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连接蛋白29(GJE1)在小鼠和大鼠耳蜗中的表达模式。

Expression patterns of connexin 29 (GJE1) in mouse and rat cochlea.

作者信息

Yang Jiann-Jou, Liao Pei-Ju, Su Ching-Chyuan, Li Shuan-Yow

机构信息

Genetics Laboratory and Department of BioMedical Sciences, Chung Shan Medical University, Taichung, Taiwan, ROC.

出版信息

Biochem Biophys Res Commun. 2005 Dec 16;338(2):723-8. doi: 10.1016/j.bbrc.2005.09.193. Epub 2005 Oct 11.

Abstract

Multiple types of connexin (Cxs) products, including Cx26, Cx30, Cx31, and Cx43, are found by immunolabeling in the mature cochlea. The transcript of Cx29, a newly discovered member of Cx gene family, was also discovered in the cochlea by cDNA macroarray hybridization. However, the functional roles of Cx29 in the cochlea remain unclear. To elucidate whether the Cx29 gap junction protein epsilon 1, GJE1, is localized in the adult mouse and rat cochlea, we performed an immunohistochemistry (IHC) and reverse transcription-polymerase chain reaction (RT-PCR) analysis. GJE1 was detected in the cochlea neurons, spiral limbus, spiral ligament, organ of Corti, and stria vascularis using IHC analysis. We also show that Cx29 mRNA is present in spiral limbus, spiral ligament, organ of Corti, stria vascularis, and lateral wall by the method of RT-PCR. Higher levels of Cx29 mRNA were found in spiral ligament and spiral limbus, whereas lower level in lateral wall. Our data first provide a comprehensive and detailed pattern of Cx29 gene expression in the mouse and rat cochlea. Knowledge of spatial distribution of Cx29 also allows the identification of candidate genes for deafness and provides important insight into mechanisms that lead to deafness due to mutations in Cx29 gene.

摘要

通过免疫标记在成熟的耳蜗中发现了多种连接蛋白(Cxs)产物,包括Cx26、Cx30、Cx31和Cx43。通过cDNA宏阵列杂交在耳蜗中还发现了Cx基因家族新发现的成员Cx29的转录本。然而,Cx29在耳蜗中的功能作用仍不清楚。为了阐明连接蛋白29缝隙连接蛋白ε1(GJE1)是否定位于成年小鼠和大鼠的耳蜗中,我们进行了免疫组织化学(IHC)和逆转录-聚合酶链反应(RT-PCR)分析。使用免疫组织化学分析在耳蜗神经元、螺旋缘、螺旋韧带、柯蒂氏器和血管纹中检测到了GJE1。我们还通过RT-PCR方法表明Cx29 mRNA存在于螺旋缘、螺旋韧带、柯蒂氏器、血管纹和侧壁中。在螺旋韧带和螺旋缘中发现Cx29 mRNA水平较高,而在侧壁中水平较低。我们的数据首次提供了小鼠和大鼠耳蜗中Cx29基因表达的全面而详细的模式。了解Cx29的空间分布也有助于鉴定耳聋的候选基因,并为因Cx29基因突变导致耳聋的机制提供重要见解。

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