The translocon SEC61 localized in the inner nuclear membrane transports membrane-embedded EGF receptor to the nucleus.

ASIA unversity > 醫學暨健康學院 > 生物科技學系 > 期刊論文 > Item 310904400/16173

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://asiair.asia.edu.tw/ir/handle/310904400/16173

题名:	The translocon SEC61 localized in the inner nuclear membrane transports membrane-embedded EGF receptor to the nucleus.
作者:	洪明奇;Hung, Mien-Chie
贡献者:	生物科技學系
关键词:	Breast Cancer;Intracellular Trafficking;Nuclear Transport;Oncogene;Receptor Tyrosine Kinase
日期:	2010
上传时间:	2012-11-23 09:09:30 (UTC+0)
摘要:	Accumulating evidence indicates that endocytosis plays an essential role in the nuclear transport of the ErbB family members, such as epidermal growth factor receptor (EGFR) and ErbB-2. Nevertheless, how full-length receptors embedded in the endosomal membrane pass through the nuclear pore complexes and function as non-membrane-bound receptors in the nucleus remains unclear. Here we show that upon EGF treatment, the biotinylated cell surface EGFR is trafficked to the inner nuclear membrane (INM) through the nuclear pore complexes, remaining in a membrane-bound environment. We further find that importin β regulates EGFR nuclear transport to the INM in addition to the nucleus/nucleoplasm. Unexpectedly, the well known endoplasmic reticulum associated translocon Sec61β is found to reside in the INM and associate with EGFR. Knocking down Sec61β expression reduces EGFR level in the nucleoplasm portion and accumulates it in the INM portion. Thus, the Sec61β translocon plays an unrecognized role in the release of the membrane-anchored EGFR from the lipid bilayer of the INM to the nucleus. The newly identified Sec61β function provides an alternative pathway for nuclear transport that can be utilized by membrane-embedded proteins such as full-length EGFR.
關聯:	JOURNAL OF BIOLOGICAL CHEMISTRY
显示于类别:	[生物科技學系] 期刊論文

文件中的档案:

档案	描述	大小	格式	浏览次数
index.html		0Kb	HTML	349	检视/开启

在ASIAIR中所有的数据项都受到原著作权保护.

数据加载中.....