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Intracellular targeting and homotetramer formation of a truncated inositol 1,4,5-trisphosphate receptor-green fluorescent protein chimera in Xenopus laevis oocytes: Evidence for the involvement of the transmembrane spanning domain in endoplasmic reticulum targeting and homotetramer complex formation
被引:51
|作者:
Sayers, LG
Miyawaki, A
Muto, A
Takeshita, H
Yamamoto, A
Michikawa, T
Furuichi, T
Mikoshiba, K
机构:
[1] TSUKUBA LIFE SCI CTR,INST PHYS & CHEM RES,MOL NEUROBIOL LAB,IBARAKI,OSAKA 305,JAPAN
[2] ERATO,EXPLORATORY RES ADV TECHNOL,CALCIOSIGNAL NET PROJECT,TOKYO 153,JAPAN
[3] KANSAI MED UNIV,DEPT PHYSIOL,MORIGUCHI,OSAKA 570,JAPAN
关键词:
D O I:
10.1042/bj3230273
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In an attempt to define structural regions of the type I inositol 1,4,5-trisphosphate [Ins(1,4,5)P-3] receptor [Ins(1,4,5)P(3)R] involved in its intracellular targeting to the endoplasmic reticulum (ER), we have employed the use of green fluorescent protein (GFP) to monitor the localization of a truncated Ins(1,4,5)P(3)R mutant containing just the putative transmembrane spanning domain and the C-terminal cytoplasmic domain [amino acids 2216-2749; termed inositol trisphosphate receptor(ES)]. We expressed a chimeric GFP-Ins(1,4,5)P(3)R(ES) fusion protein in Xenopus laevis oocytes, and used fluorescence confocal microscopy to monitor its intracellular localization. Fluorescence confocal microscopy data showed an intense fluorescence in the perinuclear region and in a reticular-network under the animal pole of the oocyte, consistent with the targeting of expressed GFP-Ins(1,4,5)P(3)R(ES) to perinuclear ER and ER under the animal pole. These findings are consistent with the intracellular localization of the endogenous Xenopus Ins(1,4,5)P(3)R shown previously. Furthermore, electron microscopy data indicate that expressed GFP-Ins(1,4,5)P(3)R(ES) is in fact targeted to the ER. Sodium carbonate extraction of microsomal membranes and cross-linking experiments indicate that the expressed chimeric protein is in fact membrane anchored and able to form a homotetrameric complex. Our data provides evidence that Ins(1,4,5)P(3)R(ES) constitutes the membrane spanning domain of the Ins(1,4,5)P(3)R and is able to mediate homotetramer formation, without the need for the large N-terminal cytoplasmic domain. Furthermore, the localization of GFP-Ins(1,4,5)P(3)R(ES) on the ER indicates that an ER retention/targeting signal is contained within the transmembrane spanning domain of the inositol trisphosphate receptor.
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页码:273 / 280
页数:8
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