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Title: The Transcription Unit Architecture of the Escherichia Coli Genome

Journal Article · · Nature Biotechnology
DOI:https://doi.org/10.1038/nbt.1582· OSTI ID:969901
 [1];  [1];  [1];  [1];  [2];  [1];  [3];  [1]
  1. Univ. of California, San Diego, CA (United States)
  2. Univ. of California, San Diego, CA (United States); Univ. of Iceland, Reykjavik (Iceland)
  3. Virginia Commonwealth Univ., Richmond, VA (United States)

Under EMSL User Proposal 25660, the authors reported that bacterial genomes are organized by structural and functional elements, including promoters, transcription start and termination sites, open reading frames, regulatory noncoding regions, untranslated regions and transcription units. Here, we iteratively integrate high-throughput, genome-wide measurements of RNA polymerase binding locations and mRNA transcript abundance, 5' sequences and translation into proteins to determine the organizational structure of the Escherichia coli K-12 MG1655 genome. Integration of the organizational elements provides an experimentally annotated transcription unit architecture, including alternative transcription start sites, 5' untranslated region, boundaries and open reading frames of each transcription unit. A total of 4,661 transcription units were identified, representing an increase of >530% over current knowledge. This comprehensive transcription unit architecture allows for the elucidation of condition-specific uses of alternative sigma factors at the genome scale. Furthermore, the transcription unit architecture provides a foundation on which to construct genome-scale transcriptional and translational regulatory networks.

Research Organization:
Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
969901
Journal Information:
Nature Biotechnology, Vol. 27, Issue 11; ISSN 1087-0156
Country of Publication:
United States
Language:
English