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De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Purpose - Polycomb group proteins are key epigenetic transcriptional regulators. Multiple neurodevelopmental disorders are associated with pathogenic variants of the genes encoding Polycomb group proteins. RYBP is a core component of the noncanonical Polycomb Repressor Complex 1; however, its role i...

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Hauptverfasser: Weisz-Hubshman, Monika (VerfasserIn) , Burrage, Lindsay C. (VerfasserIn) , Jangam, Sharayu V. (VerfasserIn) , Rosenfeld, Jill A. (VerfasserIn) , Hardenberg, Sandra von (VerfasserIn) , Bergmann, Anke (VerfasserIn) , Richter, Manuela Friederike (VerfasserIn) , Rydzanicz, Malgorzata (VerfasserIn) , Ploski, Rafal (VerfasserIn) , Stembalska, Agnieszka (VerfasserIn) , Chung, Wendy K. (VerfasserIn) , Hernan, Rebecca R. (VerfasserIn) , Lim, Foong Y. (VerfasserIn) , Brunet, Theresa (VerfasserIn) , Syrbe, Steffen (VerfasserIn) , Keren, Boris (VerfasserIn) , Heide, Solveig (VerfasserIn) , Murdock, David R. (VerfasserIn) , Dai, Hongzheng (VerfasserIn) , Xia, Fan (VerfasserIn) , Ketkar, Shamika (VerfasserIn) , Dawson, Brian (VerfasserIn) , Narayanan, Vinodh (VerfasserIn) , Graves, Hillary K. (VerfasserIn) , Wangler, Michael F. (VerfasserIn) , Bacino, Carlos (VerfasserIn) , Lee, Brendan (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: April 2025
In: Genetics in medicine
Year: 2025, Jahrgang: 27, Heft: 4, Pages: 1-17
ISSN:1530-0366
DOI:10.1016/j.gim.2025.101369
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.gim.2025.101369
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S1098360025000164
Volltext
Verfasserangaben:Monika Weisz-Hubshman, Lindsay C. Burrage, Sharayu V. Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke Bergmann, Manuela Friederike Richter, Malgorzata Rydzanicz, Rafal Ploski, Agnieszka Stembalska, Wendy K. Chung, Rebecca R. Hernan, Foong Y. Lim, Theresa Brunet,Steffen Syrbe, Boris Keren, Solveig Heide, David R. Murdock, Hongzheng Dai, Fan Xia, Shamika Ketkar, Brian Dawson, Vinodh Narayanan, Hillary K. Graves, Undiagnosed Diseases Network, Michael F. Wangler, Carlos Bacino, Brendan Lee
Beschreibung
Zusammenfassung:Purpose - Polycomb group proteins are key epigenetic transcriptional regulators. Multiple neurodevelopmental disorders are associated with pathogenic variants of the genes encoding Polycomb group proteins. RYBP is a core component of the noncanonical Polycomb Repressor Complex 1; however, its role in disease is unclear. - Methods - Functional consequences of RYBP variants were assessed using in vitro cellular and in vivo Drosophila melanogaster studies. - Results - We described 7 individuals with heterozygous de novo variants of RYBP and their clinical findings, including severe developmental delay, dysmorphisms, and multiple congenital anomalies. We showed that all single-nucleotide variants in RYBP localize to the N-terminal domain of the gene, which encodes the zinc-finger domain and ubiquitin-binding moiety. In vitro studies have demonstrated that the RYBP c.132C>G p.(Cys44Trp) variant causes reduced protein expression but does not affect the binding of YY1, RING1B, or ubiquitin. In vivo overexpression studies in Drosophila melanogaster showed a dramatic functional difference between human RYBP and its variant forms, affecting the C44 amino acid residue. DNA methylation studies suggested a possible episignature associated with RYBP-related disorder. - Conclusion - Heterozygous de novo variants in RYBP are associated with an identifiable syndromic neurodevelopmental disorder with multiple congenital anomalies.
Beschreibung:Online verfügbar: 28. Januar 2025, Artikelversion: 04. März 2025
Gesehen am 08.09.2025
Beschreibung:Online Resource
ISSN:1530-0366
DOI:10.1016/j.gim.2025.101369

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