Epigenetic Mosaicism in Genomic Imprinting Disorders
- 作者: Sazhenova E.A.1, Lebedev I.N.1
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隶属关系:
- Research Institute of Medical Genetics, Tomsk National Research Medical Center, Russian Academy of Sciences
- 期: 卷 55, 编号 10 (2019)
- 页面: 1196-1207
- 栏目: Reviews and Theoretical Articles
- URL: https://journals.rcsi.science/1022-7954/article/view/189589
- DOI: https://doi.org/10.1134/S1022795419100119
- ID: 189589
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详细
Differential gene expression during development is maintained by complex regulatory epigenetic mechanisms that provide the formation of different specialized cell types. Subsequently, a multicellular organism is a mosaic of cells with differing epigenetic characteristics. It seems likely that exceeding the limits of normal epigenetic variability may cause the occurrence of pathological mosaic states in which one part of the cell population has a normal epigenotype, while the other part carries modified epigenetic information. In this review, using the genomic imprinting as a classical epigenetic phenomenon, for the first time, the prevalence of epigenetic mosaicism and the mechanisms of its origin, as well as its role in the etiology of hereditary disorders, determined by the dysfunction of imprinted genomic loci are summarized.
作者简介
E. Sazhenova
Research Institute of Medical Genetics, Tomsk National Research Medical Center,Russian Academy of Sciences
编辑信件的主要联系方式.
Email: elena.sazhenova@medgenetics.ru
俄罗斯联邦, Tomsk, 634050
I. Lebedev
Research Institute of Medical Genetics, Tomsk National Research Medical Center,Russian Academy of Sciences
Email: elena.sazhenova@medgenetics.ru
俄罗斯联邦, Tomsk, 634050
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