Gene encoding a new TRP channel is mutated in mucolipidosis IV

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S069100, C435S252300, C435S320100, C536S023500, C536S024310

Reexamination Certificate

active

07041448

ABSTRACT:
The present invention relates to identification of a gene that is inactivated in a mucolipidosis condition. In particular, the invention concerns mutations that disrupt a mucolipin, preferably MCOLN1, in mucolipidosis IV. Recombinant nucleic acids encoding mutant forms of MCOLN1, oligonucleotides specific for such mutations, and diagnostic and therapeutic applications related to these discoveries, are also contemplated.

REFERENCES:
patent: 6300096 (2001-10-01), Stahl et al.
patent: 2002/0035056 (2002-03-01), Curtis et al.
patent: 2002/0182671 (2002-12-01), Lal et al.
patent: WO-WO 01/77331 (2001-10-01), None
Sun et al. “Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel.” Human Molecular Genetics vol. 9(17):2471-2478, Sep. 2000.
Bargal et al. “Identification of the gene causing mucolipidosis type IV.” Nature Genetics vol. 26:120-123, Sep. 2000.
Bassi et al. “Cloning of the gene encoding a novel integral membrane protein, Mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IV.” American Journal of Human Genetics vol. 67:1110-1120, 2000.
“From Worm To Man: Three Subfamilies of TRP Channels”, Christian Harteneck et al., Trends Neurosci., vol. 23, No. 4, 2000, Elsevier Science Ltd., 2000.
“Compromised Cytoarchitecture and Polarized Trafficking in Autosomal Dominant Polycystic Kidney Disease Cells”, Audra J. Charron et al., The Journal of Cell Biology, vol. 149, No. 1, Apr. 3, 2000, The Rockefeller University Press.
“Cellular and Subcellular Distribution of Polycystin-2, the Protein Product of the PKD2 Gene”, Lukas Foggensteiner et al., Journal of the American Society of Nephrology, 2000.
“Ion Channels and Synaptic Organization: Analysis of the Drosophila Genome”, J. Troy Littleton et al., Neuron, vol. 26, 35-43, Apr. 2000, Cell Press 2000.
“Mucolipidosis IV Consists of One Complementation Group”, EHUD Goldin et al., Proc. Natl. Acad. Sci., USA, vol. 96, pp. 8562-8566, Jul. 1999, Genetics.
“Mapping of the Mucolipidosis Type IV Gene to Chromosome 19p and Definition of Founder Haplotypes.”, Susan A. Slaugenhaupt et al., The American Society of Human Genetics, 1999.
“Mucolipidosis Type IV Characteristic MRI Findings”, Dr. K.P. Frei et al., American Academy of Neurology, 1998.
“Abnormal Transport Along the Lysosomal Pathway in Mucolipidosis, Type IV Disease”, Chii-Shiarng Chen et al., Proc. Natl. Acad. Sci., USA, vol. 95, pp 6373-6378, May 1998, Medical Sciences.
“Constitutive Achlorhydria in Mucolipidosis Type IV”, Raphael Schiffmann et al., Proc. Natl. Acad. Sci., USA, vol. 95, pp 1207-1212, Feb. 1998, Medical Sciences.
“Recommendations for a Nomenclature System for Human Gen Mutations”, Dr. Stylianos E. Antonarakis et al., Human Mutation 11:1-3 (1998), Wiley-Liss, Inc. 1998.
“Cultured Skin Fibroblasts Derived From Patients With Mucolipidosis 4 Are Auto-Fluorescent”, Ehud Goldin et al., Pediatric Research, vol. 37, No. 6, 1995, International Pediatric Research Foundation, Inc. 1995.
“The Effect of Lysosomal Storage Diseases on Secretory Cells: An Ultrastructural Study of Pancreas as an Example”, I. Hammel et al.; J. Submicrosc. Cytol., Pathology, 27 (2), 143-160, 1995.
“‘G’ to ‘A’ Mutation at Position -1 of a 5′ Splice Site in a Late Infantile Form of Tay-Sachs Disease”, Said Akli et al., The Journal of Biological Chemistry, vol. 265, No. 13, Issue of May 5, pp. 7324-7330, 1990, The American Society For Biochemistry and Molecular Biology, Inc. 1990.

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

Gene encoding a new TRP channel is mutated in mucolipidosis IV does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Gene encoding a new TRP channel is mutated in mucolipidosis IV, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Gene encoding a new TRP channel is mutated in mucolipidosis IV will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3643507

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