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首页> 外文期刊>The international journal of developmental biology >Characterization of Hypoxia induced gene 1: Expression during rat Central Nervous System maturation and evidence of antisense RNA expression
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Characterization of Hypoxia induced gene 1: Expression during rat Central Nervous System maturation and evidence of antisense RNA expression

机译:低氧诱导基因1的表征:大鼠中枢神经系统成熟过程中的表达和反义RNA表达的证据

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Although recent studies have provided a detailed understanding of cellular interactions occurring during the development of the CNS, little is known about the molecular signals which during the peri and postnatal periods ensure its maturation and functionality. Using the mammalian spinal cord as a model, we have designed experiments to examine the main changes in gene expression occurring during this critical transition. In this paper we describe the cloning and characterization of the rat hypoxia induced gene-1 (Hig-1), its expression pattern during spinal cord maturation and in situ localization of its mRNA. We show an increase in Hig-1 expression between P1 and P15 in the spinal cord and a differential spatial pattern. In the P1 spinal cord we observed preferential expression in regions of dorsal laminae 11 and III and laminae IX ventrally; while in P8, the distribution was more widespread and overall expression was increased. Hig-1 is also widely expressed in the brain. Results of in situ hybridization experiments, as well as particular features concerning ESTs, led us to propose the expression of an antisense mRNA. Primer-specific RT-PCR demonstrates the presence of this a Hig-1 transcript whose structure has not yet been characterized. The high homology between putative rHig-1 protein and human- and murine-predicted sequences, as well as its characteristic expression in the Central Nervous System, are indicative of a specific role which could be related to apoptosis signaling during postnatal maturation.
机译:尽管最近的研究提供了对中枢神经系统发育过程中发生的细胞相互作用的详细了解,但对分子信号知之甚少,这些分子信号在围产期和产后确保其成熟和功能。以哺乳动物的脊髓为模型,我们设计了实验来检查在这一关键过渡过程中发生的基因表达的主要变化。在本文中,我们描述了大鼠缺氧诱导基因1(Hig-1)的克隆和特征,其在脊髓成熟过程中的表达模式及其mRNA的原位定位。我们显示脊髓和不同的空间格局在P1和P15之间的Hig-1表达增加。在P1脊髓中,我们观察到腹侧背板11和III和腹板IX区域的优先表达。而在P8中,分布更为广泛,整体表达有所增加。 Hig-1在大脑中也广泛表达。原位杂交实验的结果以及有关EST的特殊功能,使我们提出了反义mRNA的表达。引物特异性RT-PCR证实了这种Hig-1转录本的存在,其结构尚未被鉴定。推定的rHig-1蛋白与人类和鼠类预测的序列之间的高度同源性,以及其在中枢神经系统中的特征性表达,表明可能与出生后成熟过程中的细胞凋亡信号传导有关的特定作用。

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