Literature DB >> 16766222

The fast halo assay: an improved method to quantify genomic DNA strand breakage at the single-cell level.

Piero Sestili1, Chiara Martinelli, Vilberto Stocchi.   

Abstract

The present study describes the improvement of a technique, the alkaline-halo assay (AHA), for the assessment of DNA single-strand breakage at the single-cell level. AHA involves a series of sequential steps in which cells are embedded in melted agarose and spread onto microscope slides, incubated in a high-salt alkaline lysis solution, then in a hypotonic alkaline solution and, finally, stained with ethidium bromide (EB). Under these conditions, single-stranded DNA fragments diffuse radially from the nuclear cage and generate a fluorescent image that resembles a halo concentric to the nuclear remnants: the area of the halo is a direct function of the extent of DNA strand scission. These phenomena can be conveniently monitored with a fluorescence microscope and quantified by image-processing analysis. The behaviour of single-stranded DNA fragments under the conditions of the modified assay, called fast halo assay (FHA), is essentially the same as in AHA. The modifications consist in the simplification of the lysis, denaturation and staining procedures, and allow, as compared with AHA, the preparation of samples within 15 min, with a two-third reduction in total processing time, using only two reagents to promote DNA extraction and staining: NaOH and EB. A variation of the FHA operating at non-denaturing conditions to discriminate apoptotic cells from non-apoptotic cells bearing DNA single-strand breaks is also illustrated. To benchmark FHA sensitivity and reliability, the DNA single-strand breaks (SSBs) resulting either from exposure of cultured mammalian cells to different DNA-damaging agents or from secondary apoptotic DNA cleavage, have been quantified and results compared with the outcomes of reference techniques run in parallel, namely AHA, comet assay and Hoechst 33342 staining. The results indicate that FHA has the same reliability and sensitivity of the reference assays, but presents the additional advantages of being inexpensive, more rapid and strikingly simple.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16766222     DOI: 10.1016/j.mrgentox.2006.04.018

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  11 in total

1.  Molecular damage and induction of proinflammatory cytokines in human endothelial cells exposed to Shiga toxin 1, Shiga toxin 2, and alpha-sarcin.

Authors:  Maurizio Brigotti; Domenica Carnicelli; Elisa Ravanelli; Antonio González Vara; Chiara Martinelli; Roberta R Alfieri; Pier Giorgio Petronini; Piero Sestili
Journal:  Infect Immun       Date:  2007-02-12       Impact factor: 3.441

2.  Nuclear tau, a key player in neuronal DNA protection.

Authors:  Audrey Sultan; Fabrice Nesslany; Marie Violet; Séverine Bégard; Anne Loyens; Smail Talahari; Zeyni Mansuroglu; Daniel Marzin; Nicolas Sergeant; Sandrine Humez; Morvane Colin; Eliette Bonnefoy; Luc Buée; Marie-Christine Galas
Journal:  J Biol Chem       Date:  2010-12-03       Impact factor: 5.157

3.  Detection of DNA Damage in Hematopoietic Stem Cells.

Authors:  Saipriya Ayyar; Isabel Beerman
Journal:  Methods Mol Biol       Date:  2023

4.  Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?

Authors:  Ryuki Hirano; Heidrun Interthal; Cheng Huang; Tomonori Nakamura; Kimiko Deguchi; Kunho Choi; Meenakshi B Bhattacharjee; Kimiyoshi Arimura; Fujio Umehara; Shuji Izumo; Jennifer L Northrop; Mustafa A M Salih; Ken Inoue; Dawna L Armstrong; James J Champoux; Hiroshi Takashima; Cornelius F Boerkoel
Journal:  EMBO J       Date:  2007-10-18       Impact factor: 11.598

5.  NLRP3 inhibitor glibenclamide attenuates high-fat diet and streptozotocin-induced non-alcoholic fatty liver disease in rat: studies on oxidative stress, inflammation, DNA damage and insulin signalling pathway.

Authors:  Durgesh Kumar Dwivedi; G B Jena
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2019-12-13       Impact factor: 3.000

6.  Shiga toxin 1, as DNA repair inhibitor, synergistically potentiates the activity of the anticancer drug, mafosfamide, on raji cells.

Authors:  Maurizio Brigotti; Valentina Arfilli; Domenica Carnicelli; Laura Rocchi; Cinzia Calcabrini; Francesca Ricci; Pasqualepaolo Pagliaro; Pier Luigi Tazzari; Roberta R Alfieri; Pier Giorgio Petronini; Piero Sestili
Journal:  Toxins (Basel)       Date:  2013-02-21       Impact factor: 4.546

7.  Molecular mechanisms of ultraviolet radiation-induced DNA damage and repair.

Authors:  Rajesh P Rastogi; Ashok Kumar; Madhu B Tyagi; Rajeshwar P Sinha
Journal:  J Nucleic Acids       Date:  2010-12-16

8.  Deuterium Incorporation Protects Cells from Oxidative Damage.

Authors:  Piero Sestili; Maurizio Brigotti; Cinzia Calcabrini; Eleonora Turrini; Valentina Arfilli; Domenica Carnicelli; Marco Lucarini; Andrea Mazzanti; Andrea Milelli; Valeria Righi; Carmela Fimognari
Journal:  Oxid Med Cell Longev       Date:  2019-07-18       Impact factor: 6.543

9.  REC-2006-A Fractionated Extract of Podophyllum hexandrum Protects Cellular DNA from Radiation-Induced Damage by Reducing the Initial Damage and Enhancing Its Repair In Vivo.

Authors:  Pankaj Chaudhary; Sandeep Kumar Shukla; Rakesh Kumar Sharma
Journal:  Evid Based Complement Alternat Med       Date:  2011-06-16       Impact factor: 2.629

10.  Antileukemic activity of sulforaphane in primary blasts from patients affected by myelo- and lympho-proliferative disorders and in hypoxic conditions.

Authors:  Carmela Fimognari; Eleonora Turrini; Piero Sestili; Cinzia Calcabrini; Giovanni Carulli; Giulia Fontanelli; Martina Rousseau; Giorgio Cantelli-Forti; Patrizia Hrelia
Journal:  PLoS One       Date:  2014-07-14       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.