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一种新型Cx43伴侣蛋白CIP150的分子克隆与功能分析

Molecular cloning and functional analysis of a novel Cx43 partner protein CIP150.

作者信息

Akiyama Motofusa, Ishida Norihiro, Ogawa Takuya, Yogo Keiichiro, Takeya Tatsuo

机构信息

Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0129, Japan.

出版信息

Biochem Biophys Res Commun. 2005 Oct 7;335(4):1264-71. doi: 10.1016/j.bbrc.2005.08.019.

Abstract

We identified and cloned a novel gene encoding a partner protein, CIP150, of connexin 43 (Cx43). CIP150 associates with Cx43 through its carboxyl terminal domain. Conversely, a region consisting of 16 amino acids in the juxtamembrane region (amino acids 227-242) in the carboxyl terminal tail of Cx43 was identified to be responsible for the association. A variant of Cx43 lacking this region was expressed only in a nonphosphorylated form and appeared to lose the capacity to localize to the region of cell-cell contact and dye transfer activity. When the expression of CIP150 was suppressed using small interfering RNA, the localization to the plasma membrane as well as dye transfer activity of Cx43 was significantly reduced. These results suggest that the newly identified domain is essential for the proper phosphorylation and localization of Cx43, and CIP150 is a novel partner protein targeting this domain.

摘要

我们鉴定并克隆了一个编码连接蛋白43(Cx43)的伴侣蛋白CIP150的新基因。CIP150通过其羧基末端结构域与Cx43结合。相反,在Cx43羧基末端尾巴的近膜区域(氨基酸227 - 242)中由16个氨基酸组成的区域被确定为负责这种结合。缺乏该区域的Cx43变体仅以非磷酸化形式表达,并且似乎失去了定位于细胞 - 细胞接触区域和染料转移活性的能力。当使用小干扰RNA抑制CIP150的表达时,Cx43向质膜的定位以及染料转移活性显著降低。这些结果表明,新鉴定的结构域对于Cx43的适当磷酸化和定位至关重要,并且CIP15着是靶向该结构域的新型伴侣蛋白。

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