Literature DB >> 15326179

DiaA, a novel DnaA-binding protein, ensures the timely initiation of Escherichia coli chromosome replication.

Takuma Ishida1, Nobuyoshi Akimitsu, Tamami Kashioka, Masakazu Hatano, Toshio Kubota, Yasuyuki Ogata, Kazuhisa Sekimizu, Tsutomu Katayama.   

Abstract

The DnaA protein is the initiator of Escherichia coli chromosomal replication. In this study, we identify a novel DnaA-associating protein, DiaA, that is required for the timely initiation of replication during the cell cycle. DiaA promotes the growth of specific temperature-sensitive dnaA mutants and ensures stable minichromosome maintenance, whereas DiaA does not decrease the cellular DnaA content. A diaA::Tn5 mutation suppresses the cold-sensitive growth of an overinitiation type dnaA mutant independently of SeqA, a negative modulator of initiation. Flow cytometry analyses revealed that the timing of replication initiation is disrupted in the diaA mutant cells as well as wild-type cells with pBR322 expressing the diaA gene. Gel filtration and chemical cross-linking experiments showed that purified DiaA forms a stable homodimer. Immunoblotting analysis indicated that a single cell contains about 280 DiaA dimers. DiaA stimulates minichromosome replication in an in vitro system especially when the level of DnaA included is limited. Moreover, specific and direct binding between DnaA and DiaA was observed, which requires a DnaA N-terminal region. DiaA binds to both ATP- and ADP-bound forms of DnaA with a similar affinity. Thus, we conclude that DiaA is a novel DnaA-associating factor that is crucial to ensure the timely initiation of chromosomal replication.

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Year:  2004        PMID: 15326179     DOI: 10.1074/jbc.M402762200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  52 in total

Review 1.  Regulation of DnaA assembly and activity: taking directions from the genome.

Authors:  Alan C Leonard; Julia E Grimwade
Journal:  Annu Rev Microbiol       Date:  2011       Impact factor: 15.500

Review 2.  Regulating DnaA complex assembly: it is time to fill the gaps.

Authors:  Alan C Leonard; Julia E Grimwade
Journal:  Curr Opin Microbiol       Date:  2010-10-27       Impact factor: 7.934

3.  NMR structure of the N-terminal domain of the replication initiator protein DnaA.

Authors:  Thomas J Lowery; Jeffrey G Pelton; John-Marc Chandonia; Rosalind Kim; Hisao Yokota; David E Wemmer
Journal:  J Struct Funct Genomics       Date:  2007-08-07

4.  Hda monomerization by ADP binding promotes replicase clamp-mediated DnaA-ATP hydrolysis.

Authors:  Masayuki Su'etsugu; Kenta Nakamura; Kenji Keyamura; Yuka Kudo; Tsutomu Katayama
Journal:  J Biol Chem       Date:  2008-10-30       Impact factor: 5.157

5.  DiaA dynamics are coupled with changes in initial origin complexes leading to helicase loading.

Authors:  Kenji Keyamura; Yoshito Abe; Masahiro Higashi; Tadashi Ueda; Tsutomu Katayama
Journal:  J Biol Chem       Date:  2009-07-24       Impact factor: 5.157

6.  A role for nonessential domain II of initiator protein, DnaA, in replication control.

Authors:  Kathryn L Molt; Vincent A Sutera; Kathryn K Moore; Susan T Lovett
Journal:  Genetics       Date:  2009-06-22       Impact factor: 4.562

7.  Modes of overinitiation, dnaA gene expression, and inhibition of cell division in a novel cold-sensitive hda mutant of Escherichia coli.

Authors:  Kazuyuki Fujimitsu; Masayuki Su'etsugu; Yoko Yamaguchi; Kensaku Mazda; Nisi Fu; Hironori Kawakami; Tsutomu Katayama
Journal:  J Bacteriol       Date:  2008-05-23       Impact factor: 3.490

8.  Ordered association of helicase loader proteins with the Bacillus subtilis origin of replication in vivo.

Authors:  Wiep Klaas Smits; Alexi I Goranov; Alan D Grossman
Journal:  Mol Microbiol       Date:  2009-12-04       Impact factor: 3.501

9.  Cryptic protein interactions regulate DNA replication initiation.

Authors:  Lindsay A Matthews; Lyle A Simmons
Journal:  Mol Microbiol       Date:  2018-10-21       Impact factor: 3.501

10.  Large-scale transposon mutagenesis of Photobacterium profundum SS9 reveals new genetic loci important for growth at low temperature and high pressure.

Authors:  Federico M Lauro; Khiem Tran; Alessandro Vezzi; Nicola Vitulo; Giorgio Valle; Douglas H Bartlett
Journal:  J Bacteriol       Date:  2007-12-21       Impact factor: 3.490

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