Basu A., Basu U., Taylor G. J.
Department of Botany, University of Alberta, Edmonton, Alberta T6G 2E9, Canada.
Plant Physiol. 1994 Mar;104(3):1007-1013. doi: 10.1104/pp.104.3.1007.
Three-day-old seedlings of an Al-sensitive (Neepawa) and an Al-resistant (PT741) cultivar of Triticum aestivum were subjected to Al concentrations ranging from 0 to 100 [mu]M for 72 h. At 25 [mu]M Al, growth of roots was inhibited by 57% in the Al-sensitive cultivar, whereas root growth in the Al-resistant cultivar was unaffected. A concentration of 100 [mu]M Al was required to inhibit root growth of the Al-resistant cultivar by 50% and resulted in almost total inhibition of root growth in the sensitive cultivar. Cytoplasmic and microsomal membrane fractions were isolated from root tips (first 5 mm) and the adjacent 2-cm region of roots of both cultivars. When root cytoplasmic proteins were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, no changes in polypeptide patterns were observed in response to Al stress. Analysis of microsomal membrane proteins revealed a band with an apparent molecular mass of 51 kD, which showed significant accumulation in the resistant cultivar following Al exposure. Two-dimensional gel analysis revealed that this band comprises two polypeptides, each of which is induced by exposure to Al. The response of the 51-kD band to a variety of experimental conditions was characterized to determine whether its pattern of accumulation was consistent with a possible role in Al resistance. Accumulation was significantly greater in root tips when compared to the rest of the root. When seedlings were subjected to Al concentrations ranging from 0 to 150 [mu]M, the proteins were evident at 25 [mu]M and were fully accumulated at 100 [mu]M. Time-course studies from 0 to 96 h indicated that full accumulation of the 51-kD band occurred within 24 h of initiation of Al stress. With subsequent removal of stress, the polypeptides gradually disappeared and were no longer visible after 72 h. When protein synthesis was inhibited by cycloheximide, the 51-kD band disappeared even when seedlings were maintained in Al-containing media. Other metals, including Cu, Zn, and Mn, failed to induce this band, and Cd and Ni resulted in its partial accumulation. These results indicate that synthesis of the 51-kD microsomal membrane proteins is specifically induced and maintained during Al stress in the Al-resistant cultivar, PT741.
对普通小麦的一个铝敏感品种(Neepawa)和一个铝抗性品种(PT741)的3日龄幼苗施加浓度范围为0至100μM的铝,处理72小时。在25μM铝浓度下,铝敏感品种的根生长受到57%的抑制,而铝抗性品种的根生长未受影响。需要100μM的铝浓度才能使铝抗性品种的根生长受到50%的抑制,并导致敏感品种的根生长几乎完全受到抑制。从两个品种的根尖(最初5毫米)和相邻的2厘米根区域分离出细胞质和微粒体膜组分。当通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析根细胞质蛋白时,未观察到多肽模式因铝胁迫而发生变化。微粒体膜蛋白分析显示出一条表观分子量为51kD的条带,在铝处理后的抗性品种中该条带显著积累。二维凝胶分析表明,这条带由两条多肽组成,每条多肽都是由铝处理诱导产生的。对51kD条带在各种实验条件下的反应进行了表征,以确定其积累模式是否与在铝抗性中可能发挥的作用一致。与根的其余部分相比,根尖中的积累明显更多。当幼苗受到浓度范围为0至150μM的铝处理时,这些蛋白在25μM时可见,并在100μM时完全积累。从0至96小时的时间进程研究表明,51kD条带在铝胁迫开始后24小时内完全积累。随着随后胁迫的解除,这些多肽逐渐消失,72小时后不再可见。当用环己酰亚胺抑制蛋白质合成时,即使幼苗保持在含铝培养基中,51kD条带也会消失。其他金属,包括铜、锌和锰,未能诱导出这条带,而镉和镍导致其部分积累。这些结果表明,在铝抗性品种PT741中,51kD微粒体膜蛋白的合成在铝胁迫期间被特异性诱导并维持。