Reversible phosphorylation processes in cell cycle control: role of Cdc14 protein phosphatases
Centro de Investigación del Cáncer (Universidad de Salamanca-CSIC)
Campus Universitario Miguel de Unamuno s/n
37007 Salamanca
SPAIN
Fundación Solórzano (2013-2013)
Estudio de Cdc14B en el mantenimiento de la estabilidad genómica: análisis de sus interacciones proteicas.
MINISTERIO DE CIENCIA E INNOVACION (2009-2011)
Mecanismos de regulacion de la mitosis en celulas humanas: implicacion de las fosfatasas CDC14
Junta de Castilla y León (2008-2008)
“Mecanismos de regulación de las fosfatasa cdc14 humanas a lo largo del ciclo de división celular”
Fundación Solórzano (2008-2008)
Mecanismos de regulación de las fosfatasas Cdc14 humanas a lo largo del Ciclo de División Celular.
Junta de Castilla y León (2007-2007)
Estudio de las fosfatasas CDC 14 humanas y su particiopación el¡n la regulacion de procesos mitóticos.
MINISTERIO DE EDUCACION Y CIENCIA (2005-2008)
Estudio de las fosfatasas cdc14 en la regulacion de la salida de mitosis en células humanas
MINISTERIO DE CIENCIA Y TECNOLOGIA (2002-2005)
Estudio de los mecanismos de regulación de la salida de mitosis en células humanas
(*) Means equal contribution as senior authors.
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Macarena Alcalá Domínguez
Esmeralda Alonso Rodríguez
Andrés Avelino Bueno Núñez
Genetic stability: Genome replication and DNA damage tolerance
Telf.:
Fax:
Email: abn@usal.es
Dr. Avelino Bueno Núñez
Catedrático de Microbiología.
Laboratorio Nº 5
923 294 805
abn(arroba)usal(.)es
Centro de Investigación del Cáncer (Universidad de Salamanca-CSIC)
Campus Universitario Miguel de Unamuno s/n
37007 Salamanca
SPAIN
Avelino Bueno received his Ph.D. from the Department of Microbiology at the University of Salamanca (USAL, Spain) in 1988 thanks to the support of a PFPI fellowship from the Spanish Ministry of Science and Education. His doctoral dissertation summarized the molecular characterization of genes encoding exocellular carbohydrolases from Bacillus species, a scientific project run under the supervision of Professors Francisco del Rey, Julio Rodriguez-Villanueva and Tomás González-Villa.
From 1989 to 1991, he carried out postdoctoral training in the cell cycle field in Dr. Paul Russell’s group at the Scripps Research Foundation in La Jolla (California) thanks to the support of a Fulbright Posdoctoral Fellowship. He remained there as a senior postdoc until the end of 1992 as a R+D employee of The Scripps Research Institute (TSRI). During this period of time he characterized genes involved in cell cycle regulation encoding key proteins such as the DNA replication initiator Cdc6, the G2/M kinase Swe1, and those encoding G2 and G1 cyclins Cig1 and Cig2 in yeast models (Cell 1991, EMBO Journal 1992, Mol Cell Biol 1993 and J Biol Chem 1994). Avelino Bueno developed at TSRI a strong interest in DNA replication control mechanisms in the cell cycle field before starting his own research group at the beginning of 1993.
Avelino Bueno formed his own lab at the University of Salamanca with a clear focus on specific DNA replication control mechanisms involving the initiator protein Cdc6/Cdc18, the Rad53/Chk2 checkpoint kinase, as well as phosphatases Cdc14/Flp1, using as experimental models both budding and fission yeast (JBC 99, JCS 99, JBC, 00, Nature 01, JCS 01 and 04, Genes&Dev 05, NARes 06, MBC 08), later to expand to cell cycle phosphatases Cdc14A and Cdc14B in animal cell models in collaboration with Dr. María Sacristán (JBC 05, CC 06/08/11, JBC 10, MBC 12, SR, under review). Initially (1993-2000) his group was first established at the IMB Research Institute (USAL-CSIC) thanks to a tenured associated professorship position to later move to the Cancer Research Institute (IMBCC USAL-CSIC), in 2001, as a full professor of Microbiology. In the last seven years his lab has been particularly interested in the mechanism reverting PCNA ubiquitylation. In particular, his research team has been focused in understanding the biological meaning of PCNA deubiquitylation during S-phase to uncover the consequences of altering this evolutionarily conserved eukaryotic mechanism (BST 10, PLoS Genetics 12, PLoS ONE 13, Scientific Reports 16).
It is important to mention that throughout the years, Dr. Bueno has establshed productive scientific collaborations with Spanish and International Research Groups (i.e.: Sergio Moreno, IBMCC; Pedro San Segundo, IBFG; Rodrigo Bermejo, CIB; Viesturs Simanis, ISREC-Lausanne; Karim Labib, Dundee University; Luis Aragón, MRC-London). Finally, it is also noteworthy to acknowledge that, from 2012 to 2016, Dr. Bueno has been Director/Coordinator of the Master Degree in Biology and Clinic of Cancer, official title of the University of Salamanca, a key part of the Postgraduate School of the Cancer Research Institute in Salamanca (IMBCC USAL-CSIC)
1984-1988 PhD studies. Department of Microbiology, University of Salamanca. IMB, joint research center CSIC/University of Salamanca.
1989-1992 Post-doctoral Fulbright Fellow in Paul Russell’s lab (Department of Molecular Biology) at “The Scripps Research Institute” in La Jolla, California (USA).
1993-2002 Assistant Professor of Microbiology, University of Salamanca. Member of IMB, joint research center CSIC/University of Salamanca.
2002-present. Professor of Microbiology, Department of Microbiology and Genetics, University of Salamanca. Member of IBMCC at the Cancer Research Center of the University of Salamanca.
× Manuel Jacob Fuentes Matos
Manuel Jacob Fuentes Matos
Vidal Garzón Díaz
Sofía Hernández Luelmo
Marcos Manrique Crespo
Lucía Rodríguez González
Sergio Rodríguez Pérez
María de la Paz Sacristán Martín
Reversible phosphorylation processes in cell cycle control: role of Cdc14 protein phosphatases
Telf.:
Fax:
Email: msacristan@usal.es
José Luis Torbado Gardeazábal
Dayra Valencia Sánchez
Javier Zamarreño Lozano
Laura Ahumada Arranz
Vanesa Álvarez Álvarez
Violeta Cordón Preciado
Helena Diaz Cuervo
Verónica Esteban Martín
Alfonso Gallego Sánchez
Juan Antonio Canete de la Calle
Saúl Martín Sánchez
Sofía Muñoz Félix
Sara Ovejero Merino
Sandra Ufano Ortiz
