The comet assay as a method of identifying chromosomes instability
Journal Title: Advances in Hygiene and Experimental Medicine - Year 2014, Vol 68, Issue
Abstract
The basic method for analyzing the degree of DNA fragmentation caused by genotoxic factors is gel electrophoresis of single cells (single cell gel electrophoresis), also called the comet assay. The comet assay enables the analysis of the level of several different DNA modifications. The basic testing procedure has been only slightly modified. This method helps identify single-strand and double-strand DNA cracks, as well as any chemical and enzymatic modifications that can potentially turn into cracks in DNA or chromatids. The comet assay makes it possible to detect DNA damage at the level of single cells. It can be employed in analyses of any tissues which provide cellular suspensions. Analysed cells are submerged in agarose on a microscope slide. DNA is what is left after proteins have been broken down. The slide is then subjected to electrophoresis and stained with a fluorescent dye. A “comet-like” image is obtained. The “head” is the cell fixation site prior to lysis; the “tail” represents damaged DNA fragments. The extent of DNA damage is reflected in the length of the tail and the amount of DNA contained in it. The assay finds research applications in the following fields: genetic toxicology, monitoring of DNA repair following chemotherapy and radiotherapy, ecotoxicology, animal and human nourishment, biomonitoring of genotoxicity, epidemiology and assessment of material deposited in sperm and blood banks.
Authors and Affiliations
Magdalena Czubaszek, Małgorzata Szostek, Ewa Wójcik, Katarzyna Andraszek
Prevalence of Helicobacter pylori cagA, vacA, iceA, babA2 genotypes in Polish children and adolescents with gastroduodenal disease
Introduction: Infection with Helicobacter pylori is a major cause of chronic gastritis and peptic ulcer disease in children and its consequences in adulthood can lead to serious complications, including in particular the...
Rola ceramidów w wybranych patologiach mózgu: ischemia/hipoksja, choroba Alzheimera
Ceramidy z grupy sfingolipidów, powstają w ośrodkowym układzie nerwowym w wyniku syntezy de novo, za pośrednictwem hydrolizy sfingomieliny lub w tzw. „szlaku ratunkowym”. Biorą udział w tworzeniu tratw lipidowych, które...
Rola nutrigenomiki we wspomaganiu leczenia otyłości
Otyłość i nadwaga to wciąż narastający problem zdrowotny i społeczny. Obecnie duże nadzieje w walce z otyłością i nadwagą, wiążę się z nową dyscypliną nauki jaką jest nutrigenomika (i/lub nutrigenetyka). Nutrigenomika, w...
Enterobacteriaceae infection – diagnosis, antibiotic resistance and prevention
Intestinal infections caused by rod-shaped bacteria of the [i]Enterobacteriaceae[/i] genus are one of the major health hazards in countries where sanitation standards are low. [i]Strains[/i] of [i]Shigella,[/i] [i]Salm...
Mutacje w genie PKD1 - wpływ na obraz kliniczny pacjentów ze zwyrodnieniem wielotorbielowatym nerek z Dolnego Śląska
Wprowadzenie: Autosomalna, dominująca postać zwyrodnienia torbielowatego nerek (ADPKD) jest jedną z najczęstszych schorzeń genetycznych, charakteryzująca się rozwojem niezliczonej liczby, różnej wielkości torbieli w korz...