A developmentally regulated chromosomal origin of replication uses essential transcription elements.
- 15 June 1995
- journal article
- research article
- Published by Cold Spring Harbor Laboratory in Genes & Development
- Vol. 9 (12) , 1543-1557
- https://doi.org/10.1101/gad.9.12.1543
Abstract
Only one of the two chromosomes in the asymmetric Caulobacter predivisional cell initiates replication in the progeny cells. Transcription from a strong promoter within the origin occurs uniquely from the replication-competent chromosome at the stalked pole of the predivisional cell. This regulated promoter has an unusual sequence organization, and transcription from this promoter is essential for regulated (cell type-specific) replication. Our analysis defines a new class of bacterial origins and suggests a coupling between transcription and replication that is consistent with the phylogenetic relationship of Caulobacter to the ancestral mitochondrion.Keywords
This publication has 58 references indexed in Scilit:
- A Caulobacter DNA Methyltransferase that Functions only in the Predivisional CellJournal of Molecular Biology, 1994
- Cell-cycle control of a cloned chromosomal origin of replication from Caulobacter crescentusJournal of Molecular Biology, 1992
- Positional information during Caulobacter cell differentiationCurrent Opinion in Genetics & Development, 1991
- REGULATION OF THE CELL DIVISION CYCLE AND DIFFERENTIATION IN BACTERIAAnnual Review of Microbiology, 1990
- Plasmid and chromosomal DNA replication and partitioning during the Caulobacter crescentus cell cycleJournal of Molecular Biology, 1990
- A model for initiation at origins of DNA replicationCell, 1988
- Transcriptional elements as components of eukaryotic origins of DNA replicationCell, 1988
- Differential expression and positioning of chemotaxis methylation proteins in CaulobacterJournal of Molecular Biology, 1984
- Sequence organization of replication origin of the Escherichia coli K-12 chromosomeJournal of Molecular Biology, 1984
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983