Literature DB >> 32219379

How do cells sense DNA lesions?

Chiara Vittoria Colombo1, Marco Gnugnoli1, Elisa Gobbini1, Maria Pia Longhese1.   

Abstract

DNA is exposed to both endogenous and exogenous DNA damaging agents that chemically modify it. To counteract the deleterious effects exerted by DNA lesions, eukaryotic cells have evolved a network of cellular pathways, termed DNA damage response (DDR). The DDR comprises both mechanisms devoted to repair DNA lesions and signal transduction pathways that sense DNA damage and transduce this information to specific cellular targets. These targets, in turn, impact a wide range of cellular processes including DNA replication, DNA repair and cell cycle transitions. The importance of the DDR is highlighted by the fact that DDR inactivation is commonly found in cancer and causes many different human diseases. The protein kinases ATM and ATR, as well as their budding yeast orthologs Tel1 and Mec1, act as master regulators of the DDR. The initiating events in the DDR entail both DNA lesion recognition and assembly of protein complexes at the damaged DNA sites. Here, we review what is known about the early steps of the DDR.
© 2020 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.

Entities:  

Keywords:  ATM; ATR; DNA damage response; DNA recombination; DNA repair; single-stranded DNA

Mesh:

Substances:

Year:  2020        PMID: 32219379     DOI: 10.1042/BST20191118

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  4 in total

1.  The TIP60-ATM axis regulates replication fork stability in BRCA-deficient cells.

Authors:  Emily M Schleicher; Ashna Dhoonmoon; Lindsey M Jackson; Jude B Khatib; Claudia M Nicolae; George-Lucian Moldovan
Journal:  Oncogenesis       Date:  2022-06-18       Impact factor: 6.524

2.  An Inducible System for Silencing Establishment Reveals a Stepwise Mechanism in Which Anchoring at the Nuclear Periphery Precedes Heterochromatin Formation.

Authors:  Isabelle Loïodice; Mickael Garnier; Ivaylo Nikolov; Angela Taddei
Journal:  Cells       Date:  2021-10-20       Impact factor: 6.600

3.  Complementary CRISPR genome-wide genetic screens in PARP10-knockout and overexpressing cells identify synthetic interactions for PARP10-mediated cellular survival.

Authors:  Jude B Khatib; Emily M Schleicher; Lindsey M Jackson; Ashna Dhoonmoon; George-Lucian Moldovan; Claudia M Nicolae
Journal:  Oncotarget       Date:  2022-09-28

4.  Enzymatic bypass of an N6-deoxyadenosine DNA-ethylene dibromide-peptide crosslink by translesion DNA polymerases.

Authors:  Pratibha P Ghodke; Gabriela Gonzalez-Vasquez; Hui Wang; Kevin M Johnson; Carl A Sedgeman; F Peter Guengerich
Journal:  J Biol Chem       Date:  2021-02-19       Impact factor: 5.157

  4 in total

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