Maintenance of genome stability is extremely important in the cell cycle, with genomic instability being the hallmark of cancer cells. DNA re-replication is one type of genomic instability with replication origins firing multiple times during the same cell cycle. Although several genes that regulate DNA re-replication have been identified, the mechanisms behind them remain to be determined. Moreover, whether DNA re-replication control can be used for cancer therapy is unknown.
The aim of this proposal is to investigate the mechanisms by which Cdk1 prevents DNA re-replication during G2/M phase in both human cancer and normal cells, to screen for small molecules that selectively cause DNA re-replication in cancer cells, and to perform genome-wide studies of DNA re-replication control. This study will be useful not only to understand one facet of how our cells maintain a stable genome, but also to provide us with useful therapeutic targets and potential compounds for the treatment of cancer. Therefore, this proposal is relevant to the mission of NIH/NCI in its pursuit of fundamental knowledge about living systems and supporting research, training, and other programs with respect to the cause, diagnosis, prevention, and treatment of cancer.
The Specific Aims of this proposal are:
Aim 1. Investigate the role of Cdkl in regulating Orel activity to prevent DNA re-replication during G2/M. In particular, we will investigate the role of phosphorylation of Orel by Cdk1 kinases during G2/M and whether Orel is involved in re-replication regulation during G2/M.
Aim 2. Screen for small molecules by a HTS assay to identify small compounds that selectively cause DNA rereplication in cancer cells.
Aim 3. Perform cell-based genome-wide studies of DNA re-replication control via a HTS assay by siRNA transfection to identify new genes that involve in DNA re-replication control. My ultimate career goal is to become an independent researcher in the field of cancer research. To accomplish this, currently I am investigating the mechanisms that cause genome instability in cancer cells and its application for cancer therapy, resulting in the application for this award.

Public Health Relevance

Almost all human tumors display genome instability. The proposed work promises to provide not only an understanding of the mechanisms by which human cells maintain their genome stability, and the application of these mechanisms to selective killing of cancer cells, but also the potential compounds and new targets for cancer therapy.

National Institute of Health (NIH)
National Cancer Institute (NCI)
Research Transition Award (R00)
Project #
Application #
Study Section
Special Emphasis Panel (NSS)
Program Officer
Hildesheim, Jeffrey
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
George Washington University
Schools of Medicine
United States
Zip Code
Hao, Jing; Zhu, Wenge (2015) Maintain Genomic Stability: Multitask of DNA Replication Proteins. Transcr Open Access 3:
Jaramillo-Lambert, Aimee; Hao, Jing; Xiao, Haijie et al. (2013) Acidic nucleoplasmic DNA-binding protein (And-1) controls chromosome congression by regulating the assembly of centromere protein A (CENP-A) at centromeres. J Biol Chem 288:1480-8
Li, Y; Jaramillo-Lambert, A N; Yang, Y et al. (2012) And-1 is required for the stability of histone acetyltransferase Gcn5. Oncogene 31:643-52
Lee, Chrissie Y; Johnson, Ronald L; Wichterman-Kouznetsova, Jennifer et al. (2012) High-throughput screening for genes that prevent excess DNA replication in human cells and for molecules that inhibit them. Methods 57:234-48
Zhu, Wenge; Lee, Chrissie Y; Johnson, Ronald L et al. (2011) An image-based, high-throughput screening assay for molecules that induce excess DNA replication in human cancer cells. Mol Cancer Res 9:294-310
Li, Yongming; Jaramillo-Lambert, Aimee; Hao, Jing et al. (2011) The stability of histone acetyltransferase general control non-derepressible (Gcn) 5 is regulated by Cullin4-RING E3 ubiquitin ligase. J Biol Chem 286:41344-52