Published online 23 November 2004
Nucleic Acids Research, Vol. 32 No. 20 © Oxford University Press 2004; all rights reserved
Systematic analysis of bicistronic reporter assay data
Department of Cell Biology and Molecular Genetics, 2135 Microbiology Building, University of Maryland, College Park, MD 20742, USA
* To whom correspondence should be addressed. Tel: +1 301 405 0918; Fax: +1 301 314 9489; Email: dinman{at}umd.edu
Received August 12, 2004; Revised October 6, 2004; Accepted October 29, 2004
Bicistronic reporter assay systems have become a mainstay of molecular biology. While the assays themselves encompass a broad range of diverse and unrelated experimental protocols, the numerical data garnered from these experiments often have similar statistical properties. In general, a primary dataset measures the paired expression of two internally controlled reporter genes. The expression ratio of these two genes is then normalized to an external control reporter. The end result is a ratio of ratios that is inherently sensitive to propagation of the error contributed by each of the respective numerical components. The statistical analysis of this data therefore requires careful handling in order to control for the propagation of error and its potentially misleading effects. A careful survey of the literature found no consistent method for the statistical analysis of data generated from these important and informative assay systems. In this report, we present a detailed statistical framework for the systematic analysis of data obtained from bicistronic reporter assay systems. Specifically, a dual luciferase reporter assay was employed to measure the efficiency of four programmed 1 frameshift signals. These frameshift signals originate from the L-A virus, the SARS-associated Coronavirus and computationally identified frameshift signals from two Saccharomyces cerevisiae genes. Furthermore, these statistical methods were applied to prove that the effects of anisomycin on programmed 1 frameshifting are statistically significant. A set of Microsoft Excel spreadsheets, which can be used as templates for data generated by dual reporter assay systems, and an online tutorial are available at our website (http://dinmanlab.umd.edu/statistics). These spreadsheets could be easily adapted to any bicistronic reporter assay system.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
P.-Y. Liao, P. Gupta, A. N. Petrov, J. D. Dinman, and K. H. Lee A new kinetic model reveals the synergistic effect of E-, P- and A-sites on +1 ribosomal frameshifting Nucleic Acids Res., May 1, 2008; 36(8): 2619 - 2629. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Meskauskas, J. R. Russ, and J. D. Dinman Structure/function analysis of yeast ribosomal protein L2 Nucleic Acids Res., April 1, 2008; 36(6): 1826 - 1835. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Rakauskaite and J. D. Dinman rRNA mutants in the yeast peptidyltransferase center reveal allosteric information networks and mechanisms of drug resistance Nucleic Acids Res., March 1, 2008; 36(5): 1497 - 1507. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Galkin, A. A. Bentley, S. Gupta, B.-A. Compton, B. Mazumder, T. G. Kinzy, W. C. Merrick, M. Hatzoglou, T. V. Pestova, C. U.T. Hellen, et al. Roles of the negatively charged N-terminal extension of Saccharomyces cerevisiae ribosomal protein S5 revealed by characterization of a yeast strain containing human ribosomal protein S5 RNA, December 1, 2007; 13(12): 2116 - 2128. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Jacobs, A. T. Belew, R. Rakauskaite, and J. D. Dinman Identification of functional, endogenous programmed -1 ribosomal frameshift signals in the genome of Saccharomyces cerevisiae Nucleic Acids Res., January 12, 2007; 35(1): 165 - 174. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Rakauskaite and J. D. Dinman An Arc of Unpaired "Hinge Bases" Facilitates Information Exchange among Functional Centers of the Ribosome Mol. Cell. Biol., December 1, 2006; 26(23): 8992 - 9002. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. L. Muldoon-Jacobs and J. D. Dinman Specific effects of ribosome-tethered molecular chaperones on programmed -1 ribosomal frameshifting. Eukaryot. Cell, April 1, 2006; 5(4): 762 - 770. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Meskauskas, A. N. Petrov, and J. D. Dinman Identification of Functionally Important Amino Acids of Ribosomal Protein L3 by Saturation Mutagenesis Mol. Cell. Biol., December 15, 2005; 25(24): 10863 - 10874. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. S. McNabb, R. Reed, and R. A. Marciniak Dual Luciferase Assay System for Rapid Assessment of Gene Expression in Saccharomyces cerevisiae Eukaryot. Cell, September 1, 2005; 4(9): 1539 - 1549. [Abstract] [Full Text] [PDF] |
||||



