Evaluation of the Effects of DNase Treatment on Signal Specificity in RT-PCR and In Situ RT-PCR
Author(s) -
Karin Ivarsson,
Birgitta Weijdegård
Publication year - 1998
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/98254st04
Subject(s) - microbiology and biotechnology , dna , rna , biology , complementary dna , polymerase chain reaction , deoxyribonuclease i , multiple displacement amplification , reverse transcriptase , in situ , real time polymerase chain reaction , hybridization probe , chemistry , gene , biochemistry , base sequence , dna extraction , organic chemistry
In this study, the effects of DNase treatment on the specificity of reverse transcription (RT)-PCR have been investigated on different samples, containing RNA, DNA, DNA/RNA and DNA/cDNA. This was to evaluate the possibilities of getting specific results in a direct in situ RT-PCR. All DNA targets in the samples were eliminated after 1 h of DNase treatment. However, some DNA fragments still remained after both 1 h and overnight DNase treatment. When these fragments served as primers for amplification, nonspecific smears resulted. In samples containing small amounts of RNA, the RNA was affected by overnight treatment with DNase. Our conclusion is that the direct in situ RT-PCR is an unreliable method because the necessary DNase treatment induces nonspecific amplification, and no size-separation is possible. We conclude that the best way to perform an in situ RT-PCR is to hybridize with a labeled specific probe after amplification is completed.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom