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DNA laddering
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DNA laddering is a feature that can be observed when DNA fragments, resulting from apoptotic DNA fragmentation, are visualized after separation by gel electrophoresis. It was first described in 1980 by Andrew Wyllie at the University of Edinburgh Medical School.[1] DNA fragments can also be detected in cells that underwent necrosis, but when these DNA fragments are visualized after separation there is no clear "ladder" pattern present. [1]
DNA laddering is a distinctive feature of DNA degraded by caspase-activated DNase (CAD), which is a key event during apoptosis. CAD cleaves genomic DNA at internucleosomal linker regions, resulting in DNA fragments that are multiples of 180–185 base-pairs in length.[2] Separation of the fragments by agarose gel electrophoresis and subsequent visualization, for example by ethidium bromide staining, results in a characteristic "ladder" pattern.(Needs a citation)
While most of the morphological features of apoptotic cells are short-lived, DNA laddering can be used as final state read-out method and has therefore become a reliable method to distinguish apoptosis from necrosis.[2] DNA laddering can also be used to see if cells underwent apoptosis in the presence of a virus. [3] This is useful because it can help determine the effects a virus has on a cell.
DNA laddering can only be used to detect apoptosis during the later stages of apoptosis. This is due to DNA fragmentation taking place in a later stage of the apoptosis process.[2] DNA laddering is used to test for apoptosis of many cells, and is not accurate at testing for only a few cells that committed apoptosis. [2] To enhance the accuracy in testing for apoptosis, other assays are used along with DNA laddering such as TEM and TUNEL. [2] With recent improvements to DNA laddering, DNA laddering has become a more reliable, and reasonable technique to use when detecting apoptosis.[4] It is also important to note that DNA laddering occurs differently depending on the type of cell, so there may be slight changes in the process of DNA laddering depending on the cell that is being investigated. [5]
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[edit]Further reading[edit | edit source]
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- ^ Kressel, M.; Groscurth, P. (1994-12-01). "Distinction of apoptotic and necrotic cell death by in situ labelling of fragmented DNA". Cell and Tissue Research. 278 (3): 549–556. ISSN 0302-766X. PMID 7850865.
- ^ a b c d Elmore, Susan. "Apoptosis: A Review of Programmed Cell Death". Toxicol Pathol. 35(4).
- ^ Srivastava, Vikram; Rawall, Shweta; Vijayan, V. K.; Khanna, Madhu (2009-05-01). "Influenza a virus induced apoptosis: inhibition of DNA laddering & caspase-3 activity by zinc supplementation in cultured HeLa cells". The Indian Journal of Medical Research. 129 (5): 579–586. ISSN 0971-5916. PMID 19675388.
- ^ Rahbar Saadat, Yalda; Saeidi, Nazli; Zununi Vahed, Sepideh; Barzegari, Abolfazl; Barar, Jaleh (2015-01-01). "An update to DNA ladder assay for apoptosis detection". BioImpacts : BI. 5 (1): 25–28. doi:10.15171/bi.2015.01. ISSN 2228-5652. PMC 4401164. PMID 25901294.
- ^ Jiang, Ai-Liang; Cheng, Yanwei; Li, Jianyou; Zhang, Wei (2008-07-31). "A zinc-dependent nuclear endonuclease is responsible for DNA laddering during salt-induced programmed cell death in root tip cells of rice". Journal of Plant Physiology. 165 (11): 1134–1141. doi:10.1016/j.jplph.2007.12.008. ISSN 1618-1328. PMID 18295371.