Gene Regulation, Stem Cells and Cancer
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1990 PhD Centro de Biología Molecular, Universidad Autónoma de Madrid (Spain)
1991-1995 Postdoctoral work at the University of Massachusetts.
1996-2002 Group Leader at the European Molecular Biology Laboratory.
June 2002 ICREA Research Professor and Group Leader at the Centre de Regulació Genòmica, Barcelona (Spain)
2012 Coordinator of the Gene Regulation, Stem Cells and Cancer Programme, Centre de Regulació Genòmica, Barcelona (Spain)
Jordi Hernández awarded the CERCA Pioner Prize 2017 (21/12/2017)
Jordi Hernández, former PhD student at Juan Valcárcel’s laboratory and current CRG Entrepreneur in Residence has been awarded the CERCA Pioneer Prize. The CERCA Pioneer Awards recognise those researchers who have presented a doctoral thesis with results that are clearly aimed at commercial exploitation.
CaixaImpulse funds a project to develop a new cancer treatment based in aternative splicing (01/08/2017)
Jordi Hernández, researcher at Juan Valcárcel’s laboratory and young entrepreneur participating in the CRG Entrepreneur-in-Residence programme, will lead this innovative project.
The good, the bad and the spliceosome! (26/11/2016)
The Fas protein can either inhibit or promote the controlled cell death (apoptosis), depending on the isoform in which it occurs. Researchers from the Helmholtz Zentrum München, the Technical University of Munich, and the Centre for Genomic Regulation in Barcelona, in collaboration with the Institute of Molecular Genetics of Montpeller, have elucidated how this decision is guided.
Juan Valcárcel elected President of the RNA Society (14/06/2016)
Juan Valcárcel, coordinator of the Gene Regulation, Stem Cells and Cancer Programme and ICREA research professor at the CRG, has been elected President of the RNA Society for 2017-2018. The RNA Society Board just announced the election of Prof Valcarcel this week, and that Kathleen Hall, Haruhiko Siomi, and Chris Smith were chosen to be Members of the Board for that same period.
The genome provides the instructions to build and maintain the function of a living organism. Strangely, in complex organisms these instructions are not written as continuous messages, but rather as smaller pieces (known as exons) interrupted by meaningless text (known as introns). This arrangement has the advantage that the pieces can be combined in different ways to generate alternative instructions, a mechanism that cells utilize to expand the information content of their genomes.
We study the complex molecular machinery that in the cell nucleus removes introns from the primary transcripts of genes, a process known as pre-mRNA splicing. We are particularly interested in how splicing is regulated to generate alternative mRNAs, a process used by the majority of human genes to generate proteins with different, even antagonistic functions. Alternative splicing is regulated during cell differentiation and development, and contributes to the normal physiology of multicellular organisms. Alterations in the splicing process are also a frequent cause of genetic diseases and contribute to common pathologies, including cancer.