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新型印记基因Nap1l5和Peg13及其非印记宿主基因在成年小鼠大脑中的表达模式。

Expression patterns of the novel imprinted genes Nap1l5 and Peg13 and their non-imprinted host genes in the adult mouse brain.

作者信息

Davies William, Smith Rachel J, Kelsey Gavin, Wilkinson Lawrence S

机构信息

Developmental Genetics and Neurobiology Programmes, The Babraham Institute, Babraham, Cambridge CB2 4AT, UK.

出版信息

Gene Expr Patterns. 2004 Oct;4(6):741-7. doi: 10.1016/j.modgep.2004.03.008.

Abstract

Recent work has implicated imprinted gene functioning in neurodevelopment and behaviour and defining the expression patterns of these genes in brain tissue has become a key prerequisite to establishing function. In this work we report on the expression patterns of two novel imprinted loci, Nap1l5 and Peg13, in adult mouse brain using in situ hybridisation methods. Nap1l5 and Peg13 are located, respectively, within the introns of the non-imprinted genes Herc3 and the Tularik1 (T1)/KIAA1882 homologue in two separate microimprinted domains on mouse chromosomes 6 and 15. These 'host' genes are highly expressed in brain and consequently we were interested in assessing their expression patterns in parallel to the imprinted genes. The brain expression of all four genes appeared to be mainly neuronal. The detailed expression profiles of Nap1l5 and Peg13 were generally similar with widespread expression that was relatively high in the septal and hypothalamic regions, the hippocampus and the cerebral cortex. In contrast, there was some degree of dissociation between the imprinted genes and their non-imprinted hosts, in that, whilst there was again widespread expression of Herc3 and the T1/KIAA1882 homologue, these genes were also particularly highly expressed in Purkinje neurons and piriform cortex. We also examined expression of the novel imprinted genes in the adrenal glands. Nap1l5 expression was localised mainly to the adrenal medulla, whilst Peg13 expression was observed more generally throughout the adrenal medulla and the outer cortical layers.

摘要

近期的研究表明,印记基因在神经发育和行为中发挥作用,确定这些基因在脑组织中的表达模式已成为确立其功能的关键前提条件。在本研究中,我们运用原位杂交方法,报告了两个新的印记基因座Nap1l5和Peg13在成年小鼠大脑中的表达模式。Nap1l5和Peg13分别位于小鼠6号和15号染色体上两个独立的微印记区域内非印记基因Herc3和Tularik1(T1)/KIAA1882同源基因的内含子中。这些“宿主”基因在大脑中高度表达,因此我们有兴趣并行评估它们与印记基因的表达模式。所有这四个基因在大脑中的表达似乎主要是神经元性的。Nap1l5和Peg13的详细表达谱总体上相似,在隔区、下丘脑区域、海马体和大脑皮层中广泛表达且相对较高。相比之下,印记基因与其非印记宿主之间存在一定程度的分离,即虽然Herc3和T1/KIAA1882同源基因同样广泛表达,但这些基因在浦肯野神经元和梨状皮层中也特别高表达。我们还检测了新印记基因在肾上腺中的表达。Nap1l5的表达主要定位于肾上腺髓质,而Peg13的表达在整个肾上腺髓质和外层皮质中更为普遍。

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