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Open Access Highly Accessed Methodology article

Absolute quantification of the budding yeast transcriptome by means of competitive PCR between genomic and complementary DNAs

Fumihito Miura12, Noriko Kawaguchi12, Mikio Yoshida23, Chihiro Uematsu4, Keiji Kito12, Yoshiyuki Sakaki5 and Takashi Ito12*

Author Affiliations

1 Department of Computational Biology, Graduate School of Frontier Sciences, University of Tokyo, Kashiwa 277-8561, Japan

2 Institute for Bioinformatics Research and Development (BIRD), Japan Science and Technology Agency (JST), Tokyo 102-0081, Japan

3 INTEC Systems Institute, Inc, Tokyo 136-0075, Japan

4 Central Research Laboratory, Hitachi, Ltd, Kokubunji 185-8601, Japan

5 RIKEN Genomic Sciences Center, Yokohama 230-0045, Japan

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BMC Genomics 2008, 9:574  doi:10.1186/1471-2164-9-574

Published: 29 November 2008

Abstract

Background

An ideal format to describe transcriptome would be its composition measured on the scale of absolute numbers of individual mRNAs per cell. It would help not only to precisely grasp the structure of the transcriptome but also to accelerate data exchange and integration.

Results

We conceived an idea of competitive PCR between genomic DNA and cDNA. Since the former contains every gene exactly at the same copy number, it can serve as an ideal normalization standard for the latter to obtain stoichiometric composition data of the transcriptome. This data can then be easily converted to absolute quantification data provided with an appropriate calibration. To implement this idea, we improved adaptor-tagged competitive PCR, originally developed for relative quantification of the 3'-end restriction fragment of each cDNA, such that it can be applied to any restriction fragment. We demonstrated that this "generalized" adaptor-tagged competitive PCR (GATC-PCR) can be performed between genomic DNA and cDNA to accurately measure absolute expression level of each mRNA in the budding yeast Saccharomyces cerevisiae. Furthermore, we constructed a large-scale GATC-PCR system to measure absolute expression levels of 5,038 genes to show that the yeast contains more than 30,000 copies of mRNA molecules per cell.

Conclusion

We developed a GATC-PCR method to accurately measure absolute expression levels of mRNAs by means of competitive amplification of genomic and cDNA copies of each gene. A large-scale application of GATC-PCR to the budding yeast transcriptome revealed that it is twice or more as large as previously estimated. This method is flexibly applicable to both targeted and genome-wide analyses of absolute expression levels of mRNAs.