Lopes M A, Coleman C E, Kodrzycki R, Lending C R, Larkins B A
Department of Plant Sciences, University of Arizona, Tucson 85721.
Mol Gen Genet. 1994 Dec 1;245(5):537-47. doi: 10.1007/BF00282216.
The soft, starchy endosperm of the maize (Zea mays L.) floury 2 mutant is associated with a reduction in zein mRNA and protein synthesis, unique protein body morphology, and enhanced levels of a 70 kDa protein, that has been shown to be the maize homolog of a chaperonin found in the endoplasmic reticulum. We found an unusual alpha-zein protein of 24 kDa to be consistently associated with the zein fraction from floury 2 mutants. Three additional alpha-zein proteins with molecular weights ranging from ca. 25 to 27 kDa are detected in the storage protein fraction of a high percentage of floury 2 kernels and a low percentage of normal kernels in a genetically segregating population. The four proteins in a genetically segregating population. The four proteins can be distinguished from one another by immunostaining on Western blots. Synthesis of the 24 kDa protein is regulated by Opaque2, since the 24 kDa protein is lacking in the storage protein fraction of opaque2/floury2 double mutants. The synthesis of an abnormal alpha-zein protein in floury2 could explain many features of the mutant, such as the abnormal protein body morphology, induction of the 70 kDa chaperonin, and hypostasis to opaque2 (o2). Although we cannot prove that the accumulation of this protein is responsible for the floury2 phenotype, we were able to detect a restriction fragment length polymorphism (RFLP) linked to the floury2 locus with a 22 kDa alpha-zein probe. We hypothesize that the unique characteristics of the floury2 mutant could be a response to the accumulation of a defective alpha-zein protein which impairs secretory protein synthesis.
玉米(Zea mays L.)粉质2突变体的柔软、富含淀粉的胚乳与醇溶蛋白mRNA和蛋白质合成减少、独特的蛋白体形态以及一种70 kDa蛋白质水平升高有关,该蛋白质已被证明是内质网中发现的伴侣蛋白的玉米同源物。我们发现一种异常的24 kDaα-醇溶蛋白始终与粉质2突变体的醇溶蛋白组分相关。在一个遗传分离群体中,高比例的粉质2籽粒和低比例的正常籽粒的贮藏蛋白组分中检测到另外三种分子量约为25至27 kDa的α-醇溶蛋白。这四种蛋白质在遗传分离群体中。这四种蛋白质可以通过蛋白质免疫印迹法进行免疫染色来相互区分。24 kDa蛋白质的合成受不透明2调控,因为在不透明2/粉质2双突变体的贮藏蛋白组分中缺乏24 kDa蛋白质。粉质2中异常α-醇溶蛋白的合成可以解释该突变体的许多特征,如异常的蛋白体形态、70 kDa伴侣蛋白的诱导以及对不透明2(o2)的下位性。虽然我们不能证明这种蛋白质的积累是粉质2表型的原因,但我们能够用一个22 kDaα-醇溶蛋白探针检测到一个与粉质2基因座连锁的限制性片段长度多态性(RFLP)。我们推测,粉质2突变体的独特特征可能是对一种有缺陷的α-醇溶蛋白积累的反应,这种蛋白会损害分泌蛋白的合成。