Literature DB >> 33682029

Who gets a license: DNA synthesis in quiescent cells re-entering the cell cycle.

Po-Hsuen Lee1, Mary Ann Osley2.   

Abstract

The precise regulation of the entry into S phase is critical for preventing genome instability. The first step in the initiation of eukaryotic DNA synthesis occurs in G1 phase cells and involves the loading of the conserved MCM helicase onto multiple origins of replication in a process known as origin licensing. In proliferating metazoan cells, an origin-licensing checkpoint delays initiation until high levels of MCM loading occur, with excess origins being licensed. One function of this checkpoint is to ensure that S phase can be completed in the face of replication stress by activation of dormant MCM bound origins. However, when both metazoan and yeast cells enter S phase from quiescence or G0 phase, a non-growing but reversible cell cycle state, origins are significantly under-licensed. In metazoan cells, under-licensing is the result of a compromised origin-licensing checkpoint. In budding yeast, our study has revealed that under-licensing can be attributed to the chromatin structure at a class of origins that is inhibitory to the binding of MCM. Thus, defects in multiple pathways may contribute to the failure to fully license origins in quiescent cells re-entering the cell cycle, thereby promoting a higher risk of genome instability.

Entities:  

Keywords:  Cell cycle; Chromatin structure; Origin licensing; Quiescent cells

Mesh:

Substances:

Year:  2021        PMID: 33682029      PMCID: PMC8254781          DOI: 10.1007/s00294-021-01170-7

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   2.695


  43 in total

1.  Activation of dormant origins of DNA replication in budding yeast.

Authors:  C Santocanale; K Sharma; J F Diffley
Journal:  Genes Dev       Date:  1999-09-15       Impact factor: 11.361

2.  ORC and the intra-S-phase checkpoint: a threshold regulates Rad53p activation in S phase.

Authors:  Kenji Shimada; Philippe Pasero; Susan M Gasser
Journal:  Genes Dev       Date:  2002-12-15       Impact factor: 11.361

3.  Dormant origins licensed by excess Mcm2-7 are required for human cells to survive replicative stress.

Authors:  Xin Quan Ge; Dean A Jackson; J Julian Blow
Journal:  Genes Dev       Date:  2007-12-15       Impact factor: 11.361

4.  Condensin-Dependent Chromatin Compaction Represses Transcription Globally during Quiescence.

Authors:  Sarah G Swygert; Seungsoo Kim; Xiaoying Wu; Tianhong Fu; Tsung-Han Hsieh; Oliver J Rando; Robert N Eisenman; Jay Shendure; Jeffrey N McKnight; Toshio Tsukiyama
Journal:  Mol Cell       Date:  2018-12-27       Impact factor: 17.970

Review 5.  Chromosome Duplication in Saccharomyces cerevisiae.

Authors:  Stephen P Bell; Karim Labib
Journal:  Genetics       Date:  2016-07       Impact factor: 4.562

6.  OriDB: a DNA replication origin database.

Authors:  Conrad A Nieduszynski; Shin-ichiro Hiraga; Prashanth Ak; Craig J Benham; Anne D Donaldson
Journal:  Nucleic Acids Res       Date:  2006-10-25       Impact factor: 16.971

7.  Excess Mcm2-7 license dormant origins of replication that can be used under conditions of replicative stress.

Authors:  Anna M Woodward; Thomas Göhler; M Gloria Luciani; Maren Oehlmann; Xinquan Ge; Anton Gartner; Dean A Jackson; J Julian Blow
Journal:  J Cell Biol       Date:  2006-06-05       Impact factor: 10.539

8.  The chromatin environment shapes DNA replication origin organization and defines origin classes.

Authors:  Christelle Cayrou; Benoit Ballester; Isabelle Peiffer; Romain Fenouil; Philippe Coulombe; Jean-Christophe Andrau; Jacques van Helden; Marcel Méchali
Journal:  Genome Res       Date:  2015-11-11       Impact factor: 9.043

Review 9.  Dormant origins, the licensing checkpoint, and the response to replicative stresses.

Authors:  Debbie McIntosh; J Julian Blow
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-10-01       Impact factor: 10.005

10.  Replication stress caused by low MCM expression limits fetal erythropoiesis and hematopoietic stem cell functionality.

Authors:  Silvia Alvarez; Marcos Díaz; Johanna Flach; Sara Rodriguez-Acebes; Andrés J López-Contreras; Dolores Martínez; Marta Cañamero; Oscar Fernández-Capetillo; Joan Isern; Emmanuelle Passegué; Juan Méndez
Journal:  Nat Commun       Date:  2015-10-12       Impact factor: 14.919

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  1 in total

1.  Disruption of Toxoplasma gondii-Induced Host Cell DNA Replication Is Dependent on Contact Inhibition and Host Cell Type.

Authors:  Edwin Pierre-Louis; Menna G Etheridge; Rodrigo de Paula Baptista; Asis Khan; Nathan M Chasen; Ronald D Etheridge
Journal:  mSphere       Date:  2022-05-19       Impact factor: 5.029

  1 in total

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