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   <dc:title>In vivo conditional deletion of HDAC7 reveals its requirement to establish proper B lymphocyte identity and development</dc:title>
   <dc:creator>Azagra Rodríguez, Alba</dc:creator>
   <dc:creator>Román González, Lidia</dc:creator>
   <dc:creator>Collazo, Olga</dc:creator>
   <dc:creator>Rodríguez Ubreva, Javier</dc:creator>
   <dc:creator>Yébenes, Virginia G. de</dc:creator>
   <dc:creator>Barneda Zahonero, Bruna</dc:creator>
   <dc:creator>Rodríguez Lumbiarres, Jairo, 1980-</dc:creator>
   <dc:creator>Castro de Moura, Manuel</dc:creator>
   <dc:creator>Grego Bessa, Joaquim</dc:creator>
   <dc:creator>Fernández Duran, Irene</dc:creator>
   <dc:creator>Islam, Abul B. M. M. K.</dc:creator>
   <dc:creator>Esteller, Manel</dc:creator>
   <dc:creator>Ramiro, Almudena R.</dc:creator>
   <dc:creator>Ballestar Tarín, Esteban</dc:creator>
   <dc:creator>Parra Bola, Mª Isabel</dc:creator>
   <dc:subject>Cèl·lules B</dc:subject>
   <dc:subject>Histones</dc:subject>
   <dc:subject>Limfòcits</dc:subject>
   <dc:subject>Gens</dc:subject>
   <dc:subject>Proteïnes</dc:subject>
   <dc:subject>B cells</dc:subject>
   <dc:subject>Histones</dc:subject>
   <dc:subject>Lymphocytes</dc:subject>
   <dc:subject>Genes</dc:subject>
   <dc:subject>Proteins</dc:subject>
   <dc:description>Class IIa histone deacetylase (HDAC) subfamily members are tissue-specific gene repressors with crucial roles in development and differentiation processes. A prominent example is HDAC7, a class IIa HDAC that shows a lymphoid-specific expression pattern within the hematopoietic system. In this study, we explored its potential role in B cell development by generating a conditional knockout mouse model. Our study demonstrates for the first time that HDAC7 deletion dramatically blocks early B cell development and gives rise to a severe lymphopenia in peripheral organs, while also leading to pro-B cell lineage promiscuity. We find that HDAC7 represses myeloid and T lymphocyte genes in B cell progenitors through interaction with myocyte enhancer factor 2C (MEFC2). In B cell progenitors, HDAC7 is recruited to promoters and enhancers of target genes, and its absence leads to increased enrichment of histone active marks. Our results prove that HDAC7 is a bona fide transcriptional repressor essential for B cell development.</dc:description>
   <dc:date>2017-05-16T13:17:50Z</dc:date>
   <dc:date>2017-05-30T22:01:30Z</dc:date>
   <dc:date>2016-11</dc:date>
   <dc:date>2017-05-16T13:17:50Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>0022-1007</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/111110</dc:identifier>
   <dc:identifier>669675</dc:identifier>
   <dc:identifier>27810920</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1084/jem.20150821</dc:relation>
   <dc:relation>Journal of Experimental Medicine, 2016, vol. 213, num. 12, p. 2591-2601</dc:relation>
   <dc:relation>https://doi.org/10.1084/jem.20150821</dc:relation>
   <dc:rights>(c) Rockefeller University Press, 2016</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>11 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Rockefeller University Press</dc:publisher>
   <dc:source>Articles publicats en revistes (Ciències Fisiològiques)</dc:source>
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