Smith M W, Ito M, Miyawaki M, Sato S, Yoshikawa Y, Wada S, Maki H, Nakagawa H, Komamine A
Department of Chemical and Biological Sciences, Japan Women's University, Tokyo, Japan.
Plant Physiol. 1997 Jan;113(1):281-91. doi: 10.1104/pp.113.1.281.
Previously, we cloned a carrot (Daucus carota L.) cDNA encoding a 45-kD protein, 21D7, located in the nuclei of proliferating cells. The 21D7 protein is similar to the partial sequence of a regulatory subunit of the bovine 26S proteasome, p58 (G. DeMartino, C.R. Moomaw, O.P. Zagnitko, R.J. Proske, M. Chu-Ping, S.J. Afendis, J.C. Swaffield, C.A. Slaughter [1994] J Biol Chem 269: 20878-20884) and to the deduced sequence encoded by the Saccharomyces cerevisiae gene SUN2 (M. Kawamura, K. Kominami, J. Takeuchi, A. Toh-e [1996] Mol Gen Genet 251: [146-152]). In our work, the expression of plant 21D7 cDNA rescued the yeast sun2 mutant. Fractionation of carrot and spinach (Spinacia oleracea L.) crude extracts showed that the 21D7 protein sedimented with the active 26S proteasomes. The cessation of cell proliferation in carrot suspensions at the stationary phase caused 26S proteasome dissociation and, correspondingly, the 21D7 protein sedimented together with the free regulatory complexes of the 26s proteasomes. Large-scale purification of carrot 26s proteasomes resulted in co-isolation of the 21D7 protein. Polyacrylamide gel electrophoresis under nondenaturing conditions showed that the 21D7 protein had the same mobility as the 26S proteasome and that proteasome dissociation changed the mobility of the 21D7 protein accordingly. We conclude that the 21D7 protein is a subunit of the plant 26S proteasome and that it probably belongs to the proteasome regulatory complex.
此前,我们克隆了一个胡萝卜(Daucus carota L.)cDNA,其编码一种位于增殖细胞核中的45-kD蛋白21D7。21D7蛋白与牛26S蛋白酶体调节亚基p58的部分序列相似(G. DeMartino,C.R. Moomaw,O.P. Zagnitko,R.J. Proske,M. Chu-Ping,S.J. Afendis,J.C. Swaffield,C.A. Slaughter [1994] J Biol Chem 269: 20878 - 20884),也与酿酒酵母基因SUN2编码的推导序列相似(M. Kawamura,K. Kominami,J. Takeuchi,A. Toh-e [1996] Mol Gen Genet 251: [146 - 152])。在我们的研究中,植物21D7 cDNA的表达拯救了酵母sun2突变体。对胡萝卜和菠菜(Spinacia oleracea L.)粗提物进行分级分离表明,21D7蛋白与活性26S蛋白酶体一起沉淀。胡萝卜悬浮液在稳定期细胞增殖的停止导致26S蛋白酶体解离,相应地,21D7蛋白与26S蛋白酶体的游离调节复合物一起沉淀。对胡萝卜26S蛋白酶体进行大规模纯化导致21D7蛋白共分离。非变性条件下的聚丙烯酰胺凝胶电泳表明,21D7蛋白与26S蛋白酶体具有相同的迁移率,并且蛋白酶体解离相应地改变了21D7蛋白的迁移率。我们得出结论,21D7蛋白是植物26S蛋白酶体的一个亚基,并且它可能属于蛋白酶体调节复合物。