Semi-quantitative RT-PCR method to estimate full-length mRNA levels of the multidrug resistance gene

Z. Yang, E. L. Woodahl, X. Y. Wang, T. Bui, D. D. Shen, R. J.Y. Ho

Research output: Contribution to journalArticlepeer-review


Expression levels of P-glycoprotein (P-gp), the transporter encoded by the human multidrug resistance gene (MDR1), may play an important role in drug disposition. The ability to quantitate full-length MDRI mRNA levels may be predictive of P-gp expression and function. Therefore, a semi-quantitative RT-PCR assay was developed to assess full-length MDR1 mRNA levels. Levels of full-length 3.8-kb MDR1 mRNA were estimated by comparing PCR amplification of the RNA extract with that of an internal standard, ΔMDR1. The 2.9-kb ΔMDR1 competitor RNA standard was constructed by deleting 965 bp from the interior of MDR1 mRNA. The full-length MDR1 and AMDR1 share identical 5′ and 3′ primer binding sequences, allowing for their simultaneous amplification in the same RT-PCR. With this approach, MDR1 mRNA levels can be sensitively and reliably estimated with a detection limit of 2000 copies. Full-length MDR1 mRNA levels in various human cell lines and lymphocytes from leukemia patients varied over 100-fold, ranging from 0.3 to 36.5 x 105 copies/μg total RNA. The semi-quantitative full-length RT-PCR assay may be useful in estimating MDR1 mRNA levels to assess P-gp expression, which may be important in studying the role of P-gp in drug disposition and cancer chemotherapy efficacy.

Original languageEnglish
Pages (from-to)196-203
Number of pages8
Issue number1
StatePublished - 2002


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