[ES]En comparación con los ratones de control WT, los ratones Pttg1 KO aprendieron a resolver la tarea de una manera menos eficiente, lo que sugiere problemas en la consolidación de la memoria. El rendimiento de los ratones KO para RasGrf1 fue similar al de los controles y aprendieron a utilizar la mejor estrategia de búsqueda. Los ratones Doble KO alcanzaron un mejor nivel de aprendizaje espacial que WT. Conclusión: Se sugiere un papel para Pttg1 en la consolidación/formación de la memoria, mientras que Nuestros ratones RasGrf1 KO no muestran defectos de memoria asociados al hipocampo.
[EN]Background: RasGrf1 is a guanine-nucleotide releasing factor that enhances Ras activity. Human PTTG1 is an oncoprotein found in pituitary tumors and later identified
as securin, a protein isolated from yeast with a reported role in chromosome separation. It has been suggested that RasGrf1 is an important upstream component of
signal transduction pathways regulating Pttg1 expression and controlling beta cell
development and their physiological response. At memory formation level, there are
contradictory data regarding the role of RasGrf1, while Pttg1 has not been previously studied. Both proteins are expressed in the mammalian hippocampus, which is
one of the key brain areas for spatial learning and memory.
Objective: The aim of this work was to study a potential link between RasGrf1 and
Pttg1 in memory formation.
Method: Spatial learning and memory test in the Pttg1 KO, RasGrf1 KO, and Pttg1-
RasGrf1 double KO and their correspondent WT mice using a Barnes maze.
Results: In comparison with the WT control mice, Pttg1 KO mice learned how to solve
the task in a less efficient way, suggesting problems in memory consolidation. RasGrf1
KO mice performance was similar to controls, and they learned to use the best searching strategy. Double KO mice reached a better spatial learning level than WT.
Conclusion: A role for Pttg1 in memory consolidation/formation is suggested, while
our RasGrf1 KO mice do not show hippocampus associated memory defects.
