Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome

被引:66
作者
Molina, Jessica [1 ,2 ]
Carmona-Mora, Paulina [1 ,2 ]
Chrast, Jacqueline [3 ]
Krall, Paola M. [1 ,2 ]
Canales, Cesar P. [1 ,2 ]
Lupski, James R. [4 ,5 ,6 ]
Reymond, Alexandre [3 ]
Walz, Katherina [1 ]
机构
[1] Ctr Estudios Cient, Ctr Estudios Cientificos, Valdivia, Chile
[2] Univ Austral Chile, Valdivia, Chile
[3] Univ Lausanne, Ctr Integrat Gen, Lausanne, Switzerland
[4] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[6] Texas Childrens Hosp, Houston, TX 77030 USA
关键词
D O I
10.1093/hmg/ddn148
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Potocki-Lupski syndrome (PTLS) is associated with a microduplication of 17p11.2. Clinical features include multiple congenital and neurobehavioral abnormalities and autistic features. We have generated a PTLS mouse model, Dp(11)17/+, that recapitulates some of the physical and neurobehavioral phenotypes present in patients. Here, we investigated the social behavior and gene expression pattern of this mouse model in a pure C57BL/6-Tyr(c-Brd) genetic background. Dp(11)17/+ male mice displayed normal home-cage behavior but increased anxiety and increased dominant behavior in specific tests. A subtle impairment in the preference for a social target versus an inanimate target and abnormal preference for social novelty (the preference to explore an unfamiliar mouse versus a familiar one) was also observed. Our results indicate that these animals could provide a valuable model to identify the specific gene(s) that confer abnormal social behaviors and that map within this delimited genomic deletion interval. In a first attempt to identify candidate genes and for elucidating the mechanisms of regulation of these important phenotypes, we directly assessed the relative transcription of genes within and around this genomic interval. In this mouse model, we found that candidates genes include not only most of the duplicated genes, but also normal-copy genes that flank the engineered interval; both categories of genes showed altered expression levels in the hippocampus of Dp(11)17/+ mice.
引用
收藏
页码:2486 / 2495
页数:10
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