Woloszynska Magdalena, Kanczewska Justyna, Drabkin Artem, Maudoux Olivier, Dambly Stéphanie, Boutry Marc
Unité de Biochimie physiologique, Institut des Sciences de la Vie, Université catholique de Louvain, Croix du Sud, Belgium.
Ann N Y Acad Sci. 2003 Apr;986:198-203. doi: 10.1111/j.1749-6632.2003.tb07160.x.
Plant plasma membrane H(+)-ATPases are encoded by a family of about ten genes organized into five subfamilies. Subfamilies I and II contain the most widely and highly expressed genes. In Nicotiana plumbaginifolia, they are represented, respectively, by pma2 (plasma membrane H(+)-ATPase) and pma4. When expressed in the yeast Saccharomyces cerevisiae, the two isoforms show different kinetics and are differently regulated by phosphorylation of the penultimate threonine residue and binding of regulatory 14-3-3 proteins. To determine if these differences also occurred in plant tissues, we developed an experimental approach allowing the characterization of a single isoform in the plant. When PMA2 bearing a 6-His tag was expressed under a strong transcription promoter in Nicotiana tabacum BY2 cells, solubilized from microsomal membranes and purified, the penultimate threonine was found to be phosphorylated, thus validating the model.
植物质膜H(+) -ATP酶由一个约含十个基因的家族编码,这些基因被组织成五个亚家族。亚家族I和II包含表达最广泛且表达水平最高的基因。在烟草中,它们分别由pma2(质膜H(+) -ATP酶)和pma4代表。当在酿酒酵母中表达时,这两种同工型表现出不同的动力学特性,并且受倒数第二个苏氨酸残基的磷酸化作用以及调节性14-3-3蛋白的结合作用的调控方式也不同。为了确定这些差异是否也出现在植物组织中,我们开发了一种实验方法,可对植物中的单一同工型进行表征。当带有6-组氨酸标签的PMA2在烟草BY2细胞的强转录启动子下表达、从微粒体膜中溶解并纯化后,发现倒数第二个苏氨酸被磷酸化,从而验证了该模型。