Konovalov A A, Ibragimova S S, Dorogova N V
Institute of Cytology and Genetics, Russian Academy of Sciences, Novosibirsk, 630090 Russia.
Genetika. 2003 Oct;39(10):1328-37.
An additional alcohol dehydrogenase (ADH) activity zone denoted ADH-P ("pollen") has a slightly lower mobility than the major protein ADH1 (the product of structural locus Adh1). This zone is detected in maturing and mature pollen grains and has not been found in any other tissue. ADH-P is detected by electrophoresis in a neutral medium (at pH 7.0-7.2). In an alkaline medium (pH > 8), protein ADH-P is completely inactivated, whereas protein ADH1 retains its activity. ADH-P is a modified variant of the major protein ADH1. Both alleles of the main structural gene (Adh1-F and Adh1-S) undergo modification. The pollen of an FS heterozygote has two variants of the modified enzyme: ADH-PS and ADH-PF. Analysis of segregation in F2 offsprings and test crosses has confirmed that this character is controlled by the only gene Adh-P with allelic variants Adh-P+ (the presence of the modified ADH protein in the pollen) and Adh-P- (the normal protein). Allele Adh-P+ is transmitted through female gametes at a normal frequency (about 1) and through male gametes at a decreased frequency (0.2-0.6), the mean frequency being about 0.4. The frequency of the transmission of allele Adh-P+ through male gametes depends on the genotype of the female parent and the conditions of pollination. Cytoembryological study of microsporogenesis in the Adh-P+/Adh-P- heterozygotes demonstrated an absence of any disturbances in the formation of microspores and pollen grains. Some differences in the formation of pollen tubes on an artificial medium have been observed. It is assumed that the differences between the Adh-P+ and Adh-P- microgametophytes manifest themselves at the progamic phase of fertilization. The possible mechanisms of the formation of the modified ADH-P protein are discussed in connection with the differential activity of genes in the microgametophytes of angiosperms.
另一个酒精脱氢酶(ADH)活性区标记为ADH-P(“花粉”),其迁移率略低于主要蛋白质ADH1(结构基因Adh1的产物)。该区域在成熟和成熟的花粉粒中被检测到,在任何其他组织中均未发现。ADH-P通过在中性介质(pH 7.0 - 7.2)中进行电泳检测。在碱性介质(pH > 8)中,蛋白质ADH-P完全失活,而蛋白质ADH1保留其活性。ADH-P是主要蛋白质ADH1的修饰变体。主要结构基因(Adh1-F和Adh1-S)的两个等位基因都发生修饰。FS杂合子的花粉有两种修饰酶变体:ADH-PS和ADH-PF。对F2后代和测交的分离分析证实,该性状由唯一的基因Adh-P控制,其等位基因变体为Adh-P+(花粉中存在修饰的ADH蛋白)和Adh-P-(正常蛋白)。等位基因Adh-P+通过雌配子以正常频率(约1)传递,通过雄配子以降低的频率(0.2 - 0.6)传递,平均频率约为0.4。等位基因Adh-P+通过雄配子的传递频率取决于母本的基因型和授粉条件。对Adh-P+/Adh-P-杂合子小孢子发生的细胞胚胎学研究表明,小孢子和花粉粒的形成没有任何干扰。在人工培养基上观察到花粉管形成存在一些差异。据推测,Adh-P+和Adh-P-小配子体之间的差异在受精的配子前阶段表现出来。结合被子植物小配子体中基因的差异活性,讨论了修饰的ADH-P蛋白形成的可能机制。