首页> 外文期刊>Neurology International >Identification of 17 Highly Expressed Genes within Mouse Lumbar Spinal Cord Anterior Horn Region from an In-Situ Hybridization Atlas of 3430 Genes: Implications for Motor Neuron Disease
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Identification of 17 Highly Expressed Genes within Mouse Lumbar Spinal Cord Anterior Horn Region from an In-Situ Hybridization Atlas of 3430 Genes: Implications for Motor Neuron Disease

机译:从3430基因的原位杂交图集的小鼠腰脊髓前角区域内的17个高表达基因的鉴定:对运动神经元疾病的影响。

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In an effort to find possible new gene candidates involved in the causation of amyotrophic lateral sclerosis (ALS), a prior version of the on-line brain gene expression atlas GENSAT was extensively searched for selectively intense expression within spinal motor neurons. Using autoradiographic data of in-situ hybridization from 3430 genes, a search for selectively intense activity was made for the anterior horn region of murine lumbar spinal cord sectioned in the axial plane. Of 3430 genes, a group of 17 genes was found to be highly expressed within the anterior horn suggesting localization to its primary cellular constituent, the alpha spinal motor neuron. For some genes, an inter-relationship to ALS was already known, such as for heavy, medium, and light neurofilaments, and peripherin. Other genes identified include: Gamma Synuclein, GDNF, SEMA3A, Extended Synaptotagmin-like protein 1, LYNX1, HSPA12a, Cadherin 22, PRKACA, TPPP3 as well as Choline Acetyltransferase, Janus Kinase 1, and the Motor Neuron and Pancreas Homeobox 1. Based on this study, Fibroblast Growth Factor 1 was found to have a particularly selective and intense localization pattern to the ventral horn and may be a good target for development of motor neuron disease therapies; further research is needed.Key words: gene, amyotrophic lateral sclerosis, motor neuron, spinal cord
机译:为了寻找可能与肌萎缩性侧索硬化症(ALS)起因有关的新基因候选者,广泛搜索了在线大脑基因表达图谱GENSAT的先前版本,以寻找脊髓运动神经元内的选择性强表达。使用来自3430个基因的原位杂交放射自显影数据,寻找在轴向平面上切开的鼠腰脊髓前角区域的选择性强烈活性。在3430个基因中,发现有17个基因在前角内高表达,这表明它定位于其主要细胞成分即α脊髓运动神经元。对于某些基因,与ALS的相互关系是已知的,例如重,中,轻神经丝和外周蛋白。确定的其他基因包括:γ突触核蛋白,GDNF,SEMA3A,突触突触素样蛋白1,LYNX1,HSPA12a,钙黏着蛋白22,PRKACA,TPPP3以及胆碱乙酰基转移酶,Janus激酶1和运动神经元和胰腺同源异型盒1。这项研究发现,成纤维细胞生长因子1对腹角具有特别选择性和强烈的定位模式,可能是发展运动神经元疾病疗法的良好靶点。关键词:基因;肌萎缩性侧索硬化;运动神经元;脊髓

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