Grell R F
Basic Life Sci. 1985;36:317-35. doi: 10.1007/978-1-4613-2127-9_22.
Normal females developing at 25 degrees C produce their first population of oocytes at 132 +/- 2 hr post oviposition. Entrance of the oocytes into premeiotic interphase signals initiation of DNA replication which continues for 30 hr. Coincidentally, extensive SCs appear, averaging 50 microns (132 hr), peaking at 75 microns (144 hr), and continuing into early vitellarial stages. Recombinational response to heat, evidenced by enhancement or induction of exchange, is limited to the S-phase with a peak at 144 hr coinciding with maximal extension of the SC. Coincidence of synapsis and recombination response with S at premeiotic interphase is contrary to their conventional localization at meiotic prophase. The interrelationship between exchange and nondisjunction has been clarified by the Distributive Pairing Model of meiosis. Originally revealed through high frequencies of nonrandom assortment of nonhomologous chromosomes, distributive pairing has been shown to follow and to be noncompetitive with exchange, to be based on size-recognition, not homology, and as a raison d'etre, to provide a segregational mechanism for noncrossover homologs. Rearrangements, recombination mutants, and aneuploids may contribute noncrossover chromosomes to the distributive pool and so promote the nonhomologous associations responsible for nondisjunction of homologs and regular segregation of nonhomologs. Further information concerning early meiotic events and their relation to segregation has been revealed by studies of the ts rec-1(26) mutant. Application of the restrictive temperature (31 degrees C) at sequential times during development shows wild-type activity to be drastically reduced beginning at 126/132 hr, terminating at 162 hr, and so coinciding with S and the heat-sensitive period of the normal genome. EMs of serially sectioned oocyte nuclei maintained at the restrictive or control temperature reveal SCs to be indistinguishable, and implicate recombination rather than synapsis as the target of the mutant. Activity of rec-1(26) in the range 17 degrees to 31 degrees C reveals a sharp decline between 28+ degrees and 31 degrees C, typical of a denaturation curve. If denaturation of the rec protein by the restrictive temperature marks its active phase, it follows that recombination terminates at the end of S when the restrictive temperature becomes ineffective. The notion that synapsis ensures regular segregation (35) is invalidated by rec-1(26) whose normal synapsis at the restrictive temperature is followed by a 200-fold increase in nondisjunction at segregation, as compared to the control.(ABSTRACT TRUNCATED AT 400 WORDS)
在25摄氏度下发育的正常雌性在产卵后132±2小时产生第一批卵母细胞。卵母细胞进入减数分裂前间期标志着DNA复制的开始,DNA复制持续30小时。与此同时,大量的联会复合体出现,平均长度为50微米(132小时),在75微米时达到峰值(144小时),并持续到早期卵黄形成阶段。对热的重组反应,通过交换的增强或诱导来证明,仅限于S期,在144小时达到峰值,与联会复合体的最大延伸相吻合。减数分裂前间期联会和重组反应与S期的巧合与它们在减数分裂前期的传统定位相反。交换与不分离之间的相互关系已通过减数分裂的分配配对模型得到阐明。最初通过非同源染色体的非随机分配的高频率揭示,分配配对已被证明跟随交换且与交换无竞争关系,基于大小识别而非同源性,并且作为存在的理由,为非交叉同源染色体提供一种分离机制。重排、重组突变体和非整倍体可能将非交叉染色体贡献给分配池,从而促进负责同源染色体不分离和非同源染色体正常分离的非同源关联。对ts rec-1(26)突变体的研究揭示了关于早期减数分裂事件及其与分离关系的更多信息。在发育过程中的连续时间施加限制温度(31摄氏度)表明,野生型活性从126/132小时开始急剧下降,在162小时终止,因此与S期和正常基因组的热敏感时期相吻合。对维持在限制温度或对照温度下的卵母细胞核进行连续切片的电子显微镜观察表明,联会复合体无法区分,并暗示重组而非联会是突变体的靶点。rec-1(26)在17摄氏度至31摄氏度范围内的活性显示在28摄氏度以上和31摄氏度之间急剧下降,这是变性曲线的典型特征。如果限制温度导致rec蛋白变性标志着其活性阶段,那么可以推断重组在S期末期终止,此时限制温度变得无效。联会确保正常分离的观点(35)被rec-1(26)推翻,与对照相比,rec-1(26)在限制温度下正常联会,随后在分离时不分离增加200倍。(摘要截断于400字)