Claims for Patent: 6,413,719

Summary for Patent: 6,413,719

Title:	KCNQ2 and KCNQ3-potassium channel genes which are mutated in benign familial neonatal convulsions (BFNC) and other epilepsies
Abstract:	Generalized idiopathic epilepsies (IGE) cause 40% of all seizures and commonly have a genetic basis. One type of IGE is Benign Familial Neonatal Convulsions (BFNC), a dominantly inherited disorder of newborns. A submicroscopic deletion of chromosome 20q13.3 which co-segregates with seizures in a BFNC family has been identified. Characterization of cDNAs spanning the deleted region identified a novel voltage-gated potassium channel, KCNQ2, which belongs to a new KCNQ1-like class of potassium channels. Nine other BFNC probands were shown to have KCNQ2 mutations including three missense mutations, three frameshifts, two nonsense mutations, and one splice site mutation. A second gene, KCNQ3, was found in a separate BFNC family in which the mutation had been localized to chromosome 8. A missense mutation was found in this gene in perfect cosegregation with the BFNC phenotype in this latter family. This demonstrates that defects in potassium channels can cause epilepsy. Furthermore, some members of one of the BFNC families with a mutation in KCNQ2 also exhibited rolandic epilepsy and one individual with juvenile myoclonic epilepsy has a mutation in an alternative exon of KCNQ3.
Inventor(s):	Singh; Nanda A. (Heber City, UT), Leppert; Mark F. (Salt Lake City, UT), Charlier; Carole (Sprimont, BE)
Assignee:	University of Utah Research Foundation (Salt Lake City, UT)
Application Number:	09/177,650
Patent Claims:	1. An isolated nucleic acid encoding a protein consisting of the amino acid sequence of SEQ ID NO:2, SEQ ID NO:7, SEQ ID NO:89, SEQ ID NO:91, or SEQ ID NO:96, or a complement of said isolated nucleic acid. 2. An isolated nucleic acid consisting of nucleotides 128-2743 of SEQ ID NO:1, nucleotides 19-2634 of SEQ ID NO:6, nucleotides 1-2273 of SEQ ID NO:88, nucleotides 202-2811 of SEQ ID NO:90, or nucleotides 128-2917 of SEQ ID NO:95, or a complement of said isolated nucleic acid. 3. An isolated nucleic acid encoding a mutant human KCNQ2 or KCNQ3 polypeptide which causes benign familial neonatal convulsions (BFNC), juvenile myoclonic epilepsy (JME) or rolandic epilepsy, or a complement of said isolated nucleic acid. 4. An isolated nucleic acid according to claim 3 wherein said isolated nucleic acid comprises a mutation which causes BFNC, JME, or rolandic epilepsy wherein said mutation is selected from the group consisting of: a G at nucleotide 978 of SEQ ID NO:1, an A at nucleotide 1043 of SEQ ID NO:1, a T at nucleotide 1094 of SEQ ID NO:1, an A at nucleotide 1125 of SEQ ID NO:1, a T at nucleotide 1469 of SEQ ID NO:1, an insertion of two nucleotides between nucleotides 975 and 976 of SEQ ID NO:1, an insertion of 5 nucleotides after nucleotide 2736 of SEQ ID NO:1, a deletion of 13 nucleotides consisting of nucleotides 1691-1703 of SEQ ID NO:1, an A rather than a G at the 3' end of the intron which interrupts codon 544 of KCNQ2, a mutation causing a stop codon at or before codon 319 of SEQ ID NO:2, a mutation causing a stop codon at or before codon 524 of SEQ ID NO:2, a mutation causing a stop codon at or before codon 323 of SEQ ID NO:2, a mutation causing a stop codon at or before codon 448 of SEQ ID NO:2, a T at nucleotide 947 of SEQ ID NO:6, and the presence of alternative exon of SEQ ID NO:92 in mRNA of KCNQ3. 5. An isolated nucleic acid according to claim 3 wherein said isolated nucleic acid encodes a cysteine at codon 284 of SEQ ID NO:2, a threonine at codon 306 of SEQ ID NO:2, a glutamine at codon 333 of SEQ ID NO:2 or a valine at codon 310 of SEQ ID NO:7. 6. A cell transfected with the isolated nucleic acid of claim 1. 7. A cell transfected with the isolated nucleic acid of claim 2. 8. A cell transfected with the isolated nucleic acid of claim 3. 9. A nucleic acid vector comprising nucleic acid encoding the polypeptide of SEQ ID NO:2 or SEQ ID NO:7. 10. A nucleic acid vector comprising nucleic acid encoding a mutant human KCNQ2 polypeptide or a mutant human KCNQ3 polypeptide. 11. The nucleic acid vector of claim 10 wherein said mutant human KCNQ2 comprises a mutation selected from the group consisting of a G at nucleotide 978 of SEQ ID NO:1, an A at nucleotide 1043 of SEQ ID NO:1, a T at nucleotide 1094 of SEQ ID NO:1, an A at nucleotide 1125 of SEQ ID NO:1, a T at nucleotide 1469 of SEQ ID NO:1, an insertion of two nucleotides between nucleotides 975 and 976 of SEQ ID NO 1, an insertion of 5 nucleotides after nucleotide 2736 of SEQ ID NO:1, a deletion of 13 nucleotid s consisting of nucleotides 1691-1703 of SEQ ID NO:1, an A rather than a G at the 3' end of the intron which interrupts codon 544 of KCNQ2, wherein said mutant human KCNQ3 comprises a T at the nucleotide represented by nucleotide 947 of SEQ ID NO:6, or wherein said mutant huntan KCNQ3 comprises the presence of alternative exon of SEQ ID NO:92 in mRNA of KCNQ3. 12. A method to screen for drugs which modulate K.sup.+ current in cells comprising: a) placing cells comprising wild-type KCNQ2 or wild-type KCNQ3 into a bathing solution to measure current; b) measuring an induced K.sup.+ current in the cells of step (a); c) adding a drug to the bathing solution of step (a); d) measuring an induced K.sup.+ current in the cells of step (c); and e) determining whether the drug resulted in an induced K.sup.+ current in step (d) which differs from the induced K.sup.+ current measured in step (b), wherein a drug which results in the induced currents of steps (b) and (d) differing from each other is a drug which modulates K.sup.+ current in the cells. 13. The method of claim 12 wherein said cells are mammalian. 14. The method of claim 12 wherein said cells are CHO cells. 15. The method according to claim 12 wherein the cells of step (a) have been transfected with human KCNQ2 RNA or human KCNQ3 RNA. 16. A method to screen for drugs which modulate K.sup.+ current in cells comprising: a) placing cells comprising mutant KCNQ2 or mutant KCNQ3 into a bathing solution to measure current; b) measuring an induced K.sup.+ current in the cells of step (a); c) adding a drug to the bathing solution of step (a); d) measuring an induced K.sup.+ current in the cells of step (c); and e) determining whether the drug resulted in an induced K.sup.+ current in step (d) which differs from the induced K.sup.+ current measured in step (b), wherein a drug which results in the induced currents of steps (b) and (d) differing from each other is a drug which modulates K.sup.+ current in the cells. 17. The method of claim 16 wherein said mutant KCNQ2 comprises a mutation selected from the group consisting of a G at nucleotide 978 of SEQ ID NO:1, an A at nucleotide 1043 of SEQ ID NO:1, a T at nucleotide 1094 of SEQ ID NO:1, an A at nucleotide 1125 of SEQ ID NO:1, a T at nucleotide 1469 of SEQ ID NO:1, an insertion df two nucleotides between nucleotides 975 and 976 of SEQ ID NO:1, an insertion of 5 nucleotides after nucleotide 2736 of SEQ ID NO:1, a deletion of 13 nucleotides consisting of nucleotides 1691-1703 of SEQ ID NO:1, an A rather than a G at the 3' end of the intron which interrupts codon 544 of KCNQ2, said mutant KCNQ3 comprises a T at nucleotide 947 of SEQ ID NO:6, or said mutant KCNQ3 comprises the presence of alternative exon of SEQ ID NO:92 in MRNA of KCNQ3. 18. The method of claim 16 wherein said cells are mammalian. 19. The method of claim 16 wherein said cells are CHO cells. 20. The method according to claim 16 wherein the cells of step (a) have been transfected with human KCNQ2 RNA or human KCNQ3 RNA.

Details for Patent 6,413,719

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132	06/04/1986		2017-10-24
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	For Injection	103132			2017-10-24
Merck Sharp & Dohme Corp.	INTRON A	interferon alfa-2b	Injection	103132			2017-10-24