07.01.2013 Views

[Abstract Title]. - Society for Neuroscience

[Abstract Title]. - Society for Neuroscience

[Abstract Title]. - Society for Neuroscience

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

Authors: E. CASTRO, J. Y. LAGUNA-TORRES, I. J. SANTOS SOTO, Y. GOENAGA, C.<br />

LAGO, H. G. ORTIZ ZUAZAGA, *S. PENA DE ORTIZ;<br />

Dept Biol, Univ. Puerto Rico, San Juan, Puerto Rico<br />

<strong>Abstract</strong>: We assess here the importance of genomic rearrangement mechanisms in<br />

consolidation of hippocampal dependent learning. Our overarching hypothesis is that long-term<br />

memory <strong>for</strong>mation involves a regulatory mechanism of DNA recombination in the hippocampus<br />

that includes the activation of effector molecules, such as DNA ligases, and the rearrangement of<br />

specific target genes. Using context fear conditioning as a model of learning in C57BL/6 mice,<br />

our main goal is to study genetic changes associated to DNA rearrangements and their impact on<br />

hippocampal dependent memory <strong>for</strong>mation and synaptogenesis. Our previous studies using<br />

pharmacological blockade of DNA ligase function, showed that this treatment specifically<br />

blocked consolidation of context fear conditioning without interfering short-term memory or<br />

reconsolidation (Colón-Cesario et al., 2006). The present studies have determined that similar<br />

treatments block remote memory of context fear conditioning and impair hippocampal<br />

synaptogenesis. These studies are being followed up by experiments aimed at identifying the<br />

genes that are subject to DNA recombination as a result of conditioning. Our results so far<br />

suggest that context fear conditioning results in associative learning-specific changes in<br />

hippocampal gene expression, some of which may be associated to genomic diversification<br />

processes in the brain.<br />

Disclosures: E. Castro, None; J.Y. Laguna-Torres, None; I.J. Santos Soto, None; Y.<br />

Goenaga, None; C. Lago, None; H.G. Ortiz Zuazaga, None; S. Pena de Ortiz , None.<br />

Poster<br />

295. Memory Consolidation, Reconsolidation, Anatomy, and Mechanisms<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 295.24/TT2<br />

Topic: F.02.h. Memory modulation, consolidation, and reconsolidation<br />

Support: NIH<br />

RIKEN<br />

<strong>Title</strong>: Creation of a transgenic mouse line lacking NMDA receptor subunit 1 in layer III<br />

pyramidal neurons of the entorhinal cortex<br />

Authors: A. RIVEST 1 , J. SUH 1,3,4 , *S. TONEGAWA 2,3,4 ;<br />

1 Picower Inst. Memory & Learning, 2 Dir, Picower Inst. Memory & Learning, Massachusetts Inst.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!