Epigenetic-Mediated Regulation of Gene Expression for Biological Control and Cancer: Fidelity of Mechanisms Governing the Cell Cycle
Authors:
- Mohammed El DikaMDMohammed El Dika
- Andrew J. FritzAFAndrew J. Fritz
- Rabail H. ToorRTRabail H. Toor
- Princess D. RodriguezPRPrincess D. Rodriguez
- Stephen J. FoleySFStephen J. Foley
- Rahim UllahRURahim Ullah
- Daijing NieDNDaijing Nie
- Bodhisattwa BanerjeeBodhisattwa Banerjee
- Dorcas LoheseDLDorcas Lohese
- Kirsten M. TracyKTKirsten M. Tracy
- Karen C. GlassKGKaren C. Glass
- Seth FrietzeSeth Frietze
- 8 November 2022
- book chapter
- Published by Springer Nature
- Vol. 70, 375-396
Abstract
The cell cycle is governed by stringent epigenetic mechanisms that, in response to intrinsic and extrinsic regulatory cues, support fidelity of DNA replication and cell division. We will focus on (1) the complex and interdependent processes that are obligatory for control of proliferation and compromised in cancer, (2) epigenetic and topological domains that are associated with distinct phases of the cell cycle that may be altered in cancer initiation and progression, and (3) the requirement for mitotic bookmarking to maintain intranuclear localization of transcriptional regulatory machinery to reinforce cell identity throughout the cell cycle to prevent malignant transformation. Keywords Chromatin Nuclear structure Nucleosomes Histones Epigenetic control Mitotic gene bookmarking Transcription Cell cycle control Tumor suppressionKeywords
This publication has 141 references indexed in Scilit:
- Gene bookmarking accelerates the kinetics of post-mitotic transcriptional re-activationNature Cell Biology, 2011
- Repo-Man Coordinates Chromosomal Reorganization with Nuclear Envelope Reassembly during Mitotic ExitDevelopmental Cell, 2011
- A phospho/methyl switch at histone H3 regulates TFIID association with mitotic chromosomesThe EMBO Journal, 2010
- A mitotic transcriptional switch in polycystic kidney diseaseNature Medicine, 2009
- A Reconfigured Pattern of MLL Occupancy within Mitotic Chromatin Promotes Rapid Transcriptional Reactivation Following Mitotic ExitMolecular Cell, 2009
- Human embryonic stem cells are pre‐mitotically committed to self‐renewal and acquire a lengthened G1 phase upon lineage programmingJournal of Cellular Physiology, 2009
- 30 nm Chromatin Fibre Decompaction Requires both H4-K16 Acetylation and Linker Histone EvictionJournal of Molecular Biology, 2008
- Chromatin Modifications and Their FunctionCell, 2007
- The Histone Gene Transcription Factor HiNF-P Stabilizes Its Cell Cycle Regulatory Co-Activator p220NPATBiochemistry, 2006
- Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivoCell, 1995