Analysis of Oxidative Damage by Gene‐Specific Quantitative PCR

Current Protocols in Human Genetics - Tập 62 Số 1 - 2009
Olga A. Kovalenko1, Janine H. Santos1
1University of Medicine and Dentistry of New Jersey, Newark, New Jersey

Tóm tắt

AbstractThis unit describes the gene‐specific quantitative PCR‐based (QPCR) assay, which is used to measure DNA integrity of both nuclear and mitochondrial genomes based on amplification of long DNA targets. QPCR can be used to quantify the formation of DNA damage and the kinetics of DNA repair by following restoration of amplification of the target DNA over time after removal of the damaging agent. A detailed protocol to set up QPCR in any laboratory, highlighting critical parameters for successful establishment of the assay and interpretation of the results, is provided here. Advantages (e.g., the use of nanogram amounts of DNA) and limitations (e.g., the inability to define the specific type of lesion present on the DNA) of using QPCR to assay DNA damage in human cells are also described. Curr. Protoc. Hum. Genet. 62:19.1.1‐19.1.13. © 2009 by John Wiley & Sons, Inc.

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Tài liệu tham khảo

10.1385/1-59259-973-7:155

Ayala‐Torres S., 2000, Methods: A Companion to Methods in Enzymology, 135

10.1152/ajpgi.00044.2006

10.1161/01.CIR.0000023921.93743.89

10.1002/mrd.20285

10.1016/S0891-5849(02)00787-6

10.1016/j.freeradbiomed.2007.07.015

10.1016/S0027-5107(00)00014-2

10.1093/nar/26.8.2001

10.1081/CNV-120002155

10.1016/S0891-5849(02)00966-8

10.1111/j.1440-1746.2007.05277.x

10.1016/j.ymgme.2003.08.009

10.1124/mi.5.2.7

10.1126/science.287.5460.2017

10.2337/db08-0057

10.1074/jbc.M413022200

10.1093/nar/19.22.6209

10.1076/ceyr.23.1.11.5423

10.1093/nar/20.13.3485

10.1093/hmg/ddg349

10.1167/iovs.07-1607

10.1093/carcin/bgn250

10.1016/S0006-8993(00)02926-7

10.1152/ajpheart.2001.280.6.H2779

Ng F., 2008, Oxidative stress in psychiatric disorders: Evidence base and therapeutic implications, Int. J. Neuropsychopharmacol., 6, 851

10.1023/A:1017918330073

10.1016/j.taap.2004.06.021

10.1111/j.1440-1746.2006.04640.x

10.1038/3108

10.1093/nar/19.11.2929

10.1002/(SICI)1098-2744(199605)16:1<32::AID-MC5>3.0.CO;2-Q

Rezin G.T., 2008, Mitochondrial dysfunction and psychiatric disorders, Neurochem. Res.

10.1073/pnas.85.17.6465

10.1016/1357-2725(95)00025-K

Santos J.H., 2002, Measuring oxidative mtDNA damage and repair using quantitative PCR, Methods Mol. Biol., 197, 159

10.1074/jbc.M208752200

10.1111/j.1474-9728.2004.00124.x

10.1093/hmg/ddl098

10.1385/1-59259-973-7:183

10.1016/S0027-5107(03)00101-5

10.1152/ajplung.00038.2003

10.1073/pnas.092662499

10.1016/j.freeradbiomed.2008.05.014

10.1016/S0027-5107(00)00019-1

10.1073/pnas.85.11.3723

10.1016/S0027-5107(98)00076-1

Houten B., 1999, Mitochondrial DNA damage and repair, Mutat. Res., 434, 133

10.1016/j.dnarep.2005.03.002

10.1002/mrdd.1023

Wang A.L., 2008, Increased mitochondrial DNA damage and down‐regulation of DNA repair enzymes in aged rodent retinal pigment epithelium and choroid, Mol. Vis., 14, 644

Yanez J.A., 2003, Chemotherapy induced gastrointestinal toxicity in rats: Involvement of mitochondrial DNA, gastrointestinal permeability and cyclooxygenase‐2, J. Pharm. Pharm. Sci., 6, 308

10.1016/j.dnarep.2008.03.012