Author
Listed:
- Paula Montero Llopis
(Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA)
- Audrey F. Jackson
(Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
Current address: Cutaneous Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, USA.)
- Oleksii Sliusarenko
(Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520, USA)
- Ivan Surovtsev
(Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520, USA)
- Jennifer Heinritz
(Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520, USA)
- Thierry Emonet
(Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
Yale University, New Haven, Connecticut 06520, USA)
- Christine Jacobs-Wagner
(Cellular and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA
Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06520, USA
Section of Microbial Pathogenesis, Yale School of Medicine, New Haven, Connecticut 06510, USA)
Abstract
Eukaryotic cells spatially organize mRNA processes such as translation and mRNA decay. Much less is clear in bacterial cells where the spatial distribution of mature mRNA remains ambiguous. Using a sensitive method based on quantitative fluorescence in situ hybridization, we show here that in Caulobacter crescentus and Escherichia coli, chromosomally expressed mRNAs largely display limited dispersion from their site of transcription during their lifetime. We estimate apparent diffusion coefficients at least two orders of magnitude lower than expected for freely diffusing mRNA, and provide evidence in C. crescentus that this mRNA localization restricts ribosomal mobility. Furthermore, C. crescentus RNase E appears associated with the DNA independently of its mRNA substrates. Collectively, our findings show that bacteria can spatially organize translation and, potentially, mRNA decay by using the chromosome layout as a template. This chromosome-centric organization has important implications for cellular physiology and for our understanding of gene expression in bacteria.
Suggested Citation
Paula Montero Llopis & Audrey F. Jackson & Oleksii Sliusarenko & Ivan Surovtsev & Jennifer Heinritz & Thierry Emonet & Christine Jacobs-Wagner, 2010.
"Spatial organization of the flow of genetic information in bacteria,"
Nature, Nature, vol. 466(7302), pages 77-81, July.
Handle:
RePEc:nat:nature:v:466:y:2010:i:7302:d:10.1038_nature09152
DOI: 10.1038/nature09152
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