Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1
Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from a...
Gespeichert in:
Veröffentlicht in: | Muscle & nerve 2013-07, Vol.48 (1), p.105-108 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 108 |
---|---|
container_issue | 1 |
container_start_page | 105 |
container_title | Muscle & nerve |
container_volume | 48 |
creator | Jinnai, Kenji Mitani, Maki Futamura, Naonobu Kawamoto, Kunihiko Funakawa, Itaru Itoh, Kyoko |
description | Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. Muscle Nerve, 2013 |
doi_str_mv | 10.1002/mus.23717 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1439228679</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1439228679</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4907-bc5665bdf6a988e2a09a05524bc989592dad98b7a99fa6706ba6448d39eb4e513</originalsourceid><addsrcrecordid>eNqFkUtP3DAUhS1UVAbaRf9AFYkNLAJ-P5YogmlVKFSAYGfZiSNCk3GwHdH8-3o6wKJS1dVd3O-c-zgAfELwCEGIj4cpHmEikNgCCwSVKClT8h1YQERlyYm63wG7MT5CCJHk4j3YwYRjJaFYgB_XfjCpq4tuFZOxXd-lufBtUd0si-BGZ1LMrSI9uKJ2wVnX99OwBobZJ7_KwmaOKfjxYS7SPLoCfQDbremj-_hS98Dt2elN9aU8v1x-rU7Oy5oqKEpbM86ZbVpulJQOG6gMZAxTWyupmMKNaZS0wijVGi4gt4ZTKhuinKWOIbIHDja-Y_BPk4tJD12s835m5fwUNaJEYZzvVf9H8--wQAyTjO7_hT76KazyIWsKYkq5WM8-3FB18DEG1-oxdIMJs0ZQryPRORL9J5LMfn5xnOzgmjfyNYMMHG-A565387-d9MXt9atluVF0MblfbwoTfmouiGD67vtSk4ot777JK12R384xoxI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1370244671</pqid></control><display><type>article</type><title>Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Jinnai, Kenji ; Mitani, Maki ; Futamura, Naonobu ; Kawamoto, Kunihiko ; Funakawa, Itaru ; Itoh, Kyoko</creator><creatorcontrib>Jinnai, Kenji ; Mitani, Maki ; Futamura, Naonobu ; Kawamoto, Kunihiko ; Funakawa, Itaru ; Itoh, Kyoko</creatorcontrib><description>Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. Muscle Nerve, 2013</description><identifier>ISSN: 0148-639X</identifier><identifier>EISSN: 1097-4598</identifier><identifier>DOI: 10.1002/mus.23717</identifier><identifier>PMID: 23629807</identifier><identifier>CODEN: MUNEDE</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Aged ; Brain ; cerebellum ; Cerebellum - pathology ; Cerebellum - physiology ; CTG repeat ; Female ; Humans ; Male ; Middle Aged ; Muscular dystrophy ; Myotonic Dystrophy - genetics ; Myotonic Dystrophy - pathology ; myotonic dystrophy type 1 ; somatic instability ; Trinucleotide Repeat Expansion - genetics</subject><ispartof>Muscle & nerve, 2013-07, Vol.48 (1), p.105-108</ispartof><rights>Copyright © 2012 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4907-bc5665bdf6a988e2a09a05524bc989592dad98b7a99fa6706ba6448d39eb4e513</citedby><cites>FETCH-LOGICAL-c4907-bc5665bdf6a988e2a09a05524bc989592dad98b7a99fa6706ba6448d39eb4e513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmus.23717$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmus.23717$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23629807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jinnai, Kenji</creatorcontrib><creatorcontrib>Mitani, Maki</creatorcontrib><creatorcontrib>Futamura, Naonobu</creatorcontrib><creatorcontrib>Kawamoto, Kunihiko</creatorcontrib><creatorcontrib>Funakawa, Itaru</creatorcontrib><creatorcontrib>Itoh, Kyoko</creatorcontrib><title>Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1</title><title>Muscle & nerve</title><addtitle>Muscle Nerve</addtitle><description>Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. Muscle Nerve, 2013</description><subject>Aged</subject><subject>Brain</subject><subject>cerebellum</subject><subject>Cerebellum - pathology</subject><subject>Cerebellum - physiology</subject><subject>CTG repeat</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Muscular dystrophy</subject><subject>Myotonic Dystrophy - genetics</subject><subject>Myotonic Dystrophy - pathology</subject><subject>myotonic dystrophy type 1</subject><subject>somatic instability</subject><subject>Trinucleotide Repeat Expansion - genetics</subject><issn>0148-639X</issn><issn>1097-4598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtP3DAUhS1UVAbaRf9AFYkNLAJ-P5YogmlVKFSAYGfZiSNCk3GwHdH8-3o6wKJS1dVd3O-c-zgAfELwCEGIj4cpHmEikNgCCwSVKClT8h1YQERlyYm63wG7MT5CCJHk4j3YwYRjJaFYgB_XfjCpq4tuFZOxXd-lufBtUd0si-BGZ1LMrSI9uKJ2wVnX99OwBobZJ7_KwmaOKfjxYS7SPLoCfQDbremj-_hS98Dt2elN9aU8v1x-rU7Oy5oqKEpbM86ZbVpulJQOG6gMZAxTWyupmMKNaZS0wijVGi4gt4ZTKhuinKWOIbIHDja-Y_BPk4tJD12s835m5fwUNaJEYZzvVf9H8--wQAyTjO7_hT76KazyIWsKYkq5WM8-3FB18DEG1-oxdIMJs0ZQryPRORL9J5LMfn5xnOzgmjfyNYMMHG-A565387-d9MXt9atluVF0MblfbwoTfmouiGD67vtSk4ot777JK12R384xoxI</recordid><startdate>201307</startdate><enddate>201307</enddate><creator>Jinnai, Kenji</creator><creator>Mitani, Maki</creator><creator>Futamura, Naonobu</creator><creator>Kawamoto, Kunihiko</creator><creator>Funakawa, Itaru</creator><creator>Itoh, Kyoko</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TS</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201307</creationdate><title>Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1</title><author>Jinnai, Kenji ; Mitani, Maki ; Futamura, Naonobu ; Kawamoto, Kunihiko ; Funakawa, Itaru ; Itoh, Kyoko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4907-bc5665bdf6a988e2a09a05524bc989592dad98b7a99fa6706ba6448d39eb4e513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aged</topic><topic>Brain</topic><topic>cerebellum</topic><topic>Cerebellum - pathology</topic><topic>Cerebellum - physiology</topic><topic>CTG repeat</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Muscular dystrophy</topic><topic>Myotonic Dystrophy - genetics</topic><topic>Myotonic Dystrophy - pathology</topic><topic>myotonic dystrophy type 1</topic><topic>somatic instability</topic><topic>Trinucleotide Repeat Expansion - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jinnai, Kenji</creatorcontrib><creatorcontrib>Mitani, Maki</creatorcontrib><creatorcontrib>Futamura, Naonobu</creatorcontrib><creatorcontrib>Kawamoto, Kunihiko</creatorcontrib><creatorcontrib>Funakawa, Itaru</creatorcontrib><creatorcontrib>Itoh, Kyoko</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Muscle & nerve</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jinnai, Kenji</au><au>Mitani, Maki</au><au>Futamura, Naonobu</au><au>Kawamoto, Kunihiko</au><au>Funakawa, Itaru</au><au>Itoh, Kyoko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1</atitle><jtitle>Muscle & nerve</jtitle><addtitle>Muscle Nerve</addtitle><date>2013-07</date><risdate>2013</risdate><volume>48</volume><issue>1</issue><spage>105</spage><epage>108</epage><pages>105-108</pages><issn>0148-639X</issn><eissn>1097-4598</eissn><coden>MUNEDE</coden><abstract>Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. Muscle Nerve, 2013</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23629807</pmid><doi>10.1002/mus.23717</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0148-639X |
ispartof | Muscle & nerve, 2013-07, Vol.48 (1), p.105-108 |
issn | 0148-639X 1097-4598 |
language | eng |
recordid | cdi_proquest_miscellaneous_1439228679 |
source | MEDLINE; Wiley Online Library All Journals |
subjects | Aged Brain cerebellum Cerebellum - pathology Cerebellum - physiology CTG repeat Female Humans Male Middle Aged Muscular dystrophy Myotonic Dystrophy - genetics Myotonic Dystrophy - pathology myotonic dystrophy type 1 somatic instability Trinucleotide Repeat Expansion - genetics |
title | Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T16%3A08%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Somatic%20instability%20of%20CTG%20repeats%20in%20the%20cerebellum%20of%20myotonic%20dystrophy%20type%201&rft.jtitle=Muscle%20&%20nerve&rft.au=Jinnai,%20Kenji&rft.date=2013-07&rft.volume=48&rft.issue=1&rft.spage=105&rft.epage=108&rft.pages=105-108&rft.issn=0148-639X&rft.eissn=1097-4598&rft.coden=MUNEDE&rft_id=info:doi/10.1002/mus.23717&rft_dat=%3Cproquest_cross%3E1439228679%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1370244671&rft_id=info:pmid/23629807&rfr_iscdi=true |