Melanocortin-3 receptor deficient cells, non-human...

Multicellular living organisms and unmodified parts thereof and – Nonhuman animal – Transgenic nonhuman animal

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S325000, C435S352000, C435S354000

Reexamination Certificate

active

07321074

ABSTRACT:
Cells and non-human transgenic animals have been engineered to be deficient in the gene encoding the melcanocortin-3 receptor protein (MC-3R). MC-3R deficient transgenic animals have increased fatmass and reduced lean body mass, showing that the MC-3R protein is involved in the regulation of body fat and muscle mass. These MC-3R deficient transgenic animals can be used to select for and test potential modulators of MC-3R. This data allows for methods of screening for MC-3R modulators which effect body weight and associated methods of treating various disorders associated with inappropriate regulation of body weight. The disclosure also relates to a MC-3R/MC-4R double knockout mouse which can be used to select for and test potential modulators (e.g., agonists or antagonists) of MC-3R and/or MC-4R. It is shown that MC-3R serves a non-redundant role, when compared to MC-4R, in the regulation of energy homeostasis.

REFERENCES:
patent: 5622860 (1997-04-01), Yamada et al.
patent: 5703220 (1997-12-01), Yamada et al.
patent: 5837521 (1998-11-01), Cone et al.
patent: 5908609 (1999-06-01), Lee et al.
patent: 5932779 (1999-08-01), Lee et al.
patent: WO 02/03793 (2002-01-01), None
Desarnaud et al. (1994) Molecular cloning, functional expression and pharmacological characterization of a mouse melanocortin receptor gene. Biochem. J. 299: 367-373.
Bradley et al. (1992) Modifying the mouse: Design and desire. Bio/Technology 10: 534-539.
Campbell and Wilmut (1997) Totipotency or multipotentiality of cultured cells: Applications and progress. Theriogenology 47: 63-72.
Donehower et al. (1995) Effects of genetic background on tumorigenesis in p53-deficient mice. Molecular Carcinogenesis 14: 16-22.
Jacks et al. (1992) Effects of an Rb mutation in the mouse. Nature 359: 295-300.
Jaenisch et al. (1988) Transgenic Animals. Science 240: 1468-1474.
Kuehn et al. (1987) A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice. Nature 326: 295-298.
Moens et al. (1993) Defects in heart and lung Development in compound heterozygotes for two different targeted mutations at the N-myc locus. Development 119: 485-499.
Mullins et al. (1996) Transgenesis in the rat and larger mammals. J. Clin. Invest. 97(7): 1557-1560.
Sigmund, CD (2000) Viewpoint: Are studies in genetically altered mice out of control? Arterioscler. Thromb. Vasc. Biol. 20: 1425-1429.
Bert, C., et al., Molecular and Cellular Endocrinology, “Production of recombinant rat proopiomelanocortin 1-74 and characterization of its mitogenic action on pituitary lactotrophs”, vol. 154, pp. 111-122, 1999.
Boston, Bruce A., et al., Science, “Independent and additive effects of central POMC and leptin pathways on murine obesity”, vol. 278, pp. 1641-1644, 1997.
Butler, Andrew A., et al., Endocrinology, “A unique metabolic syndrome causes obesity in the melanocortin-3 receptor-deficient mouse”, vol. 141, No. 9, pp. 3518-3521, 2000.
Capecchi, Mario R., et al., Trends in Genetics, “The new mouse genetics: altering the genome by gene targeting”, vol. 5, No. 3, pp. 70-76, 1989.
Chen, Wenbiao, et al., Analytical Biochemistry, “A colorimetric assay for measuring activation of G - and G - Coupled Signaling Pathways”, vol. 226, pp. 349-354, 1995.
Chen, Wenbiao, et al., Cell, “Exocrine gland dysfunction in MC5-R-deficient mice: evidence for coordinated regulation of exocrine gland function by melanocortin peptides”, vol. 91, pp. 789-798, 1997.
Chen, Peilin, et al., Endocrinology, “Altered expression of agouti-related protein and its colocalization with neuropeptide Y in the arcuate nucleus of the hypothalamus during lactation”, vol. 140, No. 6, 1999.
Cunningham, Matthew J., et al., Biology of Reproduction, “Leptin's actions on the reproductive axis: perspectives and mechanisms”, vol. 60, pp. 216-222, 1999.
Chen, Airu S., et al, Nature Genetics, “Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass”, vol. 26, pp. 97-102, 2000.
Cone, Roger D., et al., Recent Progress in Hormone Research, “The melanocortin receptors: agonists, antagonists, and the hormonal control of pigmentation”, vol. 51, pp. 287-318, 1996.
Dinulescu, Daniela M., et al., Proc. Natl. Acad. Sci., “Mahogany (mg)stimulates feeding and increases basal metabolic rate independent of its supression of agouti”, vol. 95, pp. 12707-12712, 1998.
Elias, Carole F., et al., Neuron, “Leptin activates hypothalamic CART neurons projecting to the spinal cord”, vol. 21, pp. 1375-1385, 1998.
Fan, Wei, et al., Letters to Nature, “Role of melanocortinergic neurons in feeding and the agouti obesity syndrome”, vol. 385, pp. 165-168, 1997.
Finn, Patricia D., et al., Endocrinology, “The stimulatory effect of leptin on the neuroedocrine reproductive axis of the monkey”, vol. 139, pp. 4652-4662, 1998.
Fong, Tung Ming, et al., Biochemical and Biophysical Research Communications, “ART (Protein product of agouti-related transcript) as an antagonist of MC-3 and MC-4 receptors”, vol. 237, pp. 629-631, 1997.
Gantz, Ira, et al., The Journal of Biological Chemistry, “Molecular cloning of a novel melanocortin receptor”, vol. 268, Nol. 11, pp. 8246-8250, 1993.
Giros, Bruno, et al., Nature, “Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter”, vol. 379, pp. 606-612, 1996.
Guan, Xio-Ming, et al., Molecular Brain Research 59, “Evidence of altered hypothalamic pro-opiomelanocortin
europeptide Y mRNA expression in tubby mice”, vol. 59, pp. 273-279, 1998.
Gunn, Teresa M., et al., Letters to Nature, “The mousemahoganylocus encodes a transmembrane form of human attractin”, vol. 398, pp. 152-156, 1999.
Hadley, Mac E., et al., Pharmaceutical Biotechnology, “Discovery and development of novel melanogenic drugs”, pp. 575-595, 1998.
Hahn,Tina M., et al, Nature Neuroscience, “Coexpression of Agrp and NPY in fasting-activated hypothalamic neurons”, vol. 1, No. 4, pp. 271-272, 1998.
Haynes, William G., et al., Hypertension, “Interactions Between the melanocortin system and leptin in control of sympathetic nerve traffic”, vol. 33, pp. 542-547, 1999.
Huszar, Dennis et al., Cell, “Targeted disruption of the melanocortin-4 receptor results in obesity in mice”, vol. 88, pp. 131-11, 1997.
Kalra, Satya P., et al., Endocrine Reviews, “Interacting appetite-regulating pathways in the hypothalamic regulation of body weight”, vol. 20, No. 1, pp. 68-100, 1999.
Kask, Ants, et al., Endocrinology, “Discovery of a novel superpotent and selective melanocortin-4 receptor antagonist (HS024): evaluation in Vitro and in Vivo”, vol. 139, No. 12, 1998.
Life Science Dictionary, Hemizygous Definition, 2002.
Lu, Dongsi, et al., Letters to Nature, “Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor”, vol. 371, pp. 799-802, 1994.
Marsh, Donald J., et al., Nature Genetics, “Responsse of melanocortin-4-deficient mice to anorectic and orexigenic peptides”, vol. 21, pp. 119-122, 1999.
Miltenberger, Rosalynn J., et al., J. Nutr., “The role of the agouti gene in the yellow obese syndrome”, vol. 127, pp. 1902S-1907S, 1997.
Mountjoy, Kathleen G., et al., Molecular Endocrinology, “Localization of the melanocortin-4 receptor (MC4-R) in neuroendocrine and autonmic control circuits in the brain”, vol. 8, pp. 1298-1308, 1994.
Mountjoy, Kathleen G., et al., Molecular and Cellular Endocrinology, “Obesity, diabetes and functions for proopiomelanocortin-derived peptides”, vol. 128, pp. 171-177, 1997.
Nagle, Deborah L., et al., Letters to Nature, “Themahoganyprotein is a receptor involved in suppression of obesity”, vol. 398, pp. 148-152, 1999.
Roselli-Rehfuss, Linda, et al., Proc. Natl. Acad. Sci., “

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Melanocortin-3 receptor deficient cells, non-human... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Melanocortin-3 receptor deficient cells, non-human..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Melanocortin-3 receptor deficient cells, non-human... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2782870

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.