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Dosage Compensation in Females with X-Linked Metabolic Disorders

Through the use of new genomic and metabolomic technologies, our comprehension of the molecular and biochemical etiologies of genetic disorders is rapidly expanding, and so are insights into their varying phenotypes. Dosage compensation (lyonization) is an epigenetic mechanism that balances the expr...

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Detalles Bibliográficos
Autores principales: Juchniewicz, Patrycja, Piotrowska, Ewa, Kloska, Anna, Podlacha, Magdalena, Mantej, Jagoda, Węgrzyn, Grzegorz, Tukaj, Stefan, Jakóbkiewicz-Banecka, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123450/
https://www.ncbi.nlm.nih.gov/pubmed/33925963
http://dx.doi.org/10.3390/ijms22094514
Descripción
Sumario:Through the use of new genomic and metabolomic technologies, our comprehension of the molecular and biochemical etiologies of genetic disorders is rapidly expanding, and so are insights into their varying phenotypes. Dosage compensation (lyonization) is an epigenetic mechanism that balances the expression of genes on heteromorphic sex chromosomes. Many studies in the literature have suggested a profound influence of this phenomenon on the manifestation of X-linked disorders in females. In this review, we summarize the clinical and genetic findings in female heterozygotic carriers of a pathogenic variant in one of ten selected X-linked genes whose defects result in metabolic disorders.