Home LiteratureArticle Details
PMID: 1979752 Published · ppublish English Comparative Study Journal Article

Use of the polymerase chain reaction in the quantitation of mdr-1 gene expression.

Biochemistry ·Vol. 29 ·No. 45 ·1990-11-13 ·Pages 10351-6

Murphy LD, Herzog CE, Rudick JB, Fojo AT, Bates SE

Abstract

The ability of the polymerase chain reaction (PCR) to quantitate expression of mRNA was examined in the present study. The model chosen was expression of the multidrug resistance gene mdr-1/Pgp in two colon carcinoma cell lines which express mdr-1/Pgp at levels comparable to those found in many clinical samples. PCR was utilized to evaluate differences in mdr-1/Pgp expression in the two cell lines after modulation by sodium butyrate. Thus, comparisons were made across a range of mdr-1/Pgp expression as well as comparisons of small differences. The PCR was found to be both sensitive and quantitative. Accurate quantitation requires demonstration of an exponential range which varies among samples. The exponential range can be determined by carrying out the PCR for a fixed number of cycles on serial dilutions of the RNA reverse transcription product, or by performing the reaction with a varying number of cycles on a fixed quantity of cDNA. By quantitation of the difference in PCR product derived from a given amount of RNA from the sodium butyrate treated and untreated cells, the difference in mRNA expression between samples can be determined. Normalization of the results can be achieved by independent amplification of a control gene, such as beta 2-microglobulin, when the latter is also evaluated in the exponential range. Simultaneous amplification of the control and target genes results in lower levels of PCR products due to competition, which varies from sample to sample. The PCR is thus a labor-intensive but sensitive method of quantitating gene expression in small samples of RNA.

Related Genes
MeSH Terms
ATP Binding Cassette Transporter, Subfamily B, Member 1 Butyrates/pharmacology Butyric Acid DNA/biosynthesis Deoxycytosine Nucleotides/metabolism Gene Expression/drug effects Humans Membrane Glycoproteins/genetics Polymerase Chain Reaction RNA, Messenger/biosynthesis Sensitivity and Specificity Transcription, Genetic Tumor Cells, Cultured
Chemicals
ATP Binding Cassette Transporter, Subfamily B, Member 1 Butyrates Deoxycytosine Nucleotides Membrane Glycoproteins RNA, Messenger Butyric Acid 2'-deoxycytidine 5'-triphosphate DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Murphy L D
Medicine Branch, National Cancer Institute, Bethesda, Maryland 20892.
Herzog C E
Rudick J B
Fojo A T
Bates S E
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1990-11-13
Pages
10351-6
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com