Peter C. Angeletti, PhD

Assistant Professor Nebraska Center for Virology School of Biological Sciences University of Nebraska - Lincoln E128 Beadle Center Lincoln, NE 68588-0666 Phone: 402-472-3986 Fax: 402-472-8722 E-mail: pangeletti2@unl.edu

Please visit our Lab Webpage: http://ncv.unl.edu/Angeletti/Angeletti.html

Research Interests:

My research is focused on DNA replication and maintenance of Human papillomaviruses (HPVs) which infect the stratified epithelium of the genital tract. There are currently 20 million Americans infected with genital HPVs with 5.5 million new infections reported each year. While all genital HPVs possess the ability to induce benign warts, the “high-risk” HPVs (Types 16, 18, and 31 for example) are associated with an increased likelihood for progression of lesions to malignant cancer.

In their normal life cycle, HPVs exist as low-copy nuclear plasmids in the host basal epithelium where they can be maintained indefinitely. The viral life cycle is tightly linked to the differentiation program of the stratified epithelium, such that viral genome amplification only occurs in differentiated cells. Viral trans-acting factors, E1 and E2, play an important role in replication; E1, a helicase, recruits polymerase alpha to the origin of replication, while E2 acts cooperatively by binding and recruiting E1 to the origin of replication. E2 functions in two other important ways; by inducing transcription of viral genes, and by improving the inheritance of newly synthesized viral genomes to daughter cells. It is thought that E2 performs this function by tethering viral genomes to mitotic chromosomes, thus allowing accurate partitioning.

A major area of interest for my lab is the study of cis and trans-acting signals that control replication and maintenance of HPV genomes. We are currently investigating the role of E1 and E2 proteins in long-term replication during the viral lifecycle. We are also interested in determining the extent to which cellular factors influence stable replication of HPVs through the long control region (LCR).

In order to approach these studies, in addition to standard human cell culture, we are using a novel yeast-based system, which allows stable episomal replication of full-length HPV genomes (Angeletti et al. 2002 and Kim et al. 2005).

Figure 1: Autonomous replication of HPV16 in yeast.

The yeast/HPV system is powerful since it allows modeling of several HPV functions, including replication, transcription, and encapsidation. It provides a convenient means to assess the cis and trans-acting functions required for replication HPVs, as well as superior yeast genetic tools to determine the involvement of cellular genes in various viral functions.

Figure 2: Encapsidation of full-length HPV16 in yeast. HPV virions produced in yeast have the characteristic morphology and size of authentic HPV particles.

Using this system we are also currently investigating the physical parameters of HPV encapsidation (Angeletti, Methods in Molecular Medicine, 2005). Specifically, we are interested in how the viral factors E2 and L2 function in virion assembly and how they effect infectivity.

Another emerging interest of the lab is the investigation of HPV strains found in HIV positive patients in the sub-Saharan country of Zambia. In these studies we are investigating the prevalence of high-risk HPVs in Zambian patients and how HIV status and CD4 counts influence HPV-related disease; genital warts and dysplasias.

Selected Publications:

1. Angeletti, P. C. A yeast model system for human papillomaviruses. Human Papillomaviruses: Methods and Protocols, Methods in Molecular Medicine. Editor Doorbar, J., Humana Press, Totowa, NJ. (in press).

2. Vaeteewoottacharn, K., Chamutpong, S. Ponglikitmongkol, M. and Angeletti P. C. Differential localization of HPV16 E6 splice products with E6-associated protein Virology Journal 2: 50 (2005).

3. Kim, K., Angeletti, P. C., Hassebroek, E. C. and Lambert, P. F. Identification of Cis-acting Elements that Mediate the Replication andMaintenance of Human Papillomavirus type 16 Genomes in Saccharomyces cerevisiae. Journal of Virology 79, 5933-5942 (2005).

4. Joung, I., Angeletti P. C. and Engler, J. A. Functional implications in apoptosis by interferon inducible gene product 1-8D, the binding protein to adenovirus preterminal protein The Journal of Microbiology, 41, 295-299. (2003).

5. Angeletti, P. C., Kim, K., Fernandes, F. J. and Lambert, P. F. Stable replication of papillomavirus genomes in Saccharomyces cerevisiae. Journal of Virology 76, 3350-3358 (2002).

6. Angeletti, P. C., Walker, D., and Panganiban, A. T. Small glutamine-rich protein/Viral protein U-binding protein is a novel co-chaperone that affects Hsp70 activity. Cell Stress and Chaperones 7, 258-268 (2002).

7. Angeletti, P. C. and Engler, J. A. Adenovirus preterminal protein binds to the CAD enzyme at active sites of viral replication on the nuclear matrix. Journal of Virology 72, 2896-2904 (1998).

8. Sanchez, V., Angeletti, P. C., Engler, J. A., and Britt, W. J.
   Localization of human cytomegalovirus structural proteins to the nuclear matrix of infected human fibroblasts. Journal of Virology 72, 3321-3329 (1998).

9. Angeletti, P. C., and Engler, J. A. Tyrosine kinase-dependent release of an Adenovirus preterminal protein complex from the nuclear matrix. Journal of Virology 70, 3060-3067 (1996).

10. Lucher, L. A., Kuntirat, B., Chowrira, B., Zhao, J., and Angeletti, P. C. Altered synthesis of adenovirus 12 DNA-binding protein but not DNA polymerase during abortive infection of hamster cells. Virology 189, 187-195 (1992).

Selected Abstracts:

1. Encapsidation of human papillomavirus geneomes in Saccharomyces cerevisiae.Molecular Biology of DNA Tumor Viruses Conference. (Madison, Wisconsin), July, 2004.

2. Angeletti, P. C., Kim, K., Fernandes, F. J. and Lambert, P. F. Replication and encapsidation of human papillomavirus genomes in Saccharomyces cerevisiae. The DNA Tumor Virus Meeting. (Trieste, Italy), July 2003.

3. Angeletti, P. C., Kim, K., Fernandes, F. J. and Lambert, P. F. Biological functions of the HPV16 genome in Saccharomyces cerevisiae. International Papillomavirus Conference, Pasteur Institute. (Paris, France), Oct., 2002.

4. Angeletti, P. C., Kim, K., Fernandes, F. J. and Lambert, P. F. Biological functions of the HPV16 genome in Saccharomyces cerevisiae. Molecular Biology of DNA Tumor Viruses Conference. (Madison, Wisconsin), July, 2002.

5. Angeletti, P. C., Kim, K., Grdzelishvilli, V. Z., Ahlquist, P. and Lambert, P. F. Stable replication of Papillomaviruses in Saccharomyces cerevisiae. International Papillomavirus Conference. (Florianopolis, Brazil), Sept., 2001.

6. Angeletti, P. C. and Lambert, P. F. Spontaneous loss of BPV-1 DNA from zelda cells. International Papillomavirus Conference. (Barcelona, Spain), July, 2000.

7. Angeletti, P. C. and Engler, J. A. Interferon inducible gene product 1-8d disrupts Adenovirus preterminal protein foci on the nuclear matrix Small DNA Tumor Virus Meeting (Madison, Wisconsin), May, 1998.

8. Angeletti, P. C. and Engler, J. A. Tyrosine kinase-dependent release of an Adenovirus preterminal protein complex from the nuclear matrix. Keystone Symposium on Viral Genome Replication, (Durango, Colorado) March, 1996.

9. Angeletti, P. C., and Engler, J. A. Adenovirus pTP associates with a nuclear matrix component, and the complex can be solubilized by phosphorylation. Keystone Symposium on the Nuclear Matrix, April 1995. Journal of Cellular Biochemistry vol 21B, (Hilton Head, South Carolina).

10. Angeletti, P. C., and Engler, J. A. Interactions of Adenovirus pTP with nuclear matrix proteins. American Society for Virology Annual Meeting 1994. (Madison, Wisconsin).