Loading…

The Huntington's Disease Gene Discovery

The gene for Huntington's disease (HD) was discovered in 1993, after an international collaborative initiative that led researchers to remote regions of South America. It was the most remarkable milestone, since George Huntington's initial description. Through the phenomenological discussi...

Full description

Saved in:
Bibliographic Details
Published in:Movement disorders 2024-02, Vol.39 (2), p.227-234
Main Authors: Franklin, Gustavo L., Teive, Hélio A.G., Tensini, Fernando Spina, Camargo, Carlos Henrique Ferreira, Lima, Nayra de Souza Carvalho, dos Santos, Diego de Castro, Meira, Alex T., Tabrizi, Sarah J.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c3133-eb7622a957174ea82b689e1a4c8f8540f813da7af98280ea9518890658ffdfea3
container_end_page 234
container_issue 2
container_start_page 227
container_title Movement disorders
container_volume 39
creator Franklin, Gustavo L.
Teive, Hélio A.G.
Tensini, Fernando Spina
Camargo, Carlos Henrique Ferreira
Lima, Nayra de Souza Carvalho
dos Santos, Diego de Castro
Meira, Alex T.
Tabrizi, Sarah J.
description The gene for Huntington's disease (HD) was discovered in 1993, after an international collaborative initiative that led researchers to remote regions of South America. It was the most remarkable milestone, since George Huntington's initial description. Through the phenomenological discussions led by Jean‐Martin Charcot and Willian Osler, and finally Americo Negrette's reports, which served as the inspiration for the Venezuela Project led by Nancy Wexler, the journey toward discovering the Huntington's disease (HD) gene was marked by substantial efforts. This monumental achievement involved the analysis of more than 18,000 blood samples and gathered dozens of researchers in an integrated effort, enabling the mapping of the gene on chromosome 4 in 1983 and leading, a decade later, to the precise localization and identification of the HTT gene. The discovery of the HD mutation represented a pivotal moment in the field of genetics and neurology, significantly enhancing our understanding of the disease and creating opportunities for future treatments. The progress made and the knowledge gained during this journey catalyzed the development of many innovative molecular techniques that have advanced research in other medical conditions. In this article, the authors celebrate three decades of this memorable event, revisiting the historical aspects, providing insights into the techniques developed, and delving into the paths that ultimately led to the discovery of the HD gene. © 2024 International Parkinson and Movement Disorder Society.
doi_str_mv 10.1002/mds.29703
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2928946517</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2928946517</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3133-eb7622a957174ea82b689e1a4c8f8540f813da7af98280ea9518890658ffdfea3</originalsourceid><addsrcrecordid>eNp10M1Kw0AUBeBBFFurC19ACi6qi7Tzk8ncWUqrrVBxYV0P0-SOpqSJZhqlb-_UVBeCq8uFj8PhEHLO6JBRykfrzA-5VlQckC6TgkXApTokXQogI8FAdsiJ9ytKGZMsOSYdAUzphMouGSxesT9ryk1evmyqcuD7k9yj9difYom7J60-sN6ekiNnC49n-9sjz3e3i_Esmj9O78c38ygVTIgIlyrh3GqpmIrRAl8moJHZOAUHMqYOmMissk4DB4oBMgBNEwnOZQ6t6JGrNvetrt4b9BuzDhWwKGyJVeMN1xx0nEimAr38Q1dVU5ehXVCCC04p7NR1q9K68r5GZ97qfG3rrWHU7NYzYT3zvV6wF_vEZrnG7Ff-zBXAqAWfeYHb_5PMw-SpjfwCmn915g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2932320087</pqid></control><display><type>article</type><title>The Huntington's Disease Gene Discovery</title><source>Wiley</source><creator>Franklin, Gustavo L. ; Teive, Hélio A.G. ; Tensini, Fernando Spina ; Camargo, Carlos Henrique Ferreira ; Lima, Nayra de Souza Carvalho ; dos Santos, Diego de Castro ; Meira, Alex T. ; Tabrizi, Sarah J.</creator><creatorcontrib>Franklin, Gustavo L. ; Teive, Hélio A.G. ; Tensini, Fernando Spina ; Camargo, Carlos Henrique Ferreira ; Lima, Nayra de Souza Carvalho ; dos Santos, Diego de Castro ; Meira, Alex T. ; Tabrizi, Sarah J.</creatorcontrib><description>The gene for Huntington's disease (HD) was discovered in 1993, after an international collaborative initiative that led researchers to remote regions of South America. It was the most remarkable milestone, since George Huntington's initial description. Through the phenomenological discussions led by Jean‐Martin Charcot and Willian Osler, and finally Americo Negrette's reports, which served as the inspiration for the Venezuela Project led by Nancy Wexler, the journey toward discovering the Huntington's disease (HD) gene was marked by substantial efforts. This monumental achievement involved the analysis of more than 18,000 blood samples and gathered dozens of researchers in an integrated effort, enabling the mapping of the gene on chromosome 4 in 1983 and leading, a decade later, to the precise localization and identification of the HTT gene. The discovery of the HD mutation represented a pivotal moment in the field of genetics and neurology, significantly enhancing our understanding of the disease and creating opportunities for future treatments. The progress made and the knowledge gained during this journey catalyzed the development of many innovative molecular techniques that have advanced research in other medical conditions. In this article, the authors celebrate three decades of this memorable event, revisiting the historical aspects, providing insights into the techniques developed, and delving into the paths that ultimately led to the discovery of the HD gene. © 2024 International Parkinson and Movement Disorder Society.</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.29703</identifier><identifier>PMID: 38179605</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>chorea ; Chromosome 4 ; gene ; Gene mapping ; genetics ; history of medicine ; Huntingtin ; Huntington's disease ; Huntingtons disease ; Localization</subject><ispartof>Movement disorders, 2024-02, Vol.39 (2), p.227-234</ispartof><rights>2024 International Parkinson and Movement Disorder Society.</rights><rights>2024 International Parkinson and Movement Disorder Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3133-eb7622a957174ea82b689e1a4c8f8540f813da7af98280ea9518890658ffdfea3</cites><orcidid>0000-0003-2716-2045 ; 0000-0002-6685-7491 ; 0000-0002-3533-0347 ; 0000-0002-0207-3671 ; 0000-0002-2592-2779 ; 0000-0002-7595-5878</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38179605$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Franklin, Gustavo L.</creatorcontrib><creatorcontrib>Teive, Hélio A.G.</creatorcontrib><creatorcontrib>Tensini, Fernando Spina</creatorcontrib><creatorcontrib>Camargo, Carlos Henrique Ferreira</creatorcontrib><creatorcontrib>Lima, Nayra de Souza Carvalho</creatorcontrib><creatorcontrib>dos Santos, Diego de Castro</creatorcontrib><creatorcontrib>Meira, Alex T.</creatorcontrib><creatorcontrib>Tabrizi, Sarah J.</creatorcontrib><title>The Huntington's Disease Gene Discovery</title><title>Movement disorders</title><addtitle>Mov Disord</addtitle><description>The gene for Huntington's disease (HD) was discovered in 1993, after an international collaborative initiative that led researchers to remote regions of South America. It was the most remarkable milestone, since George Huntington's initial description. Through the phenomenological discussions led by Jean‐Martin Charcot and Willian Osler, and finally Americo Negrette's reports, which served as the inspiration for the Venezuela Project led by Nancy Wexler, the journey toward discovering the Huntington's disease (HD) gene was marked by substantial efforts. This monumental achievement involved the analysis of more than 18,000 blood samples and gathered dozens of researchers in an integrated effort, enabling the mapping of the gene on chromosome 4 in 1983 and leading, a decade later, to the precise localization and identification of the HTT gene. The discovery of the HD mutation represented a pivotal moment in the field of genetics and neurology, significantly enhancing our understanding of the disease and creating opportunities for future treatments. The progress made and the knowledge gained during this journey catalyzed the development of many innovative molecular techniques that have advanced research in other medical conditions. In this article, the authors celebrate three decades of this memorable event, revisiting the historical aspects, providing insights into the techniques developed, and delving into the paths that ultimately led to the discovery of the HD gene. © 2024 International Parkinson and Movement Disorder Society.</description><subject>chorea</subject><subject>Chromosome 4</subject><subject>gene</subject><subject>Gene mapping</subject><subject>genetics</subject><subject>history of medicine</subject><subject>Huntingtin</subject><subject>Huntington's disease</subject><subject>Huntingtons disease</subject><subject>Localization</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp10M1Kw0AUBeBBFFurC19ACi6qi7Tzk8ncWUqrrVBxYV0P0-SOpqSJZhqlb-_UVBeCq8uFj8PhEHLO6JBRykfrzA-5VlQckC6TgkXApTokXQogI8FAdsiJ9ytKGZMsOSYdAUzphMouGSxesT9ryk1evmyqcuD7k9yj9difYom7J60-sN6ekiNnC49n-9sjz3e3i_Esmj9O78c38ygVTIgIlyrh3GqpmIrRAl8moJHZOAUHMqYOmMissk4DB4oBMgBNEwnOZQ6t6JGrNvetrt4b9BuzDhWwKGyJVeMN1xx0nEimAr38Q1dVU5ehXVCCC04p7NR1q9K68r5GZ97qfG3rrWHU7NYzYT3zvV6wF_vEZrnG7Ff-zBXAqAWfeYHb_5PMw-SpjfwCmn915g</recordid><startdate>202402</startdate><enddate>202402</enddate><creator>Franklin, Gustavo L.</creator><creator>Teive, Hélio A.G.</creator><creator>Tensini, Fernando Spina</creator><creator>Camargo, Carlos Henrique Ferreira</creator><creator>Lima, Nayra de Souza Carvalho</creator><creator>dos Santos, Diego de Castro</creator><creator>Meira, Alex T.</creator><creator>Tabrizi, Sarah J.</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2716-2045</orcidid><orcidid>https://orcid.org/0000-0002-6685-7491</orcidid><orcidid>https://orcid.org/0000-0002-3533-0347</orcidid><orcidid>https://orcid.org/0000-0002-0207-3671</orcidid><orcidid>https://orcid.org/0000-0002-2592-2779</orcidid><orcidid>https://orcid.org/0000-0002-7595-5878</orcidid></search><sort><creationdate>202402</creationdate><title>The Huntington's Disease Gene Discovery</title><author>Franklin, Gustavo L. ; Teive, Hélio A.G. ; Tensini, Fernando Spina ; Camargo, Carlos Henrique Ferreira ; Lima, Nayra de Souza Carvalho ; dos Santos, Diego de Castro ; Meira, Alex T. ; Tabrizi, Sarah J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3133-eb7622a957174ea82b689e1a4c8f8540f813da7af98280ea9518890658ffdfea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>chorea</topic><topic>Chromosome 4</topic><topic>gene</topic><topic>Gene mapping</topic><topic>genetics</topic><topic>history of medicine</topic><topic>Huntingtin</topic><topic>Huntington's disease</topic><topic>Huntingtons disease</topic><topic>Localization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Franklin, Gustavo L.</creatorcontrib><creatorcontrib>Teive, Hélio A.G.</creatorcontrib><creatorcontrib>Tensini, Fernando Spina</creatorcontrib><creatorcontrib>Camargo, Carlos Henrique Ferreira</creatorcontrib><creatorcontrib>Lima, Nayra de Souza Carvalho</creatorcontrib><creatorcontrib>dos Santos, Diego de Castro</creatorcontrib><creatorcontrib>Meira, Alex T.</creatorcontrib><creatorcontrib>Tabrizi, Sarah J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Franklin, Gustavo L.</au><au>Teive, Hélio A.G.</au><au>Tensini, Fernando Spina</au><au>Camargo, Carlos Henrique Ferreira</au><au>Lima, Nayra de Souza Carvalho</au><au>dos Santos, Diego de Castro</au><au>Meira, Alex T.</au><au>Tabrizi, Sarah J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Huntington's Disease Gene Discovery</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov Disord</addtitle><date>2024-02</date><risdate>2024</risdate><volume>39</volume><issue>2</issue><spage>227</spage><epage>234</epage><pages>227-234</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>The gene for Huntington's disease (HD) was discovered in 1993, after an international collaborative initiative that led researchers to remote regions of South America. It was the most remarkable milestone, since George Huntington's initial description. Through the phenomenological discussions led by Jean‐Martin Charcot and Willian Osler, and finally Americo Negrette's reports, which served as the inspiration for the Venezuela Project led by Nancy Wexler, the journey toward discovering the Huntington's disease (HD) gene was marked by substantial efforts. This monumental achievement involved the analysis of more than 18,000 blood samples and gathered dozens of researchers in an integrated effort, enabling the mapping of the gene on chromosome 4 in 1983 and leading, a decade later, to the precise localization and identification of the HTT gene. The discovery of the HD mutation represented a pivotal moment in the field of genetics and neurology, significantly enhancing our understanding of the disease and creating opportunities for future treatments. The progress made and the knowledge gained during this journey catalyzed the development of many innovative molecular techniques that have advanced research in other medical conditions. In this article, the authors celebrate three decades of this memorable event, revisiting the historical aspects, providing insights into the techniques developed, and delving into the paths that ultimately led to the discovery of the HD gene. © 2024 International Parkinson and Movement Disorder Society.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>38179605</pmid><doi>10.1002/mds.29703</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2716-2045</orcidid><orcidid>https://orcid.org/0000-0002-6685-7491</orcidid><orcidid>https://orcid.org/0000-0002-3533-0347</orcidid><orcidid>https://orcid.org/0000-0002-0207-3671</orcidid><orcidid>https://orcid.org/0000-0002-2592-2779</orcidid><orcidid>https://orcid.org/0000-0002-7595-5878</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0885-3185
ispartof Movement disorders, 2024-02, Vol.39 (2), p.227-234
issn 0885-3185
1531-8257
language eng
recordid cdi_proquest_miscellaneous_2928946517
source Wiley
subjects chorea
Chromosome 4
gene
Gene mapping
genetics
history of medicine
Huntingtin
Huntington's disease
Huntingtons disease
Localization
title The Huntington's Disease Gene Discovery
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T10%3A29%3A16IST&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=The%20Huntington's%20Disease%20Gene%20Discovery&rft.jtitle=Movement%20disorders&rft.au=Franklin,%20Gustavo%20L.&rft.date=2024-02&rft.volume=39&rft.issue=2&rft.spage=227&rft.epage=234&rft.pages=227-234&rft.issn=0885-3185&rft.eissn=1531-8257&rft_id=info:doi/10.1002/mds.29703&rft_dat=%3Cproquest_cross%3E2928946517%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3133-eb7622a957174ea82b689e1a4c8f8540f813da7af98280ea9518890658ffdfea3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2932320087&rft_id=info:pmid/38179605&rfr_iscdi=true