A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
NXT2 is a key component of the RNA nuclear export factor complex in the human testis and essential for spermatogenesis
Tekijät: Dicke, Ann-Kristin; Ahmedani, Ammar; Ma, Lin; Herrmann, Leonie; van der Heijden, Godfried W.; Koser, Sophie A.; Krallmann, Claudia; Kalyon, Oguzhan; Xavier, Miguel J.; Veltman, Joris A.; Kliesch, Sabine; Neuhaus, Nina; Kotaja, Noora; Tuettelmann, Frank; Stallmeyer, Birgit
Kustantaja: NATURE PORTFOLIO
Kustannuspaikka: BERLIN
Julkaisuvuosi: 2025
Journal: Nature Communications
Tietokannassa oleva lehden nimi: NATURE COMMUNICATIONS
Lehden akronyymi: NAT COMMUN
Artikkelin numero: 6254
Vuosikerta: 16
Numero: 1
Sivujen määrä: 17
eISSN: 2041-1723
DOI: https://doi.org/10.1038/s41467-025-61463-0
Verkko-osoite: https://www.nature.com/articles/s41467-025-61463-0
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/499251529
In eukaryotes, the nucleocytoplasmic export of bulk poly(A)+-mRNAs through the nuclear pore complex is mediated by the ubiquitously expressed NXT1-NXF1 heterodimer. In humans, NXT1 has an X-chromosomal paralog, NXT2, which exhibits testis-enriched expression, suggesting a role in spermatogenesis. Here, we report the in vivo interaction of NXT2 with crucial components of the nuclear export machinery, including NXF1, the testis-specific NXF1 paralogs NXF2 and NXF3, and nuclear pore complex proteins. Binding to NXF2 and NXF3 is mediated by the NTF2-like domain of NXT2. By identifying infertile men with loss-of-function variants in NXT2 and NXF3, we link the impaired NXT2-NXF activity to disturbed germ cell development. The predominant absence of germ cells in men with NXT2 deficiency indicates its critical function already during fetal or first steps of germ cell development. In contrast, loss of NXF3 affects later stages of spermatogenesis, resulting in quantitatively and qualitatively impaired sperm production.
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Julkaisussa olevat rahoitustiedot:
The study was carried out within the frame of the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) funded Clinical Research Unit ‘Male Germ Cells’ (CRU326, project no. 329621271, grants to F.T. and N.N.). F.T. was supported by the Interdisciplinary Centre for Clinical Research Münster (IZKF, Tüt4/011/23). S.A.K. was supported by the Medical Faculty Münster’s ‘CareerS’ programme. N.K. was funded by the Novo Nordisk Foundation and the Jane and Aatos Erkko Foundation.
Open Access funding enabled and organized by Projekt DEAL.
