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在发育过程中,小脑颗粒神经元前体细胞中Chrnα3的限制性表达需要Pax6对Tlx3进行调控。

Regulation of Tlx3 by Pax6 is required for the restricted expression of Chrnα3 in Cerebellar Granule Neuron progenitors during development.

作者信息

Divya Thulasi Sheela, Lalitha Soundararajan, Parvathy Surendran, Subashini Chandramohan, Sanalkumar Rajendran, Dhanesh Sivadasan Bindu, Rasheed Vazhanthodi Abdul, Divya Mundackal Sivaraman, Tole Shubha, James Jackson

机构信息

Neuro Stem Cell Biology Laboratory, Neurobiology Division, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala-695 014, India.

Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai-400005, India.

出版信息

Sci Rep. 2016 Jul 25;6:30337. doi: 10.1038/srep30337.

Abstract

Homeobox gene Tlx3 is known to promote glutamatergic differentiation and is expressed in post-mitotic neurons of CNS. Contrary to this here, we discovered that Tlx3 is expressed in the proliferating progenitors of the external granule layer in the cerebellum, and examined factors that regulate this expression. Using Pax6(-/-)Sey mouse model and molecular interaction studies we demonstrate Pax6 is a key activator of Tlx3 specifically in cerebellum, and induces its expression starting at embryonic day (E)15. By Postnatal day (PN)7, Tlx3 is expressed in a highly restricted manner in the cerebellar granule neurons of the posterior cerebellar lobes, where it is required for the restricted expression of nicotinic cholinergic receptor-α3 subunit (Chrnα3) and other genes involved in formation of synaptic connections and neuronal migration. These results demonstrate a novel role for Tlx3 and indicate that Pax6-Tlx3 expression and interaction is part of a region specific regulatory network in cerebellum and its deregulation during development could possibly lead to Autistic spectral disorders (ASD).

摘要

已知同源框基因Tlx3可促进谷氨酸能分化,并在中枢神经系统的有丝分裂后神经元中表达。与此相反,我们在此发现Tlx3在小脑外颗粒层的增殖祖细胞中表达,并研究了调节这种表达的因素。利用Pax6(-/-)Sey小鼠模型和分子相互作用研究,我们证明Pax6是Tlx3在小脑中的关键激活因子,并在胚胎第15天(E15)开始诱导其表达。到出生后第7天(PN7),Tlx3在后小脑叶的小脑颗粒神经元中以高度受限的方式表达,在那里它是烟碱型胆碱能受体α3亚基(Chrnα3)和其他参与突触连接形成和神经元迁移的基因受限表达所必需的。这些结果证明了Tlx3的新作用,并表明Pax6-Tlx3的表达和相互作用是小脑中区域特异性调节网络的一部分,其在发育过程中的失调可能导致自闭症谱系障碍(ASD)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/234b/4959012/0c3d44544505/srep30337-f1.jpg

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