Golubovskaya I, Grebennikova Z K, Avalkina N A, Sheridan W F
N.I. Vavilov Institute of Plant Industry, Saint-Petersburg, Russia.
Genetics. 1993 Dec;135(4):1151-66. doi: 10.1093/genetics/135.4.1151.
Understanding the initiation of meiosis and the relationship of this event with other key cytogenetic processes are major goals in studying the genetic control of meiosis in higher plants. Our genetic and structural analysis of two mutant alleles of the ameiotic1 gene (am1 and am1-praI) suggest that this locus plays an essential role in the initiation of meiosis in maize. The product of the ameiotic1 gene affects an earlier stage in the meiotic sequence than any other known gene in maize and is important for the irreversible commitment of cells to meiosis and for crucial events marking the passage from premeiotic interphase into prophase I including chromosome synapsis. It appears that the period of ameiotic1 gene function in meiosis at a minimum covers the interval from some point during premeiotic interphase until the early zygotene stage of meiosis. To study the interaction of genes in the progression of meiosis, several double meiotic mutants were constructed. In these double mutants (i) the ameiotic1 mutant allele was brought together with the meiotic mutation (afd1) responsible for the fixation of centromeres in meiosis; and with the mutant alleles of the three meiotic genes that control homologous chromosome segregation (dv1, ms43 and ms28), which impair microtubule organizing center organization, the orientation of the spindle fiber apparatus, and the depolymerization of spindle filaments after the first meiotic division, respectively; (ii) the afd1 mutation was combined with two mutations (dsy1 and as1) affecting homologous pairing; (iii) the ms43 mutation was combined with the as1, the ms28 and the dv1 mutations; and (iv) the ms28 mutation was combined with the dv1 mutation and the ms4 (polymitotic1) mutations. An analysis of gene interaction in the double mutants led us to conclude that the ameiotic1 gene is epistatic over the afd1, the dv1, the ms43 and the ms28 genes but the significance of this relationship requires further analysis. The afd gene appears to function from premeiotic interphase throughout the first meiotic division, but it is likely that its function begins after the start of the ameiotic1 gene expression. The afd1 gene is epistatic over the two synaptic mutations dsy1 and as1 and also over the dv1 mutation. The new ameiotic*-485 and leptotene arrest*-487 mutations isolated from an active Robertson's Mutator stocks take part in the control of the initiation of meiosis.
了解减数分裂的起始以及该事件与其他关键细胞遗传学过程的关系是研究高等植物减数分裂遗传控制的主要目标。我们对减数分裂1基因(am1和am1-praI)的两个突变等位基因进行的遗传和结构分析表明,该基因座在玉米减数分裂的起始过程中起着至关重要的作用。减数分裂1基因的产物在减数分裂序列中影响的阶段比玉米中任何其他已知基因都要早,对于细胞不可逆地进入减数分裂以及标志着从减数分裂前间期进入前期I的关键事件(包括染色体联会)都很重要。减数分裂1基因在减数分裂中的功能期至少涵盖从减数分裂前间期的某个时间点到减数分裂偶线期早期的时间段。为了研究减数分裂过程中基因的相互作用,构建了几个双减数分裂突变体。在这些双突变体中:(i)减数分裂1突变等位基因与负责减数分裂中着丝粒固定的减数分裂突变(afd1)以及控制同源染色体分离的三个减数分裂基因(dv1、ms43和ms28)的突变等位基因组合在一起,这三个基因分别损害微管组织中心的组织、纺锤体纤维装置的定向以及第一次减数分裂后纺锤体丝的解聚;(ii)afd1突变与影响同源配对的两个突变(dsy1和as1)组合;(iii)ms43突变与as1、ms28和dv1突变组合;(iv)ms28突变与dv1突变和ms4(多有丝分裂1)突变组合。对双突变体中基因相互作用的分析使我们得出结论,减数分裂1基因对afd1、dv1、ms43和ms28基因具有上位性,但这种关系的意义需要进一步分析。afd基因似乎从减数分裂前间期到整个第一次减数分裂都发挥作用,但它的功能可能在减数分裂1基因表达开始后才开始。afd1基因对两个突触突变dsy1和as1以及dv1突变具有上位性。从活跃的罗伯逊易变株系中分离出的新的减数分裂异常-485和细线期停滞-487突变参与了减数分裂起始的控制。