Nuclear organization and regulation of the differentiated state

Regulation of the differentiated identity requires active and continued supervision. Inability to maintain the differentiated state is a hallmark of aging and aging-related disease. To maintain cellular identity, a network of nuclear regulators is devoted to silencing previous and non-relevant gene programs. This network involves transcription factors, epigenetic regulators, and the localization of silent genes to heterochromatin. Together, identity supervisors mold and maintain the unique nuclear environment of the differentiated cell. This review describes recent discoveries regarding mechanisms and regulators that supervise the differentiated identity and protect from de-differentiation, tumorigenesis, and attenuate forced somatic cell reprograming. The review focuses on mechanisms involved in H3K9me3-decorated heterochromatin and the importance of nuclear lamins in cell identity. We outline how the biophysical properties of these factors are involved in self-compartmentalization of heterochromatin and cell identity. Finally, we discuss the relevance of these regulators to aging and age-related disease.

Automated summary

Active and continued supervision is required to regulate the differentiated identity, as inability to do so is a hallmark of aging and aging-related disease. A network of nuclear regulators, including transcription factors, epigenetic regulators, and the localization of silent genes, is dedicated to maintaining cellular identity. Recent discoveries focus on mechanisms involving H3K9me3-decorated heterochromatin and the importance of nuclear lamins in cell identity, with relevance to aging and age-related disease discussed.