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Methods for identification of alport syndrome

a technology of alport syndrome and methods, applied in the field of gene testing in dogs, can solve the problems of improper assembly and non-identification of causal mutations in these genes

Inactive Publication Date: 2007-10-18
LEES GEORGE E +2
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Problems solved by technology

However, the causative mutations in these genes have not been identified.
Defects in any one of the three α chains in a heterotrimer impedes proper assembly and prevents deposition, of any of the proteins involved, into the GBM.

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  • Methods for identification of alport syndrome
  • Methods for identification of alport syndrome
  • Methods for identification of alport syndrome

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[0012]“Genetic marker” or “marker” as used herein refers to a variable or polymorphic nucleotide sequence that is present in genomic DNA, and which is identifiable with specific oligonucleotides (e.g., distinguishable by nucleic acid amplification and observance of a difference in size or sequence of nucleotides due to the polymorphism). The “locus” of a genetic marker or marker refers to its place on the chromosome in relation to another locus. Markers, as illustrated herein, can be identified by any one of several techniques know to those skilled in the art, including microsatellite or short tandem repeat (STR) amplification, analyses of restriction fragment length polymorphisms (RFLP), single nucleotide polymorphism (SNP), detection of deletion or insertion sites, and random amplified polymorphic DNA (RAPD) analysis.

[0013]“Co-segregate” as used herein refers to inheritance together of two specific loci; e.g., the loci are located so physically close on the same chro...

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Abstract

Animals with mutations in COL4α4 present with autosomal recessive Alport Syndrome (ARAS). Through sequencing of COL4α4, the mutation causative for ARAS in the English Cocker Spaniel (ECS) has been identified. The resulting protein is severely truncated due to a premature stop codon in exon 3. This nonsense mutation occurs in the 7S domain and also causes the loss of the entire collagenous and NC1 domains of the protein. Methods for the identification of animals that harbor a mutation in the COL4α4 gene are described. Mutations in the COL4α4 gene can be identified from any biological sample such as a cell or tissue that contains genomic DNA. Methods for identifying single nucleotide polymorphisms (SNPs) that are inherited with the disease are also described. A microsatellite marker that segregates with ARAS is also described that was identified using linkage disequilibrium mapping.

Description

[0001] This application claims priority to U.S. Ser. No. 60 / 790,115 filed Apr. 7, 2006.BACKGROUND OF THE INVENTION [0002] The present invention is generally in the field of genetic testing in dogs, and is specifically a genetic test for the mutation that causes Alport Syndrome (AS) or for a marker associated with the mutation. [0003] Alport Syndrome (AS) is hereditary progressive glomerular nephritis which affects both humans and several breeds of domestic dogs. This disease is caused by mutations in the genes that encode certain proteins in the type IV collagen family. The type IV collagen family includes six distinct chains (α1-α6) which are major constituents of mammalian basement membranes throughout the body. AS specifically affects the glomerular basement membrane (GBM) of the kidney, causing a distinctive multilaminar splitting of the GBM ultrastructure, characteristic to the disease. These defects in the GBM contribute to the development of hematuria, proteinuria, and progre...

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12Q1/68C12P19/34
CPCC12Q1/6883C12Q2600/172C12Q2600/156
Inventor MURPHY, KEITH E.DAVIDSON, ASHLEY G.LEES, GEORGE E.
Owner LEES GEORGE E
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