<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-05T22:06:32Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/64454" metadataPrefix="didl">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/64454</identifier><datestamp>2026-04-09T10:27:04Z</datestamp><setSpec>com_10324_1134</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1213</setSpec></header><metadata><d:DIDL xmlns:d="urn:mpeg:mpeg21:2002:02-DIDL-NS" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="urn:mpeg:mpeg21:2002:02-DIDL-NS http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/did/didl.xsd">
<d:DIDLInfo>
<dcterms:created xmlns:dcterms="http://purl.org/dc/terms/" xsi:schemaLocation="http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/dcterms.xsd">2024-01-11T12:40:12Z</dcterms:created>
</d:DIDLInfo>
<d:Item id="hdl_10324_64454">
<d:Descriptor>
<d:Statement mimeType="application/xml; charset=utf-8">
<dii:Identifier xmlns:dii="urn:mpeg:mpeg21:2002:01-DII-NS" xsi:schemaLocation="urn:mpeg:mpeg21:2002:01-DII-NS http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/dii/dii.xsd">urn:hdl:10324/64454</dii:Identifier>
</d:Statement>
</d:Descriptor>
<d:Descriptor>
<d:Statement mimeType="application/xml; charset=utf-8">
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins</dc:title>
<dc:creator>Infante Sanz, María Del Mar</dc:creator>
<dc:creator>Duran Dominguez, María Mercedes</dc:creator>
<dc:creator>Acedo, Alberto</dc:creator>
<dc:creator>Sánchez Tapia, Eva María</dc:creator>
<dc:creator>Díez Gómez, Beatríz</dc:creator>
<dc:creator>Barroso, Alicia</dc:creator>
<dc:creator>García González, María</dc:creator>
<dc:creator>Feliubadalo, L.</dc:creator>
<dc:creator>Lasa, Adriana</dc:creator>
<dc:creator>Hoya, Miguel de la</dc:creator>
<dc:creator>Esteban Cardeñosa, Eva</dc:creator>
<dc:creator>Diez, Orland</dc:creator>
<dc:creator>Martinez Bouzas, Cristina</dc:creator>
<dc:creator>Godino, Javier</dc:creator>
<dc:creator>Teulé, Alexandra</dc:creator>
<dc:creator>Osorio, Ana</dc:creator>
<dc:creator>Lastra, Enrique</dc:creator>
<dc:creator>González  Sarmiento, Rogelio</dc:creator>
<dc:creator>Miner, Cristina</dc:creator>
<dc:creator>Velasco, Eladio A.</dc:creator>
<dc:description>BRCA2-c.2808_2811del (3036delACAA) is one of the most reported&#xd;
germ line mutations in non-Ashkenazi breast cancer patients. We&#xd;
investigated its genetic origin in 51 Spanish carrier families that&#xd;
were genotyped with 11 13q polymorphic markers. Three independent&#xd;
associated haplotypes were clearly distinguished accounting for&#xd;
23 [west Castilla y León (WCL)], 20 [east Castilla y León (ECL)]&#xd;
and 6 (South of Spain) families. Mutation age was estimated with&#xd;
the Disequilibrium Mapping using Likelihood Estimation software&#xd;
in a range of 45–68 and 45–71 generations for WCL and ECL haplotypes,&#xd;
respectively. The most prevalent variants, c.2808_2811del&#xd;
and c.2803G > A, were located in a double-hairpin loop structure&#xd;
(c.2794–c.2825) predicted by Quikfold that was proposed as a mutational&#xd;
hotspot. To check this hypothesis, random mutagenesis was&#xd;
performed over a 923 bp fragment of BRCA2, and 86 DNA variants&#xd;
were characterized. Interestingly, three mutations reported in the&#xd;
mutation databases (c.2680G > A, c.2944del and c.2957dup) were&#xd;
replicated and 20 affected the same position with different nucleotide&#xd;
changes. Moreover, five variants were placed in the same hairpin loop&#xd;
of c.2808_2811del, and one affected the same position (c.2808A > G).&#xd;
In conclusion, our results support that at least three different mutational&#xd;
events occurred to generate c.2808_2811del. Other highly&#xd;
prevalent DNA variants, such as BRCA1-c.68_69delAG, BRCA2-&#xd;
c.5946delT and c.8537delAG, are concentrated in hairpin loops, suggesting&#xd;
that these structures may represent mutational hotspots.</dc:description>
<dc:date>2024-01-11T12:40:12Z</dc:date>
<dc:date>2024-01-11T12:40:12Z</dc:date>
<dc:date>2013</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Carcinogenesis, 34 (11), pp. 2505-2511.</dc:identifier>
<dc:identifier>0143-3334</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/64454</dc:identifier>
<dc:identifier>10.1093/carcin/bgt272</dc:identifier>
<dc:identifier>2505</dc:identifier>
<dc:identifier>11</dc:identifier>
<dc:identifier>2511</dc:identifier>
<dc:identifier>Carcinogenesis</dc:identifier>
<dc:identifier>34</dc:identifier>
<dc:identifier>1460-2180</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>http://dx.doi.org/10.1093/carcin/bgt272</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>Oxford University Press</dc:publisher>
</oai_dc:dc>
</d:Statement>
</d:Descriptor>
<d:Component id="10324_64454_1">
<d:Resource ref="https://uvadoc.uva.es/bitstream/10324/64454/1/Carcinogenesis-2013-Infante-2808del.pdf" mimeType="application/pdf"/>
</d:Component>
</d:Item>
</d:DIDL></metadata></record></GetRecord></OAI-PMH>