Suppr超能文献

Ikappa B(ε) 的核输入与输出功能的表征

Characterization of the nuclear import and export functions of Ikappa B(epsilon).

作者信息

Lee Sang-Hyun, Hannink Mark

机构信息

Biochemistry Department University of Missouri, Columbia, Missouri 65212, USA.

出版信息

J Biol Chem. 2002 Jun 28;277(26):23358-66. doi: 10.1074/jbc.M111559200. Epub 2002 Apr 22.

Abstract

Control over the nuclear localization of nuclear factor kappaB/Rel proteins is accomplished in large part through association with members of the inhibitor of kappaB (IkappaB) protein family. For example, the well studied IkappaBalpha protein actively shuttles between the nucleus and the cytoplasm and both inhibits nuclear import and mediates nuclear export of NF-kappaB/Rel proteins. In contrast, the IkappaBbeta protein can inhibit nuclear import of NF-kappaB/Rel proteins but does not remove NF-kappaB/Rel proteins from the nucleus. To further understand how the IkappaB proteins control the nuclear-cytoplasmic distribution of NF-kappaB/Rel proteins, we have characterized the nuclear import and nuclear export functions of IkappaBepsilon. Our results indicate that the IkappaBepsilon protein, like the IkappaBalpha protein, actively shuttles between the nucleus and the cytoplasm. Similar to IkappaBalpha, nuclear import of IkappaBepsilon is mediated by its ankyrin repeat domain and is not blocked by the dominant-negative RanQ69L protein. However, the nuclear import function of the IkappaBepsilon ankyrin repeat domain is markedly less efficient than that of IkappaBalpha, with the result that nuclear shuttling of IkappaBepsilon between the nucleus and the cytoplasm is significantly slower than IkappaBalpha. Nuclear export of IkappaBepsilon is mediated by a short leucine-rich nuclear export sequence (NES)-like sequence ((343)VLLPFDDLKI(352)), located between amino acids 343 and 352. This NES-like sequence is required for RanGTP-dependent binding of IkappaBepsilon to CRM1. Nuclear accumulation of IkappaB(epsilon) is increased by either leptomycin B treatment or alanine substitutions within the IkappaBepsilon-derived NES. A functional NES is required for both efficient cytoplasmic retention and post-induction control of c-Rel by IkappaBepsilon, consistent with the notion that IkappaBepsilon-mediated nuclear export contributes to control over the nucleocytoplasmic distribution of NF-kappaB/Rel proteins.

摘要

核因子κB/Rel蛋白的核定位控制在很大程度上是通过与κB抑制蛋白(IkappaB)家族成员的结合来实现的。例如,经过充分研究的IkappaBalpha蛋白在细胞核和细胞质之间活跃穿梭,既能抑制核输入,又能介导NF-κB/Rel蛋白的核输出。相比之下,IkappaBbeta蛋白可以抑制NF-κB/Rel蛋白的核输入,但不能将NF-κB/Rel蛋白从细胞核中清除。为了进一步了解IkappaB蛋白如何控制NF-κB/Rel蛋白的核质分布,我们对IkappaBepsilon的核输入和核输出功能进行了表征。我们的结果表明,IkappaBepsilon蛋白与IkappaBalpha蛋白一样,在细胞核和细胞质之间活跃穿梭。与IkappaBalpha类似,IkappaBepsilon的核输入由其锚蛋白重复结构域介导,且不受显性负性RanQ69L蛋白的阻断。然而,IkappaBepsilon锚蛋白重复结构域的核输入功能明显不如IkappaBalpha高效,结果是IkappaBepsilon在细胞核和细胞质之间的穿梭明显慢于IkappaBalpha。IkappaBepsilon的核输出由位于氨基酸343和352之间的一段短的富含亮氨酸的核输出序列(NES)样序列((343)VLLPFDDLKI(352))介导。该NES样序列是RanGTP依赖的IkappaBepsilon与CRM1结合所必需的。通过莱普霉素B处理或IkappaBepsilon衍生的NES内的丙氨酸替代可增加IkappaB(epsilon)的核积累。功能性NES对于IkappaBepsilon有效保留在细胞质以及对c-Rel的诱导后控制都是必需的,这与IkappaBepsilon介导的核输出有助于控制NF-κB/Rel蛋白的核质分布这一观点一致。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验