Multicellular living organisms and unmodified parts thereof and – Nonhuman animal
Reexamination Certificate
2006-05-09
2006-05-09
Crouch, Deborah (Department: 1632)
Multicellular living organisms and unmodified parts thereof and
Nonhuman animal
C800S003000, C800S021000
Reexamination Certificate
active
07041869
ABSTRACT:
The present invention provides a transgenic animal expressing the reporter gene, luciferase, driven by a promoter (e.g. the E2F1 promoter) that acts as a sensor of cell cycle. The luciferase substrate, luciferin, emits light when metabolized, and the light is transmitted through mammalian tissues. Therefore, the transgenic animal model of the present invention allows for monitoring of areas of major cell cycle activity, a characteristic of cancer cells, under adequate visualization conditions. These transgenic animals are useful as in vivo models for testing preventative measures for cancer as well as for testing novel therapeutic modalities.
REFERENCES:
Vooijs et al. “Noninvasive imaging of spontaneous retinoblastoma pathway-dependent tumors in mice.” Cancer Research 62:1862-1867, 2002.
Kappel et al. “Regulating gene expression in transgenic animals.” Current Opinion in Biotechnology 3:548-553, 1992.
Sandal T “Molecular aspects of the mammalian cell cycle and cancer.” The Oncologist 7:73-81, 2002.
Mullins et al. “Transgenesis in nonmurine species.” Hypertension 22:630-633, 1993.
Houdebine LM “Production of pharmaceutical proteins from transgenic animals.” Journal of Biotechnology 34: 269-287, 1994.
Wall RJ “Transgenic livestock progress and prospects for the future” Theriogenology 45:57-68, 1996.
Cameron ER “Recent advances in transgenic technology” Molecular Biotechnology 7:253-265, 1997.
Sigmund CD “Viewpoint: Are studies in genetically altered mice out of control?” Arterioscler Thromb Vasc Biol 20:1425-1429, 2000.
Niemann H “Transgenic farm animals get off the ground.” Transgenic Research 7:73-75, 1998.
Bhaumik et al. “Optical imaging ofRenilla luciferasereporter gene expression in living mice.” PNAS 99(1): 377-382.
Hasan et al. “Long-term, noninvasive imaging of regulated gene expression in liviing mice.” Genesis 29:116-122, 2001.
Steghens et al. (1998)Firefly luciferasehas two nucleotide binding sites:effect of nucleoside monophosphate and CoA on the light-emission spectra. Biochem J. 336:109-113.
Markova et al. (2004) Cloning and Expression of cDNA for a luciferase from Marine Copepod Metridia Ionga. J. Biol. Chem. 279:3212-3217.
Müller, C. et al. Methylation of the Cyclin A1 Promoter Correlates with Gene Silencing in Somatic Cell Lines, While Tissue-Specific Expression of Cyclin A1 Is Methylation Independent:Molecular and Cellular Biology, May 2000, vol. 20, No. 9, pp. 3316-3329.
Dieckmann, A. et al. The EIA Transcriptional Control Region is Efficiently Activated in Proliferating Tissues of Transgenic Mice:Oncogene, 1994, pp. 2227-2233.
Jiang, Z. et al. Retinoblastoma Gene Promoter Directs Transgene Expression Exclusively to the Nervous System:The Journal of Biological Chemistry, Jan. 5, 2001, vol. 276, No. 1, pp. 593-600.
Holmberg, C. et al. E2F-1-Induced p. 53-Independent Apoptosis in Transgenic Mice:Oncogene, 1998, vol. 17, pp. 143-155.
Pierce, A. et al. Increased E2F1 Activity Induces Skin Tumors in Mice Heterozygous and Nullizygous for p. 53:Proc. Natl. Acad. Sci., Jul. 1998, vol. 95, pp. 8858-8863.
Adler Benjamin Aaron
Crouch Deborah
Lieto Louis D.
Sloan-Kettering Institute for Cancer Research
LandOfFree
Transgenic luciferase mouse does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Transgenic luciferase mouse, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Transgenic luciferase mouse will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3562948