Competitive reverse transcription polymerase chain reaction for the quantification of p53 and mdm2 mRNA expression

被引:20
作者
Totzke, G [1 ]
Sachinidis, A [1 ]
Vetter, H [1 ]
Ko, Y [1 ]
机构
[1] UNIV BONN,MED POLIKLIN,D-53111 BONN,GERMANY
关键词
competitive RT/PCR; p53; mdm2;
D O I
10.1006/mcpr.1996.0059
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Wild-type p53 (wtp53) is a tumour suppressor gene involved in cell cycle regulation. The mdm2 protein can complex with the p53 protein and influence its function as a regulator of cell growth. To detect and quantify wtp53 and mdm2 mRNA expression, we established the competitive reverse transcription/polymerase chain reaction for these genes and for the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The target RNA differed from the competitor cRNA by having 183 bp, 205 bp and 173 bp deletions for p53, mdm2 and GAPDH, respectively. Target RNA and known concentrations of competitor cRNA were co-reverse transcribed and coamplified with the same primers. Target cDNA and the corresponding competitor cDNA were amplified at the same efficiency. (C) 1996 Academic Press Limited
引用
收藏
页码:427 / 433
页数:7
相关论文
共 20 条
[1]  
Andus Tilo, 1993, Regional Immunology, V5, P11
[2]   ABSOLUTE MESSENGER-RNA QUANTIFICATION USING THE POLYMERASE CHAIN-REACTION (PCR) - A NOVEL-APPROACH BY A PCR AIDED TRANSCRIPT TITRATION ASSAY (PATTY) [J].
BECKERANDRE, M ;
HAHLBROCK, K .
NUCLEIC ACIDS RESEARCH, 1989, 17 (22) :9437-9446
[3]   MOLECULAR ANALYSIS AND CHROMOSOMAL MAPPING OF AMPLIFIED GENES ISOLATED FROM A TRANSFORMED MOUSE 3T3-CELL LINE [J].
CAHILLYSNYDER, L ;
YANGFENG, T ;
FRANCKE, U ;
GEORGE, DL .
SOMATIC CELL AND MOLECULAR GENETICS, 1987, 13 (03) :235-244
[4]   TRANSCRIPTION OF THE DYSTROPHIN GENE IN HUMAN-MUSCLE AND NON-MUSCLE TISSUES [J].
CHELLY, J ;
KAPLAN, JC ;
MAIRE, P ;
GAUTRON, S ;
KAHN, A .
NATURE, 1988, 333 (6176) :858-860
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   A NOVEL PROCEDURE FOR QUANTITATIVE POLYMERASE CHAIN-REACTION BY COAMPLIFICATION OF COMPETITIVE TEMPLATES [J].
DIVIACCO, S ;
NORIO, P ;
ZENTILIN, L ;
MENZO, S ;
CLEMENTI, M ;
BIAMONTI, G ;
RIVA, S ;
FALASCHI, A ;
GIACCA, M .
GENE, 1992, 122 (02) :313-320
[7]   TUMORIGENIC POTENTIAL ASSOCIATED WITH ENHANCED EXPRESSION OF A GENE THAT IS AMPLIFIED IN A MOUSE-TUMOR CELL-LINE [J].
FAKHARZADEH, SS ;
TRUSKO, SP ;
GEORGE, DL .
EMBO JOURNAL, 1991, 10 (06) :1565-1569
[8]   ANALYSIS OF CYTOKINE MESSENGER-RNA AND DNA - DETECTION AND QUANTITATION BY COMPETITIVE POLYMERASE CHAIN-REACTION [J].
GILLILAND, G ;
PERRIN, S ;
BLANCHARD, K ;
BUNN, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) :2725-2729
[9]   MICRODIVERSITY OF HUMAN-PLASMA-MEMBRANE CALCIUM-PUMP ISOFORM-2 GENERATED BY ALTERNATIVE RNA SPLICING IN THE N-TERMINAL CODING REGION [J].
HEIM, R ;
HUG, M ;
IWATA, T ;
STREHLER, EE ;
CARAFOLI, E .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 205 (01) :333-340
[10]  
KASHANISABET M, 1988, CANCER RES, V48, P5775