Alpha-2B-adrenergic receptor polymorphisms
The present invention includes polymorphisms in nucleic acids encoding the alpha-2B adrenergic receptor and expressed alpha-2B adrenergic receptor molecule. The invention also pertains to methods and molecules for detecting such polymorphisms. The invention further pertains to the use of such molecules and methods in the diagnosis, prognosis, and treatment of diseases such as cardiovascular and central nervous system diseases.
1. A method of establishing an alpha-2B-adrenergic receptor function comprising:
a. obtaining an isolated polynucleotide that encodes said alpha-2B-adrenergic receptor, or a complement thereof, or a fragment thereof, or a complement of said fragment, that includes nucleotides 901 to 909 of SEQ ID NO: 1, or nucleotides 901 to 909 of SEQ ID NO: 2, or their complements;
b. detecting in said isolated polynucleotide the presence or absence of a deletion polymorphism, said deletion polymorphism exclusively consisting of the deletion of nucleotide positions 901 to 909 of SEQ ID NO: 1; and
c. establishing that the agonist-mediated receptor function of decreasing adenylyl cyclase activity of said alpha-2B-adrenergic receptor is reduced if said deletion polymorphism is present as compared to said agonist-mediated receptor function if said deletion polymorphism is absent.
2. A method according to claim 1 , wherein said detecting comprises a hybridization step.
3. A method of phenotyping an individual, comprising:
establishing the alpha-2B-adrenergic receptor function according to claim 1 , thereby determining phenotype of said individual from whom said isolated polynucleotide was obtained.
4. The method according to claim 2 , further comprising amplifying the deletion polymorphism of the polynucleotide prior to the hybridization.
5. The method according to claim 2 , wherein said hybridization is selected from the group consisting of southern blot, dot blot, reverse dot blot, northern blot, and allele-specific oligonucleotide hybridization.
6. The method according to claim 2 , wherein the hybridization includes hybridization of an oligonucleotide to a region of the polynucleotide, the oligonucleotide being labeled with a label selected from the group consisting of radiolabel, fluorescent label, bioluminescent label, chemiluminescent label, nucleic acid label, hapten label, and enzyme label.
7. The method according to claim 2 , wherein said detecting comprises a step selected from the group consisting of dideoxy sequencing, restriction digestion, allele-specific polymerase reaction, single-stranded conformational polymorphism analysis, genetic bit analysis, temperature gradient gel electrophoresis; ligase chain reaction, or ligase/polymerase genetic bit analysis, and random amplification of DNA.
8. The method according to claim 6 , wherein the oligonucleotide is from about 10 to about 50 nucleotides in length.
9. A method of establishing an alpha-2B-adrenergic receptor function comprising:
a. obtaining an isolated polynucleotide that encodes said alpha-2B-adrenergic receptor or a complement thereof, or a fragment thereof, or a complement of said fragment, that includes nucleotides 901 to 909 of SEQ ID NO: 1, or nucleotides 901 to 909 of SEQ ID NO: 2, or their complements;
b. indirectly detecting in said isolated polynucleotide the presence or absence of a deletion polymorphism, said deletion polymorphism exclusively consisting of the deletion of nucleotide positions 901 to 909 of SEQ ID NO: 1; and
c. establishing that the agonist-mediated receptor function of decreasing adenylyl cyclase activity of said alpha-2B-adrenergic receptor is reduced if said deletion polymorphism is present as compared to said agonist-mediated receptor function if said deletion polymorphism is absent.
10. The method of claim 1 , wherein the agonist is selected from a group consisting of epinephrine, norepinephrine, clonidine, oxymetazoline, guanabenz, UK14304, BHT933 and combinations thereof.
11. The method of claim 9 , wherein the agonist is selected from a group consisting of epinephrine, norepinephrine, clonidine, oxymetazoline, guanabenz, UK14304, BHT933 and combinations thereof.