Autism Spectrum Disorder Genes: Disease-Related Networks and Compensatory Strategies

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15

초록

The mammalian brain comprises structurally and functionally distinct regions. Each of these regions has characteristic molecular mechanisms that mediate higher-order tasks, such as memory, learning, emotion, impulse, and motor control. Many genes are involved in neuronal signaling and contribute to normal brain development. Dysfunction of essential components of neural signals leads to various types of brain disorders. Autism spectrum disorder is a neurodevelopmental disorder characterized by social deficits, communication challenges, and compulsive repetitive behaviors. Long-term genetic studies have uncovered key genes associated with autism spectrum disorder, such as SH3 and multiple ankyrin repeat domains 3, methyl-CpG binding protein 2, neurexin 1, and chromodomain helicase DNA binding protein 8. In addition, disease-associated networks have been identified using animal models, and the understanding of the impact of these genes on disease susceptibility and compensation is deepening. In this review, we examine rescue strategies using key models of autism spectrum disorder.

키워드

autism spectrum disordergenetic mice modelpathophysiologypharmacological restorationgenetic restorationSCAFFOLDING PROTEIN SHANK3RETT-SYNDROMEMOUSE MODELSYNAPTIC PLASTICITYRODENT MODELSNEUREXIN SUPERFAMILYEXCITATORY SYNAPSESNEUROTROPHIC FACTORMECP2 DEFICIENCYMUTANT MICE
제목
Autism Spectrum Disorder Genes: Disease-Related Networks and Compensatory Strategies
저자
Yoon, Jong HyukSong, MinseokLim, Hye Kyung
DOI
10.3389/fnmol.2022.922840
발행일
2022-06
저널명
Frontiers in Molecular Neuroscience
15