The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits Export

@article{citeulike:2651062, abstract = {Methyl-CpG binding proteins (MBDs) are central components of DNA methylation-mediated epigenetic gene regulation. Alterations of epigenetic pathways are known to be associated with several neurodevelopmental disorders, particularly autism. Our previous studies showed that the loss of Mbd1 led to reduced hippocampal neurogenesis and impaired learning in mice. However, whether MBD1 regulates the autism-related cognitive functions remains unknown. Here we show that Mbd1 mutant (Mbd1/) mice exhibit several core deficits frequently associated with autism, including reduced social interaction, learning deficits, anxiety, defective sensory motor gating, depression, and abnormal brain serotonin activity. Furthermore, we find that Mbd1 can directly regulate the expression of Htr2c, one of the serotonin receptors, by binding to its promoter, and the loss of Mbd1 led to elevated expression of Htr2c. Our results therefore demonstrate the importance of epigenetic regulation in mammalian brain development and cognitive functions. Understanding how the loss of Mbd1 could lead to autism-like behavioral phenotypes would reveal much-needed information about the molecular pathogenesis of autism. 10.1093/hmg/ddn102}, author = {Allan, Andrea M. and Liang, Xiaomin and Luo, Yuping and Pak, Changhui and Li, Xuekun and Szulwach, Keith E. and Chen, Dahua and Jin, Peng and Zhao, Xinyu}, citeulike-article-id = {2651062}, citeulike-linkout-0 = {http://dx.doi.org/10.1093/hmg/ddn102}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/18385101}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=18385101}, day = {1}, doi = {10.1093/hmg/ddn102}, journal = {Hum. Mol. Genet.}, keywords = {behavior, disease, epigenetics, mbd, methylation, neuroscience}, month = {April}, pages = {ddn102+}, posted-at = {2008-04-10 22:43:56}, priority = {2}, title = {The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits}, url = {http://dx.doi.org/10.1093/hmg/ddn102}, year = {2008} }

TY - JOUR ID - citeulike:2651062 L3 - citeulike-article-id:2651062 N2 - Methyl-CpG binding proteins (MBDs) are central components of DNA methylation-mediated epigenetic gene regulation. Alterations of epigenetic pathways are known to be associated with several neurodevelopmental disorders, particularly autism. Our previous studies showed that the loss of Mbd1 led to reduced hippocampal neurogenesis and impaired learning in mice. However, whether MBD1 regulates the autism-related cognitive functions remains unknown. Here we show that Mbd1 mutant (Mbd1/) mice exhibit several core deficits frequently associated with autism, including reduced social interaction, learning deficits, anxiety, defective sensory motor gating, depression, and abnormal brain serotonin activity. Furthermore, we find that Mbd1 can directly regulate the expression of Htr2c, one of the serotonin receptors, by binding to its promoter, and the loss of Mbd1 led to elevated expression of Htr2c. Our results therefore demonstrate the importance of epigenetic regulation in mammalian brain development and cognitive functions. Understanding how the loss of Mbd1 could lead to autism-like behavioral phenotypes would reveal much-needed information about the molecular pathogenesis of autism. 10.1093/hmg/ddn102 JF - Hum. Mol. Genet. TI - The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits SP - ddn102 KW - behavior KW - disease KW - epigenetics KW - mbd KW - methylation KW - neuroscience AU - Allan, Andrea AU - Liang, Xiaomin AU - Luo, Yuping AU - Pak, Changhui AU - Li, Xuekun AU - Szulwach, Keith AU - Chen, Dahua AU - Jin, Peng AU - Zhao, Xinyu PY - 2008/04/01/ UR - http://dx.doi.org/10.1093/hmg/ddn102 ER -