GRIP domain proteins, locating to the trans-Golgi network, are thought to play an essential role in Golgi apparatus trafficking in yeast and animal cells. In the present study, AtGRIP cDNA was amplified by reverse tra...GRIP domain proteins, locating to the trans-Golgi network, are thought to play an essential role in Golgi apparatus trafficking in yeast and animal cells. In the present study, AtGRIP cDNA was amplified by reverse transcriptase PCR from RNA isolated from Arabidopsis seedling. The GST fusion protein of AtGRIP was affinity-purified and its rabbit polyclonal antibody was obtained. Immuno-blotting with the purified anti-AtGRIP polyclonal antibody demonstrated that the molecular mass of AtGRIP protein is about 92 kD, and its expression is not tissue-specific in Arabidopsis. Immunoflourescent labeling and confocal microscopy revealed that the AtGRIP protein was co-localized with Golgi stacks in Arabidopsis root cells. Immuno-gold labeling and electron microscopy observation showed that AtGRIP protein was mainly located to the membrane of the secretory vesicles of trans-Golgi network in Arabidopsis root cap cells. Taken together, these results indicate that the localization of GRIP domain proteins between plants and animal cells are conserved. These results also suggest that the AtGRIP may be involved in regulating the formation or sorting of Golgi-associated vesicles in plant cells.展开更多
本文分析了三套(T、C、S、N)与20对(C、N)玉米同核异质系,在25℃条件下,经 C 毒素(HMC)处理3小时后,观察根冠细胞的死亡率。结果表明,C 细胞质的细胞死亡率均高于其它同核异质系。因此,C 毒素对 C 细胞质的毒害作用是特异性的,同时也为...本文分析了三套(T、C、S、N)与20对(C、N)玉米同核异质系,在25℃条件下,经 C 毒素(HMC)处理3小时后,观察根冠细胞的死亡率。结果表明,C 细胞质的细胞死亡率均高于其它同核异质系。因此,C 毒素对 C 细胞质的毒害作用是特异性的,同时也为快速鉴定玉米雄花不育细胞质提供了一种新方法。展开更多
基金the National Natural Science Foundation of China (Grant Nos. 30570924 and 30721062)
文摘GRIP domain proteins, locating to the trans-Golgi network, are thought to play an essential role in Golgi apparatus trafficking in yeast and animal cells. In the present study, AtGRIP cDNA was amplified by reverse transcriptase PCR from RNA isolated from Arabidopsis seedling. The GST fusion protein of AtGRIP was affinity-purified and its rabbit polyclonal antibody was obtained. Immuno-blotting with the purified anti-AtGRIP polyclonal antibody demonstrated that the molecular mass of AtGRIP protein is about 92 kD, and its expression is not tissue-specific in Arabidopsis. Immunoflourescent labeling and confocal microscopy revealed that the AtGRIP protein was co-localized with Golgi stacks in Arabidopsis root cells. Immuno-gold labeling and electron microscopy observation showed that AtGRIP protein was mainly located to the membrane of the secretory vesicles of trans-Golgi network in Arabidopsis root cap cells. Taken together, these results indicate that the localization of GRIP domain proteins between plants and animal cells are conserved. These results also suggest that the AtGRIP may be involved in regulating the formation or sorting of Golgi-associated vesicles in plant cells.
