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发育中丘脑候选连接标签的双策略表达筛选

A dual-strategy expression screen for candidate connectivity labels in the developing thalamus.

作者信息

Bibollet-Bahena Olivia, Okafuji Tatsuya, Hokamp Karsten, Tear Guy, Mitchell Kevin J

机构信息

Smurfit Institute of Genetics, Trinity College Dublin, Dublin, Ireland.

Department of Developmental Neurobiology, New Hunt's House, Guy's Campus, King's College, London, United Kingdom.

出版信息

PLoS One. 2017 May 30;12(5):e0177977. doi: 10.1371/journal.pone.0177977. eCollection 2017.

Abstract

The thalamus or "inner chamber" of the brain is divided into ~30 discrete nuclei, with highly specific patterns of afferent and efferent connectivity. To identify genes that may direct these patterns of connectivity, we used two strategies. First, we used a bioinformatics pipeline to survey the predicted proteomes of nematode, fruitfly, mouse and human for extracellular proteins containing any of a list of motifs found in known guidance or connectivity molecules. Second, we performed clustering analyses on the Allen Developing Mouse Brain Atlas data to identify genes encoding surface proteins expressed with temporal profiles similar to known guidance or connectivity molecules. In both cases, we then screened the resultant genes for selective expression patterns in the developing thalamus. These approaches identified 82 candidate connectivity labels in the developing thalamus. These molecules include many members of the Ephrin, Eph-receptor, cadherin, protocadherin, semaphorin, plexin, Odz/teneurin, Neto, cerebellin, calsyntenin and Netrin-G families, as well as diverse members of the immunoglobulin (Ig) and leucine-rich receptor (LRR) superfamilies, receptor tyrosine kinases and phosphatases, a variety of growth factors and receptors, and a large number of miscellaneous membrane-associated or secreted proteins not previously implicated in axonal guidance or neuronal connectivity. The diversity of their expression patterns indicates that thalamic nuclei are highly differentiated from each other, with each one displaying a unique repertoire of these molecules, consistent with a combinatorial logic to the specification of thalamic connectivity.

摘要

大脑的丘脑或“内室”被分为约30个离散的核团,具有高度特异的传入和传出连接模式。为了鉴定可能指导这些连接模式的基因,我们采用了两种策略。首先,我们使用一个生物信息学流程,在线虫、果蝇、小鼠和人类的预测蛋白质组中,搜索包含在已知导向或连接分子中发现的任何一种基序的细胞外蛋白质。其次,我们对艾伦发育中小鼠脑图谱数据进行聚类分析,以鉴定编码表面蛋白的基因,这些表面蛋白的表达时间模式与已知导向或连接分子相似。在这两种情况下,我们随后筛选所得基因在发育中的丘脑中的选择性表达模式。这些方法在发育中的丘脑中鉴定出82个候选连接标记。这些分子包括许多 Ephrin、Eph 受体、钙黏蛋白、原钙黏蛋白、信号素、丛状蛋白、Odz/teneurin、Neto、小脑素、钙联蛋白和 Netrin-G 家族的成员,以及免疫球蛋白(Ig)和富含亮氨酸受体(LRR)超家族的不同成员、受体酪氨酸激酶和磷酸酶、多种生长因子和受体,以及大量以前未涉及轴突导向或神经元连接的杂项膜相关或分泌蛋白。它们表达模式的多样性表明丘脑核团彼此高度分化,每个核团都展示了这些分子的独特组合,这与丘脑连接特异性的组合逻辑一致。

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