The long term goal of this research program is to define the role of the Origin Recognition Complex (ORC) in cell cycle progression in eukaryotes. The ORC is a critical component for DMA replication, but also has a role in other cell functions. In particular, we have recently demonstrated that the complex is critically involved in cytokinesis. We found that the smallest ORC subunit, Orc6, is localized to the cell membranes and cleavage furrows of dividing cells. Orc6 interacts with the septin protein Peanut (Pnut) and is involved in cytokinesis in addition to its replication functions. The following specific aims will be pursued: 1) molecular analysis of Orc6-Pnut interaction. The function of conserved sequence motifs of Orc6 and Pnut proteins will be defined and the role of Pnut in Orc6 localization will be determined. 2) Determining the motifs and sequences of Orc6 that are important for DNA binding and replication. Critical residues of Orc6 essential for DNA binding and replication will be identified and their importance confirmed both in vitro and in vivo. 3) Analysis of the intracellular localization of Orc6 during the cell cycle. Functional significance of Orc6 localization during different stages of the cell cycle will be studied. 4) Targeted mutagenesis of Orc6 in vivo and analysis of the loss of function phenotype. Targeted mutagenesis will be used as well as other methods that allow us to mimic the mutant phenotype to study Orc6 functions in vivo. Working with Drosophila will be advantageous for these studies as it allows the use of both biochemical and genetic methods and also permits insights into the developmental as well as tissue specific aspects of replication control. An understanding of the molecular events involved in the initiation of replication and cytokinesis will provide a basis for ultimately controlling these processes. Such control might lead to rationally designed therapies for cancer and may provide the means for regenerating cells lost due to aging, disease or injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM069681-05S1
Application #
7935860
Study Section
Molecular Genetics C Study Section (MGC)
Program Officer
Shapiro, Bert I
Project Start
2009-09-30
Project End
2012-02-28
Budget Start
2009-09-30
Budget End
2012-02-28
Support Year
5
Fiscal Year
2009
Total Cost
$394,602
Indirect Cost
Name
University of Alabama Birmingham
Department
Biochemistry
Type
Schools of Medicine
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Liu, Shixuan; Balasov, Maxim; Wang, Hongfei et al. (2011) Structural analysis of human Orc6 protein reveals a homology with transcription factor TFIIB. Proc Natl Acad Sci U S A 108:7373-8
Svitin, Anton; Chesnokov, Igor (2010) Study of DNA replication in Drosophila using cell free in vitro system. Cell Cycle 9:815-9
Balasov, Maxim; Huijbregts, Richard P H; Chesnokov, Igor (2009) Functional analysis of an Orc6 mutant in Drosophila. Proc Natl Acad Sci U S A 106:10672-7
Duncker, Bernard P; Chesnokov, Igor N; McConkey, Brendan J (2009) The origin recognition complex protein family. Genome Biol 10:214
Huijbregts, Richard P H; Svitin, Anton; Stinnett, Monica W et al. (2009) Drosophila Orc6 facilitates GTPase activity and filament formation of the septin complex. Mol Biol Cell 20:270-81
Balasov, Maxim; Huijbregts, Richard P H; Chesnokov, Igor (2007) Role of the Orc6 protein in origin recognition complex-dependent DNA binding and replication in Drosophila melanogaster. Mol Cell Biol 27:3143-53
Chesnokov, Igor N (2007) Multiple functions of the origin recognition complex. Int Rev Cytol 256:69-109