Molecular Biology and Genetics

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 7 No. 1, Issue of April 15, 2004
© 2004 by Pontificia Universidad Católica de Valparaíso -- Chile Received October 13, 2003 / Accepted March 18, 2004
RESEARCH ARTICLE

Quantitative real-time PCR method to detect changes in specific transcript and total RNA amounts

Kwang-Hyun Baek
Department of Crop and Soil Sciences
210 Johnson Hall
Washington State University
Pullman, WA 99164-6420 USA
Tel: 01 509 335 3632
Fax: 1 509 335 2553
E-mail: kwanghyunbaek@wsu.edu 

Daniel Z. Skinner*
USDA-ARS & Department of Crop and Soil Sciences
209 Johnson Hall
Washington State University
Pullman, WA 99164-6420 USA
Tel 1 509 335 8696
Fax: 1 509 335 2553
E-mail:dzs@wsu.edu

*Corresponding author


Financial support: USDA-Agricultural Research Service.

Keywords: cold treatment, quantitative real-time PCR, total RNA, wheat.

Abbreviations:       RNA: ribonucleic acid

                             qRT-PCR: quantitative real-time PCR

                             MnSOD: Manganese-dependent Superoxide dismutase

                             PLD: Phospholipase D

                             DEPC: diethyl pyrocarbonate

Abstract
Full Text

Quantitative real-time PCR (qRT-PCR), used in conjunction with reverse transcriptase, has been applied to the determination of the number of copies of a transcript per unit mass of RNA, but did not indicate any change in the amount of total RNA per mass of tissue. In the present work, we described a simple method to use qRT-PCR to estimate the change in the amount of total RNA per unit mass of wheat (Triticum aestivum L.) tissue in response to cold temperature. Three qRT-PCR templates, i.e. control, cold-exposed, and one of RNA extracted from a sample consisting of equal masses of control and cold-exposed tissue, were analyzed. The number of copies of target transcript per unit mass of RNA was estimated from the three samples using standard qRT-PCR techniques. Equations describing the number of copies of the target sequence in each of the tissue samples were solved simultaneously to describe the relative proportion of the target sequence that originated from each tissue sample in the mixture, thereby providing an estimate of relative amounts of total RNA in the two tissues.

 
Supported by UNESCO / MIRCEN network