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基因与社会环境之间的复杂相互作用导致与自闭症谱系障碍相关的表型出现在小鼠中。

Complex Interactions between Genes and Social Environment Cause Phenotypes Associated with Autism Spectrum Disorders in Mice.

机构信息

School of Biosciences, Cardiff University, Cardiff CF10 3AX, United Kingdom

School of Biosciences, Cardiff University, Cardiff CF10 3AX, United Kingdom.

出版信息

eNeuro. 2020 Aug 10;7(4). doi: 10.1523/ENEURO.0124-20.2020. Print 2020 Jul/Aug.

DOI:10.1523/ENEURO.0124-20.2020
PMID:32669345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7418534/
Abstract

The etiology of autism spectrum disorders (ASDs) is a complex combination of genetic and environmental factors. Neuroligin3, a synaptic adhesion protein, and cytoplasmic interacting protein 1 (CYFIP1), a regulator of protein translation and actin polymerization, are two proteins associated with ASDs that interact in neurons Here, we investigated the role of the Neuroligin3/CYFIP1 pathway in behavioral functioning and synapse formation in mice and found that it contributes to motor learning and synapse formation in males. Similar investigation in female mice revealed an absence of such phenotypes, suggesting that females are protected against mutations affecting this pathway. Previously, we showed that the social environment influences the behavior of male mice. We extended this finding and found that the transcriptome of wild-type mice housed with their mutant littermates, lacking Neuroligin3, differed from the transcriptome of wild-type mice housed together. Altogether, these results identify the role of the Neuroligin3/CYFIP1 pathway in male mouse behavior and highlight its sensitivity to social environment.

摘要

自闭症谱系障碍 (ASD) 的病因是遗传和环境因素的复杂组合。神经黏附素 3 (Neuroligin3) 是一种突触黏附蛋白,细胞质相互作用蛋白 1 (CYFIP1) 是一种蛋白质翻译和肌动蛋白聚合的调节剂,这两种蛋白都与 ASD 有关,在神经元中相互作用。在这里,我们研究了 Neuroligin3/CYFIP1 途径在雄性小鼠行为功能和突触形成中的作用,发现它有助于运动学习和突触形成。在雌性小鼠中的类似研究表明不存在这种表型,表明女性受到保护,免受影响该途径的突变的影响。此前,我们表明社会环境会影响雄性小鼠的行为。我们扩展了这一发现,发现与野生型小鼠一起饲养的、缺乏 Neuroligin3 的突变体同窝仔鼠的转录组与野生型小鼠的转录组不同。总之,这些结果确定了 Neuroligin3/CYFIP1 途径在雄性小鼠行为中的作用,并强调了其对社会环境的敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/b55ae93e17d1/SN-ENUJ200182F007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/79579dc4cbee/SN-ENUJ200182F001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/a2d3d5ea8709/SN-ENUJ200182F003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/6d3fa12f1adb/SN-ENUJ200182F004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/a19436e0049d/SN-ENUJ200182F005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/90e46790dec0/SN-ENUJ200182F006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/b55ae93e17d1/SN-ENUJ200182F007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/79579dc4cbee/SN-ENUJ200182F001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/2f2c2da931a1/SN-ENUJ200182F002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/a2d3d5ea8709/SN-ENUJ200182F003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/6d3fa12f1adb/SN-ENUJ200182F004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/a19436e0049d/SN-ENUJ200182F005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/90e46790dec0/SN-ENUJ200182F006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/312b/7418534/b55ae93e17d1/SN-ENUJ200182F007.jpg

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