Kato Chiyuki, Mizutani Tomohiro, Tamaki Hisanori, Kumagai Hidehiko, Kamiya Takehiro, Hirobe Ayumi, Fujisawa Yukiko, Kato Hisaharu, Iwasaki Yukimoto
Department of Bioscience, Fukui Prefectural University, 4-1-1 Kenjyojima, Matsuoka-cho, Yoshida-gun, Fukui 910-1195, Japan.
Plant J. 2004 Apr;38(2):320-31. doi: 10.1111/j.1365-313X.2004.02046.x.
Two genes in the rice genome were identified as those encoding the gamma subunits, gamma1 and gamma2, of heterotrimeric G proteins. Using antibodies against the recombinant proteins for the alpha, beta, gamma1, and gamma2 subunits of the G protein complexes, all of the subunits were proven to be localized in the plasma membrane in rice. Gel filtration of solubilized plasma membrane proteins showed that all of the alpha subunits were present in large protein complexes (about 400 kDa) containing the other subunits, beta, gamma1, and gamma2, and probably also some other proteins, whereas large amounts of the beta and gamma (gamma1 and gamma2) subunits were freed from the large complexes and took a 60-kDa form. A yeast two-hybrid assay and co-immunoprecipitation experiments showed that the beta subunit interacted tightly with the gamma1 and gamma2 subunits, and so the beta and gamma subunits appeared to form dimers in rice cells. Some dimers were associated with the alpha subunit, because few beta, gamma1, and gamma2 subunits were present in the 400-kDa complexes in a rice mutant, d1, which was lacking in the alpha subunit. When a constitutively active form of the alpha subunit was prepared by the exchange of one amino acid residue and introduced into d1, the mutagenized subunit was localized in the plasma membrane of the transformants and took a free, and not the 400-kDa, form.
水稻基因组中的两个基因被鉴定为编码异源三聚体G蛋白的γ亚基γ1和γ2。利用针对G蛋白复合物α、β、γ1和γ2亚基的重组蛋白的抗体,证实所有亚基都定位于水稻的质膜中。对溶解的质膜蛋白进行凝胶过滤分析表明,所有α亚基都存在于包含其他亚基β、γ1和γ2以及可能还有其他一些蛋白质的大蛋白复合物(约400 kDa)中,而大量的β和γ(γ1和γ2)亚基从大复合物中游离出来并呈60 kDa的形式。酵母双杂交试验和免疫共沉淀实验表明,β亚基与γ1和γ2亚基紧密相互作用,因此β和γ亚基在水稻细胞中似乎形成二聚体。一些二聚体与α亚基相关联,因为在缺乏α亚基的水稻突变体d1的400 kDa复合物中,β、γ1和γ2亚基很少。当通过交换一个氨基酸残基制备α亚基的组成型活性形式并将其导入d1中时,诱变后的亚基定位于转化体的质膜中,呈游离形式而非400 kDa形式。