Pro-apoptotic ASY/Nogo-B protein associates with ASYIP

被引:35
作者
Qi, B
Qi, YP
Watari, A
Yoshioka, N
Inoue, H
Mimemoto, Y
Yamashita, K
Sasagawa, T
Yutsudo, M
机构
[1] Wuhan Univ, Inst Virol, Wuhan, Hubei, Peoples R China
[2] Osaka Univ, Microbial Dis Res Inst, Yamadaoka, Japan
[3] Shiga Univ Med Sci, Otsu, Shiga 52021, Japan
[4] Fac Pharmaceut Sci, Kanazawa, Ishikawa, Japan
[5] Kanazawa Univ, Sch Med, Kanazawa, Ishikawa 920, Japan
关键词
D O I
10.1002/jcp.10297
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously shown that ectopic expression of the ASY/Nogo-B gene induced apoptosis in various cancer cell lines. Nogo-A, a splice variant of the ASY, has been reported to have an inhibitory effect on neuronal regeneration in the central nervous system. To investigate the mechanism of ASY-induced apoptosis or inhibition of neuronal regeneration, we cloned a cDNA for the ASY-interacting protein from the human cDNA library using the yeast two-hybrid method, and obtained a cDNA we designated as ASYIP. The ASYIP protein contains two hydrophobic regions and a double lysine endoplasmic reticulum (ER) retrieval motif at its C-terminus, which was shown to be identical to RTN3, a reticulon family protein of unknown function. We showed that ASY and ASYIP proteins formed a complex also in human cells. Mutational analysis indicated that both of the hydrophobic regions of the ASYIP protein were required for the association. By immunofluorescence analysis, the ASYIP protein was shown to be co-localized with ASY in the ER. Characterization of the ASYIP gene may be very useful in clarifying the mechanism of ASY-induced apoptosis or Nogo-involved inhibition of neuronal regeneration in the central nervous system. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:312 / 318
页数:7
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