SAMMY-SEQ REVEALS EARLY ALTERATION OF HETEROCHROMATIN AND DEREGULATION OF BIVALENT GENES IN HUTCHINSON-GILFORD PROGERIA SYNDROME

SAMMY-seq reveals early alteration of heterochromatin and deregulation of bivalent genes in Hutchinson-Gilford Progeria Syndrome

SAMMY-seq reveals early alteration of heterochromatin and deregulation of bivalent genes in Hutchinson-Gilford Progeria Syndrome

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Hutchinson-Gilford progeria Oven Door Lock syndrome is a genetic disease where an aberrant form of Lamin A disrupts chromatin by interfering with lamina associated domains.Here, the authors present the SAMMY-seq, a method for genome-wide characterization of heterochromatin dynamics and detect early stage alterations of heterochromatin structure in progeria Shower Commode Chairs primary fibroblasts, accompained by Polycomb dysfunctions.

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