Analysis of the CAG Repeat Number in a Patient with Huntington's Disease
This study was performed to confirm 1) the difference in the trinucleotide CAG repeat number among tissues, 2) somatic mosaicism in each tissue, 3) the correlation of the repeat number with pathological severity in Huntington's disease. The CAG repeat number was determined by analysis of the po...
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Veröffentlicht in: | Internal Medicine 1999, Vol.38(5), pp.407-411 |
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creator | KONO, Yasuhisa AGAWA, Yasuo WATANABE, Yasuhiro OHAMA, Eisaku NANBA, Eiji NAKASHIMA, Kenji |
description | This study was performed to confirm 1) the difference in the trinucleotide CAG repeat number among tissues, 2) somatic mosaicism in each tissue, 3) the correlation of the repeat number with pathological severity in Huntington's disease. The CAG repeat number was determined by analysis of the polymerase chain reaction (PCR) product in various tissues, including central nervous system (CNS) tissues and non-CNS tissues. We also determined the pathological severity grade in each brain section and compared this with the results of CAG repeat analyses. The patient was a Japanese male with Huntington's disease who died at 62 years of age. Genomic DNA was extracted from 10 parts of the central nervous system and 6 parts of other tissues from the patient. Each part of the formalin-fixed brain was subjected to gross and microscopic pathological assessment. The main peaks of CAG repeat in all tissues were 22 and 44. In analysis of somatic mosaicism, high degrees of mosaicism were obtained in the caudate nucleus, putamen and cerebral cortex, in which more severe degeneration was observed by pathological examination. These results, although this is a single case study, indicated that pathological severity did not correlate with the CAG repeat number, but it did relate to the degree of somatic mosaicism. Somatic mosaicism might reflect region-specific neuronal degeneration in Huntington's disease. (Internal Medicine 38: 407-411, 1999) |
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The CAG repeat number was determined by analysis of the polymerase chain reaction (PCR) product in various tissues, including central nervous system (CNS) tissues and non-CNS tissues. We also determined the pathological severity grade in each brain section and compared this with the results of CAG repeat analyses. The patient was a Japanese male with Huntington's disease who died at 62 years of age. Genomic DNA was extracted from 10 parts of the central nervous system and 6 parts of other tissues from the patient. Each part of the formalin-fixed brain was subjected to gross and microscopic pathological assessment. The main peaks of CAG repeat in all tissues were 22 and 44. In analysis of somatic mosaicism, high degrees of mosaicism were obtained in the caudate nucleus, putamen and cerebral cortex, in which more severe degeneration was observed by pathological examination. These results, although this is a single case study, indicated that pathological severity did not correlate with the CAG repeat number, but it did relate to the degree of somatic mosaicism. Somatic mosaicism might reflect region-specific neuronal degeneration in Huntington's disease. (Internal Medicine 38: 407-411, 1999)</description><identifier>ISSN: 0918-2918</identifier><identifier>EISSN: 1349-7235</identifier><identifier>DOI: 10.2169/internalmedicine.38.407</identifier><identifier>PMID: 10397077</identifier><language>eng</language><publisher>Tokyo: The Japanese Society of Internal Medicine</publisher><subject>Biological and medical sciences ; Brain - pathology ; Brain Chemistry ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; DNA - analysis ; DNA Primers - chemistry ; Humans ; Huntington Disease - genetics ; Huntington Disease - pathology ; Male ; Medical sciences ; Middle Aged ; Mosaicism - genetics ; neurodegeneration ; Neurology ; Polymerase Chain Reaction ; somatic mosaicism ; Trinucleotide Repeats - genetics ; triplet repeat disease</subject><ispartof>Internal Medicine, 1999, Vol.38(5), pp.407-411</ispartof><rights>The Japanese Society of Internal Medicine</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-d440092c8a78159302b845364923b12f3a51845f7993ea9db7b5d55ac788817d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,1879,4012,27906,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1914988$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10397077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KONO, Yasuhisa</creatorcontrib><creatorcontrib>AGAWA, Yasuo</creatorcontrib><creatorcontrib>WATANABE, Yasuhiro</creatorcontrib><creatorcontrib>OHAMA, Eisaku</creatorcontrib><creatorcontrib>NANBA, Eiji</creatorcontrib><creatorcontrib>NAKASHIMA, Kenji</creatorcontrib><title>Analysis of the CAG Repeat Number in a Patient with Huntington's Disease</title><title>Internal Medicine</title><addtitle>Intern. Med.</addtitle><description>This study was performed to confirm 1) the difference in the trinucleotide CAG repeat number among tissues, 2) somatic mosaicism in each tissue, 3) the correlation of the repeat number with pathological severity in Huntington's disease. The CAG repeat number was determined by analysis of the polymerase chain reaction (PCR) product in various tissues, including central nervous system (CNS) tissues and non-CNS tissues. We also determined the pathological severity grade in each brain section and compared this with the results of CAG repeat analyses. The patient was a Japanese male with Huntington's disease who died at 62 years of age. Genomic DNA was extracted from 10 parts of the central nervous system and 6 parts of other tissues from the patient. Each part of the formalin-fixed brain was subjected to gross and microscopic pathological assessment. The main peaks of CAG repeat in all tissues were 22 and 44. In analysis of somatic mosaicism, high degrees of mosaicism were obtained in the caudate nucleus, putamen and cerebral cortex, in which more severe degeneration was observed by pathological examination. These results, although this is a single case study, indicated that pathological severity did not correlate with the CAG repeat number, but it did relate to the degree of somatic mosaicism. Somatic mosaicism might reflect region-specific neuronal degeneration in Huntington's disease. (Internal Medicine 38: 407-411, 1999)</description><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Brain Chemistry</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>DNA - analysis</subject><subject>DNA Primers - chemistry</subject><subject>Humans</subject><subject>Huntington Disease - genetics</subject><subject>Huntington Disease - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mosaicism - genetics</subject><subject>neurodegeneration</subject><subject>Neurology</subject><subject>Polymerase Chain Reaction</subject><subject>somatic mosaicism</subject><subject>Trinucleotide Repeats - genetics</subject><subject>triplet repeat disease</subject><issn>0918-2918</issn><issn>1349-7235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNplkE9v1DAQxS0EotvCVwAfEJyy-E8c28fVFrpIFVQIztHEmXRdZZ3FdlT12-Mqq4LgMiPN_Gbe0yPkLWdrwRv70YeMMcB4wN47H3Atzbpm-hlZcVnbSgupnpMVs9xUopQzcp7SHWPSaCtekjPOpNVM6xXZbcqXh-QTnQaa90i3myv6HY8ImX6dDx1G6gMFegPZY8j03uc93c0h-3Cbp_Ah0UufEBK-Ii8GGBO-PvUL8vPzpx_bXXX97erLdnNdOSWaXPV1zZgVzoA2XFnJRGdqJZvaCtlxMUhQvAwGba1EsH2nO9UrBU4bY7ju5QV5v_w9xunXjCm3B58cjiMEnObUNtYYZhpRQL2ALk4pRRzaY_QHiA8tZ-1jiO2_IbbStCXEcvnmJDF3ZffX3ZJaAd6dAEgOxiFCcD794Syvi4uC3SzYXcpwi097iNm7Ef_T59aKRw9qKcXKE-r2EFsM8jdiHZrT</recordid><startdate>1999</startdate><enddate>1999</enddate><creator>KONO, Yasuhisa</creator><creator>AGAWA, Yasuo</creator><creator>WATANABE, Yasuhiro</creator><creator>OHAMA, Eisaku</creator><creator>NANBA, Eiji</creator><creator>NAKASHIMA, Kenji</creator><general>The Japanese Society of Internal Medicine</general><general>Japanese Society of Internal Medicine</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1999</creationdate><title>Analysis of the CAG Repeat Number in a Patient with Huntington's Disease</title><author>KONO, Yasuhisa ; AGAWA, Yasuo ; WATANABE, Yasuhiro ; OHAMA, Eisaku ; NANBA, Eiji ; NAKASHIMA, Kenji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-d440092c8a78159302b845364923b12f3a51845f7993ea9db7b5d55ac788817d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Biological and medical sciences</topic><topic>Brain - pathology</topic><topic>Brain Chemistry</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>DNA - analysis</topic><topic>DNA Primers - chemistry</topic><topic>Humans</topic><topic>Huntington Disease - genetics</topic><topic>Huntington Disease - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mosaicism - genetics</topic><topic>neurodegeneration</topic><topic>Neurology</topic><topic>Polymerase Chain Reaction</topic><topic>somatic mosaicism</topic><topic>Trinucleotide Repeats - genetics</topic><topic>triplet repeat disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KONO, Yasuhisa</creatorcontrib><creatorcontrib>AGAWA, Yasuo</creatorcontrib><creatorcontrib>WATANABE, Yasuhiro</creatorcontrib><creatorcontrib>OHAMA, Eisaku</creatorcontrib><creatorcontrib>NANBA, Eiji</creatorcontrib><creatorcontrib>NAKASHIMA, Kenji</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Internal Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KONO, Yasuhisa</au><au>AGAWA, Yasuo</au><au>WATANABE, Yasuhiro</au><au>OHAMA, Eisaku</au><au>NANBA, Eiji</au><au>NAKASHIMA, Kenji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of the CAG Repeat Number in a Patient with Huntington's Disease</atitle><jtitle>Internal Medicine</jtitle><addtitle>Intern. 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Each part of the formalin-fixed brain was subjected to gross and microscopic pathological assessment. The main peaks of CAG repeat in all tissues were 22 and 44. In analysis of somatic mosaicism, high degrees of mosaicism were obtained in the caudate nucleus, putamen and cerebral cortex, in which more severe degeneration was observed by pathological examination. These results, although this is a single case study, indicated that pathological severity did not correlate with the CAG repeat number, but it did relate to the degree of somatic mosaicism. Somatic mosaicism might reflect region-specific neuronal degeneration in Huntington's disease. (Internal Medicine 38: 407-411, 1999)</abstract><cop>Tokyo</cop><pub>The Japanese Society of Internal Medicine</pub><pmid>10397077</pmid><doi>10.2169/internalmedicine.38.407</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Brain - pathology Brain Chemistry Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases DNA - analysis DNA Primers - chemistry Humans Huntington Disease - genetics Huntington Disease - pathology Male Medical sciences Middle Aged Mosaicism - genetics neurodegeneration Neurology Polymerase Chain Reaction somatic mosaicism Trinucleotide Repeats - genetics triplet repeat disease |
title | Analysis of the CAG Repeat Number in a Patient with Huntington's Disease |
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