Published online before print
January 14, 2003, 10.1101/gr.912603
Vol 13, Issue 2, 216-223, February 2003
LETTER
Global RNA Half-Life Analysis in Escherichia coli Reveals Positional Patterns of Transcript Degradation
Douglas W. Selinger1,3,
Rini Mukherjee Saxena2,3,
Kevin J. Cheung1,
George M. Church1 and
Carsten Rosenow2,4
1Harvard Medical School, Department of Genetics,
Boston, Massachusetts 02115, USA; 2Affymetrix Inc.,
Santa Clara, California 95051, USA
Subgenic-resolution oligonucleotide microarrays were used to study
global RNA degradation in wild-type Escherichia coli MG1655.
RNA chemical half-lives were measured for 1036 open reading frames
(ORFs) and for 329 known and predicted operons. The half-life of total
mRNA was 6.8 min under the conditions tested. We also observed
significant relationships between gene functional assignments and
transcript stability. Unexpectedly, transcription of a single operon
(tdcABCDEFG) was relatively rifampicin-insensitive and showed
significant increases 2.5 min after rifampicin addition. This supports
a novel mechanism of transcription for the tdc operon, whose
promoter lacks any recognizable binding sites. Probe by probe
analysis of all known and predicted operons showed that the 5' ends of
operons degrade, on average, more quickly than the rest of the
transcript, with stability increasing in a 3' direction, supporting and
further generalizing the current model of a net 5' to 3' directionality
of degradation. Hierarchical clustering analysis of operon degradation
patterns revealed that this pattern predominates but is not exclusive.
We found a weak but highly significant correlation between the
degradation of adjacent operon regions, suggesting that stability is
determined by a combination of local and operon-wide stability
determinants. The 16 ORF dcw gene cluster, which has a complex
promoter structure and a partially characterized degradation pattern,
was studied at high resolution, allowing a detailed and integrated
description of its abundance and degradation. We discuss the
application of subgenic resolution DNA microarray analysis to study
global mechanisms of RNA transcription and processing.
3 These authors contributed equally to this work.
4 Corresponding author.
E-MAIL carsten_rosenow{at}affymetrix.com; FAX (408) 481-0422.
Article and publication are at
http://www.genome.org/cgi/doi/10.1101/gr.912603. Article published online before print in January 2003.

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