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Molecular biological approaches to neurological disorders including knockout and transgenic mouse models
Author(s) -
Shibata Noriyuki,
Oda Hideaki,
Hirano Asao,
Kato Yoichiro,
Kawaguchi Motoko,
Dal Canto Mauro C,
Uchida Koji,
Sawada Tatsuo,
Kobayashi Makio
Publication year - 2002
Publication title -
neuropathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.701
H-Index - 61
eISSN - 1440-1789
pISSN - 0919-6544
DOI - 10.1046/j.1440-1789.2002.00449.x
Subject(s) - blot , southern blot , agarose gel electrophoresis , microbiology and biotechnology , biology , complementary dna , northern blot , in situ hybridization , genomic dna , gene , messenger rna , polymerase chain reaction , gene expression , genetics
Advances of molecular biology have provided a great variety of new approaches to research on human disorders. This article gives an outline of molecular biological approaches to analysis of neurological disorders such as giant cell glioblastoma (GGBM) and amyotrophic lat‐eral sclerosis (ALS), and their respective animal models: p53 knockout mice for GGBM and mutant superoxide dismutase‐1 transgenic mice for ALS. Genomic DNA extracted from fresh‐frozen tissue is examined by Southern blotting for screening mutations in a certain gene. Polymerase chain reaction (PCR) products of a gene in genomic DNA are examined by single‐stranded conformation polymorphism, sequencing and agarose gel electrophoresis for identifying mutations, and for preparing and evaluating DNA probes used in Southern blotting and DNA in situ hybridization (ISH). Total RNA from tissue is examined by northern blotting for quantifying and verifying a certain mRNA. Reverse transcription‐PCR products of a certain mRNA in total RNA are examined by sequencing and agarose gel electrophoresis for preparing and evaluating cDNA probes used in northern blotting and mRNA ISH. Tissue total protein is immunoblotted for quantifying and verifying a certain protein, and for evaluating the specificity of antibodies used in western blotting and immunohistochemistry. Immunoprecipitates are im‐munoblotted for evaluating a profile of protein or other substances. Enzyme‐linked immunosorbent assay is used for measuring tissue concentration of protein or other substances, and for determining titers of specific antibodies. By these procedures, chronological analysis of animal models for human diseases contribute to elucidating pathogenic mechanisms and exploiting new therapies. Noticing both the similarity and difference between human and animal disorders will help understand the nature of disease.