Mutations in and genomic structure of HERG - a long QT syndrome gene
OwnerMark Keating, Igor Splawskiinventors
Life of this patent
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Abstract
The invention relates to the determination of the genomic structure of HERG which is a gene associated with long QT syndrome. The sequences of the 15 intron/exon junctions has been determined and this information is useful in devising primers for amplifying and sequencing across all of the exons of the gene. This is useful for determining the presence or absence of mutations which are known to cause long QT syndrome. Also disclosed are many new mutations in HERG which have been found to be associated with long QT syndrome.
Claims30
An isolated DNA comprising nucleic acid of SEQ ID NO:1 comprising an alteration wherein said alteration is selected from the group consisting of T at position 1714, G at position 1762, T at position 1841, C at position 1955. and all mutations listed in Table 7.
A method for diagnosing a mutation which causes long QT syndrome comprising using a single-stranded conformation polymorphism technique to assay for said mutation wherein said method uses a primer pair selected from the group consisting of:
- 1) SEQ ID NOs:56 and 57;
- 2) SEQ ID NOs:58 and 59;
- 3) SEQ ID NOs:60 and 61;
- 4) SEQ ID NOs:62 and 63;
- 5) SEQ ID NOs:64 and 65;
- 6) SEQ ID NOs:66 and 67;
- 7) SEQ ID NOs:68 and 69;
- 8) SEQ ID NOs:70 and 71;
- 9) SEQ ID NOs:72 and 73;
- 10) SEQ ID NOs:74 and 75;
- 11) SEQ ID NOs:76 and 77;
- 12) SEQ ID NOs:78 and 79;
- 13) SEQ ID NOs:80 and 81;
- 14) SEQ ID NOs:82 and 83;
- 15) SEQ ID NOs:84 and 85;
- 16) SEQ ID NOs:86 and 87;
- 17) SEQ ID NOs:88 and 89;
- 18) SEQ ID NOs:90 and 91;
- 19) SEQ ID NOs:92 and 93;
- and
- 20) SEQ ID NOs:94 and 95.
A method for diagnosing a mutation which causes long QT syndrome comprising amplifying a region of the HERG gene or RNA and sequencing the amplified gene or RNA wherein long QT syndrome is indicated by any one or more mutations of the following group:
- a T at base 1714 of SEQ ID NO:1, a G at base 1762 of SEQ ID NO:1, a T at 1841 of SEQ ID NO:
- 1, a C at base 1889 of SEQ ID NO:1, and a mutation shown in Table 7.
A method for diagnosing a mutation which causes long QT syndrome comprising identifying a mismatch between a patient's DNA or RNA and a wild-type DNA or RNA probe wherein said probe hybridizes to a region of DNA or RNA wherein said region is any one of the following group:
- a region comprising base 1714 of SEQ ID NO:1, base 1762 of SEQ ID NO:1, base 1841 of SEQ ID NO:1. base 1889 of SEQ ID NO:1, and mutations shown in Table 7.
An antibody which binds to a mutant HERG polypeptide but not to wild-type HERG polypeptide, wherein said mutant polypeptide causes long QT syndrome and wherein said mutant polypeptide is a polypeptide of SEQ ID NO:2 wherein said polypeptide has a mutation selected from the group consisting of a cysteine at amino acid residue 572, an aspartic acid at amino acid residue 588, a valine at amino acid residue 614, an alanine at amino acid residue 630, and mutations shown in Table 7.
An isolated HERG polypeptide comprising a mutation which causes long QT syndrome wherein said mutation is a cysteine at amino acid residue 572, an aspartic acid at amino acid residue 588, a valine at amino acid residue 614, an alanine at amino acid residue 630, or a mutation shown in Table 7.
A method for diagnosing long QT syndrome, said method comprising a HERG polypeptide, a mutation in said polypeptide being indicative of long QT syndrome wherein said mutation is selected from the group consisting of a cysteine at amino acid residue 572, an aspartic acid at amino acid residue 588, a valine at amino acid residue 614, an alanine at amino acid residue 630, and mutations shown in Table 7.
A pair of nucleic acids selected from the group consisting of:
- 1) SEQ ID NOs:56 and 57;
- 2) SEQ ID NOs:58 and 59;
- 3) SEQ ID NOs:60 and 61;
- 4) SEQ ID NOs:62 and 63;
- 5) SEQ ID NOs:64 and 65;
- 6) SEQ ID NOs:66 and 67;
- 7) SEQ ID NOs:68 and 69;
- 8) SEQ ID NOs:70 and 71;
- 9) SEQ ID NOs:72 and 73;
- 10) SEQ ID NOs:74 and 75;
- 11) SEQ ID NOs:76 and 77;
- 12) SEQ ID NOs:78 and 79;
- 13) SEQ ID NOs:80 and 81;
- 14) SEQ ID NOs:82 and 83;
- 15) SEQ ID NOs:84 and 85;
- 16) SEQ ID NOs:86 and 87;
- 17) SEQ ID NOs:88 and 89;
- 18) SEQ ID NOs:90 and 91;
- 19) SEQ ID NOs:92 and 93;
- and
- 20) SEQ ID NOs:94 and 95.
An isolated nucleic acid comprising SEQ ID NO:3.
A method to screen for drugs which are useful in treating a person with a mutation in HERG , wherein said mutation is one which results in a cysteine at amino acid residue 572, an aspartic acid at amino acid residue 588, a valine at amino acid residue 614, an alanine at amino acid residue 630, or a mutation shown in Table 7, said method comprising:
- a) placing a first set of cells expressing HERG with a mutation, wherein said mutation is a cysteine at amino acid residue 572, an aspartic acid at amino acid residue 588, a valine at amino acid residue 614, an alanine at amino acid residue 630, or a mutation shown in Table 7, into a bathing solution to measure a first induced K+ current;
- b) measuring said first induced K+ current;
- c) placing a second set of cells expressing wild-type HERG into a bathing solution to measure a second induced K+ current;
- d) measuring said second induced K+ current;
- e) adding a drug to the bathing solution of step (a);
- f) measuring a third induced K− current of cells in step (e);
- and
- g) determining whether the third induced K+ current is more similar to the second induced K+ current than is the first induced K+ current, wherein drugs resulting in a third induced K+ current which is closer to the second induced K+ current than is the first induced K+ current are useful in treating said persons.
Dependencies are inferred from the claim text.