Bacterial DNA replication is carefully controlled at the initiation stage, including by regulation of the essential activity of DnaA protein. The cellular membrane has long been hypothesized to be involved in chromosomal replication, with accumulating evidence indicating membranes have a profound influence on DnaA protein. DnaA protein is found at the cell membrane in vivo, and membrane liposomes containing acidic phospholipids can reactivate an inert form of DnaA protein into replicatively active DnaA in vitro, with a distinct region of DnaA protein found inserted into the hydrophobic interior of the membrane bilayer. Conversely, the membrane-associated protein, Hda participates in converting active DnaA into its inactive form commensurate with DNA replication. Certain mutant forms of DnaA protein are able to suppress the arrested growth of cells that lack an adequate level of acidic phospholipids, further implicating a close link between chromosomal replication and the cell membrane. The long-term goal of this research is to elucidate the physiological significance of the influence of membranes on chromosomal replication. The research outlined here uses biochemical approaches with defined components, physiological studies, cytolocalization techniques, and structural studies to directly test the hypothesis that the cellular membrane participates in the regulation of DnaA protein activity.
The Specific Aims are to: 1. Analyze how an inadequate level of acidic phospholipids affects the cell-cycle, and identify the molecular mechanism of how DnaA(L366K) suppresses the growth-arrest of acidic phospholipid-deficient cells. Determine whether cells are arrested at a specific point or randomly in the cell-cycle as they are depleted of acidic phospholipids. Identify the properties or functions of DnaA(L366K), distinct from wild-type DnaA, that allow continued growth in cells lacking sufficient amounts of acidic phospholipids. 2. Determine if acidic phospholipids participate in the cell-cycle localization of DnaA and the chromosomal origin, and the membrane association of Hda protein. Using fluorescence microscopy of living cells, examine the importance of acidic phospholipids in the proper localization of DnaA, the chromosomal origin, and the DnaA-regulating factor, Hda, as cells progress through the cell-cycle. 3. Define the structure of DnaA protein bound to acidic lipid bilayers. Use the lipidic cubic phase in meso method to obtain diffraction-quality crystals for high-resolution structural determination of DnaA protein associated with a lipid bilayer that contains acidic phospholipids. This work should provide insight into the interactions between membrane lipids and DNA synthesis components, and the functions that membranes may play in cell-cycle and growth controlled initiation of chromosomal replication. Furthermore, advances in understanding of how membrane lipids influence DnaA may help direct future investigations in the emerging field of phospholipid-mediated regulation of enzymatic activities. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM049700-11A1S1
Application #
7278849
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Dearolf, Charles R
Project Start
1994-07-01
Project End
2010-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
11
Fiscal Year
2006
Total Cost
$48,412
Indirect Cost
Name
Georgetown University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Saxena, Rahul; Vasudevan, Sona; Patil, Digvijay et al. (2015) Nucleotide-Induced Conformational Changes in Escherichia coli DnaA Protein Are Required for Bacterial ORC to Pre-RC Conversion at the Chromosomal Origin. Int J Mol Sci 16:27897-911
Saxena, Rahul; Fingland, Nicholas; Patil, Digvijay et al. (2013) Crosstalk between DnaA protein, the initiator of Escherichia coli chromosomal replication, and acidic phospholipids present in bacterial membranes. Int J Mol Sci 14:8517-37
Fingland, Nicholas; Flatten, Ingvild; Downey, Christopher D et al. (2012) Depletion of acidic phospholipids influences chromosomal replication in Escherichia coli. Microbiologyopen 1:450-66
Saxena, Rahul; Rozgaja, Tania; Grimwade, Julia et al. (2011) Remodeling of nucleoprotein complexes is independent of the nucleotide state of a mutant AAA+ protein. J Biol Chem 286:33770-7
Downey, Christopher D; Crooke, Elliott; McHenry, Charles S (2011) Polymerase chaperoning and multiple ATPase sites enable the E. coli DNA polymerase III holoenzyme to rapidly form initiation complexes. J Mol Biol 412:340-53
Boeneman, Kelly; Fossum, Solveig; Yang, Yanhua et al. (2009) Escherichia coli DnaA forms helical structures along the longitudinal cell axis distinct from MreB filaments. Mol Microbiol 72:645-57
Fossum, Solveig; Crooke, Elliott; Skarstad, Kirsten (2007) Organization of sister origins and replisomes during multifork DNA replication in Escherichia coli. EMBO J 26:4514-22
Camara, Johanna E; Breier, Adam M; Brendler, Therese et al. (2005) Hda inactivation of DnaA is the predominant mechanism preventing hyperinitiation of Escherichia coli DNA replication. EMBO Rep 6:736-41
Li, Zhenya; Kitchen, Jennifer L; Boeneman, Kelly et al. (2005) Restoration of growth to acidic phospholipid-deficient cells by DnaA(L366K) is independent of its capacity for nucleotide binding and exchange and requires DnaA. J Biol Chem 280:9796-801
Camara, Johanna Eltz; Skarstad, Kirsten; Crooke, Elliott (2003) Controlled initiation of chromosomal replication in Escherichia coli requires functional Hda protein. J Bacteriol 185:3244-8

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