Firefly luciferase gene contains a cryptic promoter

  1. Václav Vopálenský1,3,
  2. Tomáš Mašek1,3,
  3. Ondřej Horváth2,
  4. Blanka Vicenová1,
  5. Martin Mokrejš1, and
  6. Martin Pospíšek1
  1. 1Department of Genetics and Microbiology, Faculty of Science, Charles University in Prague, Vinicna 5, 128 44 Prague, Czech Republic
  2. 2Institute of Molecular Genetics, Laboratory of Leukocyte Antigens, AS CR, Videnska 1083, 140 00 Prague, Czech Republic
  1. 3 These authors contributed equally to this work.

Abstract

Firefly luciferase (FLuc) counts among the most popular reporters of present-day molecular and cellular biology. In this study, we report a cryptic promoter activity in the luc+ gene, which is the most frequently used version of firefly luciferase. The FLuc coding region displays cryptic promoter activity both in mammalian and yeast cells. In human CCL13 and Huh7 cells, cryptic transcription from the luc+ gene is 10–16 times weaker in comparison to the strong immediate-early cytomegalovirus promoter. Additionally, we discuss a possible impact of the FLuc gene cryptic promoter on experimental results especially in some fields of the RNA-oriented research, for example, in analysis of translation initiation or analysis of miRNA/siRNA function. Specifically, we propose how this newly described cryptic promoter activity within the FLuc gene may contribute to the previous determination of the strength of the cryptic promoter found in the cDNA corresponding to the hepatitis C virus internal ribosome entry site. Our findings should appeal to the researchers when taking care of designing firefly luciferase-based assays as well as opening the possibility of performing some experiments with the hepatitis C virus internal ribosome entry site, which could not be considered until now.

Keywords

Footnotes

  • Reprint requests to: Martin Pospíšek, Department of Genetics and Microbiology, Faculty of Science, Charles University in Prague, Vinicna 5, 128 44 Prague, Czech Republic; e-mail: martin{at}natur.cuni.cz; fax: 420-2-221951724.

  • Article and publication are at http://www.rnajournal.org/cgi/doi/10.1261/rna.831808.

    • Received September 19, 2007.
    • Accepted June 5, 2008.

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