary (hTP) cells, and verifying these results in male gonad tissue samples collected from patients with NOA determining the genes cluster regulated by TKTL1.

resultsSuccessful overexpression of the TKTL1 gene was achieved in hTP cells; the TKTL1 gene expression was significantly higher in genetically modified cells compared with both controls applied. RNA-sequencing was used to select 20 genes in which expression significantly differed in the modified hTP cells overexpressing TKTL1 gene compared with controls. Male gonad tissue samples collected from patients with NOA harbouring a mutation in the TKTL1 gene showed a significant downregulation in HERC5, CSF3, HES1 and HSPA1B genes, compared with patients with azoospermia without mutation in the TKTL1 gene (negative control) as well as control samples with normal spermatogenesis. This was in accordance with results obtained with hTP cells, as the overexpression of the TKTL1 gene correlated with an increased expression level of the mentioned genes compared with controls.

conclusionsThe TKTL1 gene is likely involved in the regulation of gametogenesis affecting the proliferation and differentiation of germ cells at the early stage of spermatogenesis.

Indexed as

AzoospermiaSpermatogenesisTransketolaseAdolescentAdultCell DifferentiationCell ProliferationHumansMaleMiddle AgedMutationPrimary Cell CultureSpermatozoaTestisYoung AdultTKTL1 protein, humanTransketolaseazoospermiabiomarkersmale infertilityNOATKTL1 gene

Identifiers

PMID40680550
PMCPMC12448108

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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.