Preiss J, Danner S, Summers P S, Morell M, Barton C R, Yang L, Nieder M
Department of Biochemistry, Michigan State University, East Lansing, Michigan 48824.
Plant Physiol. 1990 Apr;92(4):881-5. doi: 10.1104/pp.92.4.881.
Activity of the enzyme ADPglucose pyrophosphorylase is known to be reduced in maize (Zea mays L.) endosperm mutants at two independent loci, Shrunken-2 (Sh(2)) and Brittle-2 (Bt(2)). Spinach leaf ADPglucose pyrophosphorylase has previously been shown to comprise two subunits of 51 and 54 kilodaltons. Anti-bodies raised to each of the two subunits of spinach leaf ADPglucose pyrophosphorylase were found to cross-react to different bands on Western blots prepared from polyacrylamide gel electrophoresis separated wild-type maize endosperm proteins. The anti-spinach leaf 51 kilodalton subunit antibody cross-reacted with a 55 kilodalton maize endosperm protein and the anti-spinach leaf 54 kilodalton subunit antibody cross-reacted with a 60 kilodalton maize endosperm protein. These immunological reactions were observed in maize endosperm extracts and with a highly purified preparation of maize endosperm ADPglucose pyrophosphorylase. Mutant bt(2) endosperm lacked the 55 kilodalton subunit while mutant sh(2) endosperm lacked the 60 kilodalton subunit on Western blots. These results suggest that the maize endosperm ADPglucose pyrophosphorylase is made up of two immunologically dissimilar subunits and that the bt(2) and sh(2) mutations cause reduction in ADPglucose pyrophosphorylase activity through the lack of one of these two subunits. An ADPglucose pyrophosphorylase cDNA clone antigenically selected from a rice seed cDNA expression library was found to hybridize strongly with a cDNA corresponding to a maize endosperm transcript which is absent in a W64A bt(2) mutant. Thus, the bt(2) mutant causes the absence not only of the small subunit but of the corresponding transcript. Bt(2) is implicated as the structural gene for the small (54 kilodalton) subunit of maize endosperm ADPglucose pyrophosphorylase.
已知在玉米(Zea mays L.)胚乳突变体的两个独立位点,即皱缩-2(Sh(2))和脆-2(Bt(2))处,ADP葡萄糖焦磷酸化酶的活性会降低。菠菜叶ADP葡萄糖焦磷酸化酶先前已被证明由两个分别为51千道尔顿和54千道尔顿的亚基组成。针对菠菜叶ADP葡萄糖焦磷酸化酶两个亚基各自产生的抗体,在由聚丙烯酰胺凝胶电泳分离的野生型玉米胚乳蛋白制备的Western印迹上,被发现与不同条带发生交叉反应。抗菠菜叶51千道尔顿亚基抗体与一个55千道尔顿的玉米胚乳蛋白发生交叉反应,而抗菠菜叶54千道尔顿亚基抗体与一个60千道尔顿的玉米胚乳蛋白发生交叉反应。这些免疫反应在玉米胚乳提取物以及高度纯化的玉米胚乳ADP葡萄糖焦磷酸化酶制剂中均被观察到。在Western印迹上,突变体bt(2)胚乳缺乏55千道尔顿亚基,而突变体sh(2)胚乳缺乏60千道尔顿亚基。这些结果表明,玉米胚乳ADP葡萄糖焦磷酸化酶由两个免疫上不同的亚基组成,并且bt(2)和sh(2)突变通过缺少这两个亚基中的一个导致ADP葡萄糖焦磷酸化酶活性降低。从水稻种子cDNA表达文库中通过抗原筛选得到的一个ADP葡萄糖焦磷酸化酶cDNA克隆,被发现与一个对应于玉米胚乳转录本的cDNA强烈杂交,而该转录本在W64A bt(2)突变体中不存在。因此,bt(2)突变不仅导致小亚基缺失,还导致相应转录本缺失。Bt(2)被认为是玉米胚乳ADP葡萄糖焦磷酸化酶小(54千道尔顿)亚基的结构基因。