Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/163924
Share/Export:
logo share SHARE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Title

Uncovering p63 targets involved in hereditary malformations

AuthorsTena, Juan J. CSIC ORCID; Santos Pereira, J. M.; Acemel, Rafael D.; Gómez-Skarmeta, José Luis CSIC ORCID
Issue Date2017
CitationFEBS3+ (2017)
XL SEBBM Congress (2017)
Abstractp63 transcription factor plays an important role during epidermis and neural crest derivatives formation. Mutations affecting its coding sequence or its target genes lead to the development of malformations mainly characterized by cleft palate, ectodermal dysplasia and limb malformation. To date, the search of genetic events underlying these malformations has been mainly focused on exonic regions. However, impairment on the transcriptional regulation of genes related to these phenotypes might cause similar diseases. The major problem of the studies focused on transcription factors binding sites is the difficulty to associate a certain regulatory region with its target gene. In general, this association is solely established having into account the proximity between these elements, which might lead to wrong assignments and waste of effort and resources in deeply studying the incorrect genes. To overcome this problem, we designed an approach based on binding sites and chromatin 3D interactions, which will allow us to properly associate transcriptional regulatory elements with their target genes. First, we performed a ChIP-seq in zebrafish to find p63 binding sites, and then 4C-seq experiments centered in some of these putative regulatory regions to uncover their regulatory landscape. Finally, we moved to genome-wide scale by means of a novel technique, the HiChIP, which allowed us to obtain a global map of contacts from every active promoter and assign the most probable target gene to each binding site. The integration of these data will provide us a list of genes contacting p63-binding regions, which could potentially belong to the p63 genetic network and be involved in p63-related diseases.
DescriptionResumen del póster presentado al 1st Joint Meeting of the French-Portuguese-Spanish Biochemical and Molecular Biology Societies y al XL Spanish Society of Biochemistry and Molecular Biology (SEBBM) Congress, celebrado en Barcelona (España) del 23 al 26 de octubre de 2017.
URIhttp://hdl.handle.net/10261/163924
Appears in Collections:(CABD) Comunicaciones congresos

Files in This Item:
File Description SizeFormat
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work

Google ScholarTM

Check


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.