Literature DB >> 31127577

Cellular Assays to Study the Functional Importance of Human DNA Repair Helicases.

Sanket Awate1, Srijita Dhar1, Joshua A Sommers1, Robert M Brosh2.   

Abstract

DNA helicases represent a specialized class of enzymes that play crucial roles in the DNA damage response. Using the energy of nucleoside triphosphate binding and hydrolysis, helicases behave as molecular motors capable of efficiently disrupting the many noncovalent hydrogen bonds that stabilize DNA molecules with secondary structure. In addition to their importance in DNA damage sensing and signaling, DNA helicases facilitate specific steps in DNA repair mechanisms that require polynucleotide tract unwinding or resolution. Because they play fundamental roles in the DNA damage response and DNA repair, defects in helicases disrupt cellular homeostasis. Thus, helicase deficiency or inhibition may result in reduced cell proliferation and survival, apoptosis, DNA damage induction, defective localization of repair proteins to sites of genomic DNA damage, chromosomal instability, and defective DNA repair pathways such as homologous recombination of double-strand breaks. In this chapter, we will describe step-by-step protocols to assay the functional importance of human DNA repair helicases in genome stability and cellular homeostasis.

Entities:  

Keywords:  DNA damage; DNA repair; Genetic disease; Genomic stability; Helicase; Replication stress

Mesh:

Substances:

Year:  2019        PMID: 31127577      PMCID: PMC9123881          DOI: 10.1007/978-1-4939-9500-4_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  42 in total

1.  Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest.

Authors:  A Constantinou; M Tarsounas; J K Karow; R M Brosh; V A Bohr; I D Hickson; S C West
Journal:  EMBO Rep       Date:  2000-07       Impact factor: 8.807

2.  FANCJ helicase defective in Fanconia anemia and breast cancer unwinds G-quadruplex DNA to defend genomic stability.

Authors:  Yuliang Wu; Kazuo Shin-ya; Robert M Brosh
Journal:  Mol Cell Biol       Date:  2008-04-21       Impact factor: 4.272

Review 3.  G4-Interacting DNA Helicases and Polymerases: Potential Therapeutic Targets.

Authors:  Katrina N Estep; Thomas J Butler; Jun Ding; Robert M Brosh
Journal:  Curr Med Chem       Date:  2019       Impact factor: 4.530

4.  RECQL1 and WRN proteins are potential therapeutic targets in head and neck squamous cell carcinoma.

Authors:  Akihito Arai; Tokuhiro Chano; Kazunobu Futami; Yasuhiro Furuichi; Kaichiro Ikebuchi; Takuma Inui; Hitosuke Tameno; Yasuko Ochi; Taketoshi Shimada; Yasuo Hisa; Hidetoshi Okabe
Journal:  Cancer Res       Date:  2011-05-13       Impact factor: 12.701

Review 5.  Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction.

Authors:  Michael V Berridge; Patries M Herst; An S Tan
Journal:  Biotechnol Annu Rev       Date:  2005

6.  Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome.

Authors:  Avvaru N Suhasini; Nina A Rawtani; Yuliang Wu; Joshua A Sommers; Sudha Sharma; Georgina Mosedale; Phillip S North; Sharon B Cantor; Ian D Hickson; Robert M Brosh
Journal:  EMBO J       Date:  2011-01-14       Impact factor: 11.598

Review 7.  DNA helicases, genomic instability, and human genetic disease.

Authors:  A J van Brabant; R Stan; N A Ellis
Journal:  Annu Rev Genomics Hum Genet       Date:  2000       Impact factor: 8.929

8.  Catalytic strand separation by RECQ1 is required for RPA-mediated response to replication stress.

Authors:  Taraswi Banerjee; Joshua A Sommers; Jing Huang; Michael M Seidman; Robert M Brosh
Journal:  Curr Biol       Date:  2015-10-08       Impact factor: 10.834

9.  Unwinding and rewinding: double faces of helicase?

Authors:  Yuliang Wu
Journal:  J Nucleic Acids       Date:  2012-07-19

Review 10.  Structural Mechanisms of Hexameric Helicase Loading, Assembly, and Unwinding.

Authors:  Michael A Trakselis
Journal:  F1000Res       Date:  2016-01-27
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  1 in total

1.  FANCJ compensates for RAP80 deficiency and suppresses genomic instability induced by interstrand cross-links.

Authors:  Sanket Awate; Joshua A Sommers; Arindam Datta; Sumeet Nayak; Marina A Bellani; Olivia Yang; Christopher A Dunn; Claudia M Nicolae; George-Lucian Moldovan; Michael M Seidman; Sharon B Cantor; Robert M Brosh
Journal:  Nucleic Acids Res       Date:  2020-09-18       Impact factor: 19.160

  1 in total

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