Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Recombinant dna technique included in method of making a...
Reexamination Certificate
1998-04-21
2001-06-05
Carlson, Karen Cochrane (Department: 1653)
Chemistry: molecular biology and microbiology
Micro-organism, tissue cell culture or enzyme using process...
Recombinant dna technique included in method of making a...
C435S006120, C435S091200, C435S252300, C435S320100, C536S023100
Reexamination Certificate
active
06242214
ABSTRACT:
FIELD OF THE INVENTION
This invention relates to nucleic acid and amino acid sequences of human GTPase-associated proteins and to the use of these sequences in the diagnosis, treatment, and prevention of cell proliferation disorders, autoimmune/inflammatory disorders, and vesicle trafficking disorders.
BACKGROUND OF THE INVENTION
The GTPase superfamily includes many proteins which act as intracellular switches in signal transduction and vesicle trafficking. (Lodish, H. et al. (1995)
Molecular Cell Biology
, Scientific American Books, Inc., New York, N.Y., pp. 876-877.) The family includes both heterotrimeric GTPases (G proteins) and low molecular weight GTPases related to Ras. In both cases the GTPase activity is regulated through interactions with other proteins.
The heterotrimeric G proteins, a family of peripheral membrane GTPases, are present in all cells. They control metabolic, humoral, neural, and developmental functions by transducing hormonal, neurotransmitter, and sensory signals into an array of cellular responses. Each G protein is composed of an alpha (&agr;), a beta (&bgr;), and a gamma (&ggr;) subunit, associated as a complex in an inactive GDP-bound form. G
&agr;
binds GDP or GTP and contains the GTPase activity. The &bgr;&ggr; complex enhances binding of G
&agr;
to a receptor. G
&ggr;
is necessary for the folding and activity of G
&bgr;
. (Neer, E. J. et al. (1994) Nature 371:297-300.) Multiple homologs of each subunit have been identified in mammalian tissues, and different combinations of subunits have specific functions and tissue specificities. (Spiegel, A. M. (1997) J. Inher. Metab. Dis. 20:113-121.)
G protein activity is triggered by seven-transmembrane cell surface receptors (G protein coupled receptors; GPCRs) which respond to lipid analogs, amino acids and their derivatives, peptides, cytokines, and specialized stimuli such as light, taste, and odor. Activation of the receptor by its stimulus causes the replacement of the G protein-bound GDP with GTP. G
&agr;
-GTP dissociates from the receptor and the &bgr;&ggr; complex. Both G
&agr;
-GTP and the &bgr;&ggr; complex stimulate or inhibit effector molecules to transmit the signal delivered to the GPCR. The signaling is stopped when G
&agr;
hydrolyzes its bound GTP to GDP and reassociates with the &bgr;&ggr; complex. G
&agr;
interacts with the effectors adenylate cyclase, ion channels, and phospholipase C-&bgr;, and the &bgr;&ggr; complex interacts with adenylate cyclase, phospholipase C-&bgr;, &bgr;-adrenergic receptor kinase, phosducin, phosphoinositide 3-kinase, and potassium channels. In yeast, the &bgr;&ggr; complex mediates a G protein dependent mating response. (Müller, S. et al. (1996) J. Biol. Chem. 271:11781-11786; Meij, J. T. A. (1996) Mol. Cell. Biochem. 157:31-38; and Watson, A. J. et al. (1994) J. Biol. Chem. 269:22150-22156.)
G
&bgr;
proteins, also known as &bgr; transducins, are all about 340 amino acids in length and contain seven tandem repeats of the WD-repeat sequence motif, a motif found in many proteins with regulatory functions. WD-repeat proteins contain from four to eight copies of a loosely conserved repeat of approximately 40 amino acids. Each repeat contains a central conserved region bracketed by Gly-His and Trp-Asp (WD) residues. The three-dimensional structure of the &bgr;&ggr; complex has been solved, and G
&bgr;
was shown to fold into a circular seven-bladed &bgr; propeller. Other WD-repeat proteins are likely to form similar &bgr; propeller structures. (Neer, supra; and Garcia-Higuera, I. et al. (1996) Biochemistry 35:13985-13994.)
Other proteins with seven WD repeats have been found, some of which have roles in signal transduction. Mutations in LIS1, a subunit of the human platelet activating factor acetylhydrolase, cause Miller-Dieker lissencephaly, a severe brain malformation. MSI1 is a negative regulator of Ras-mediated cAMP increase in yeast. RACK1 binds activated protein kinase C, and RbAp48 binds retinoblastoma protein. CstF is required for polyadenylation of mammalian pre-mRNA in vitro and associates with subunits of cleavage-stimulating factor. &bgr;Trcp is a yeast protein whose expression suppresses mutations in CDC15, a gene needed for normal anaphase in yeast. Uncharacterized 7 WD-repeat proteins exist as well. (Neer, supra.)
Research indicates that an irregularity in any GPCR pathway component can cause a physiological defect. (Meij, supra.) For example, mutations in the components of the cell signaling cascade as well as alterations in the expression pattern of these components may result in abnormal activation of leukocytes and lymphocytes, leading to the tissue damage and destruction seen in autoimmune diseases such as rheumatoid arthritis, biliary cirrhosis, hemolytic anemia, lupus erythematosus, and thyroiditis. T cell activation is a G protein regulated process. (Aussel, C. et al. (1988) J. Immunol. 140:215-220.)
Irregularities in G protein signaling also have a role in abnormal cell proliferation. Cyclic AMP stimulation of brain, thyroid, adrenal, and gonadal tissue proliferation is regulated by G proteins. Mutations in G&bgr; subunits have been found in growth-hormone-secreting pituitary somatotroph tumors, hyperfunctioning thyroid adenomas, and ovarian and adrenal neoplasms. (Spiegel, supra.)
Other genetic disorders caused by loss or gain of function mutations in G
&agr;
subunits include Albright hereditary osteodystrophy, pseudohypoparathyroidism type Ia with precocious puberty, McCune-Albright syndrome, and congenital night blindness. (Spiegel, supra.) GPCR mutations are responsible for many diseases including color blindness, retinitis pigmentosa, congenital night blindness, nephrogenic diabetes insipidus, familial adrenocorticotropic hormone (ACTH) resistance, hypergonadotropic ovarian dysgenesis, familial male precocious puberty, male pseudohermaphroditism, sporadic hyperfunctional thyroid nodules, familial nonautoimmune hyperthyroidism, familial hypothyroidism, familial hypocalciuric hypercalcemia
eonatal severe primary hyperparathyroidism, familial hypoparathyroidism, congenital bleeding, Hirschsprung disease, Jansen metaphyseal chondrodysplasia, and familial growth hormone deficiency. (Spiegel, supra.) A G-protein controlled pathway, the &bgr;-adrenoreceptor/adenylate cyclase pathway, appears to be desensitized in heart failure. (Meij, supra.)
Rab proteins, which are Ras-related low molecular weight GTPases, regulate vesicular transport between subcellular compartments of eukaryotic cells. During this process, vesicles bud from a donor membrane and fuse with a recipient to deliver internalized materials. Rab proteins assist the binding of transport vesicles to their accepter organelles and initiate the vesicle fusion process using the energy from GTP hydrolysis. More than 30 Rab proteins have been identified in a variety of species, and each has a characteristic intracellular location and distinct transport function. Rab5 is localized to endosomes and regulates the fusion of early endosomes into late endosomes. Rab5 function in vesicular transport requires the cooperation of other proteins, including Rab-escort proteins, Rab-specific guanine nucleotide dissociation inhibitor, and rabaptins. (Vitale, G. et al. (1995) Cold Spring Harbor Symp. Quant. Biol. 60:211-220; and Vitale, G. et al. (1998) EMBO J. 17:1941-1951.) Several putative Rab5-interacting proteins expressed in human HeLa cells have been identified using a yeast two-hybrid screen, and their partial nucleotide and amino acids sequences determined. (Vitale (1995) supra.)
Defects in protein trafficking to organelles or the cell surface are involved in numerous human diseases and disorders. Defects in the trafficking of membrane-bound receptors and ion channels are associated with cystic fibrosis (cystic fibrosis transmembrane conductance regulator), glucose-galactose malabsorption syndrome (Na
+
/glucose cotransporter), hypercholesterolemia (low-density lipoprotein receptor), and forms of diabetes mellitus (insulin receptor). Abnormal hormonal secretion is linked to dis
Bandman Olga
Corley Neil C.
Guegler Karl J.
Lal Preeti
Patterson Chandra
Carlson Karen Cochrane
Incyte Pharmaceuticals Inc.
Incyte Pharmaceuticals, Inc.
Srivastava Devesh
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