Bogdanov Iu F
Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, 119991 Russia.
Genetika. 2003 Apr;39(4):453-73.
Meiosis arose in the evolution of primitive unicellular organisms as a part of sexual process. One type of meiosis, the so-called classical type, predominates in all kingdoms of eukaryotes. Meiosis is controlled by hundreds of genes, both shared with mitosis and specifically meiotic ones. In a wide range of taxa, which in some cases include kingdoms, meiotic genes and features obey Vavilov's law of homologous variation series. Synaptonemal complexes (SCs) temporarily binding homologous chromosomes at prophase I, ensure precise and equal crossing over and interference. SC proteins have 60-80% homology within the class of mammals but differ from the corresponding proteins in fungi and plants. Thus, nonhomologous SC proteins perform similar functions in different taxa. Some recombination enzymes in fungi and insects have common epitopes. The molecular mechanism of recombination is inherited by eukaryotes from prokaryotes and operates in special compartments: SC recombination nodules. Chiasmata, i.e., physical crossovers of nonsister chromatids, are preserved in bivalents until metaphase I due to local cohesion of sister chromatids in the remaining SC fragments. Owing to chiasmata, homologous chromosomes participate in meiosis I in pairs rather than individually, which, along with unipolarity of kinetochores (only in meiosis 1), ensures segregation of homologous chromosomes. The appearance of SC and chiasmata played a key role in the evolution of unicellular organisms since it promoted the development of a progressive type of meiosis. Some lower eukaryotes retain primitive meiosis types. These primitive modes of meiosis also occur in the sex of some insects that is heterozygous for sex chromosomes. I suggest an explanation for these cases. Mutations at meiotic genes impair meiosis; however, due to the preservation of archaic meiotic genes in the genotype, bypass metabolic pathways arise, which provide partial rescue of the traits damaged by mutations. Individual blocks of genetic program of meiotic regulation have probably evolved independently.
减数分裂在原始单细胞生物的进化过程中作为有性生殖过程的一部分而出现。一种减数分裂类型,即所谓的经典类型,在真核生物的所有界中占主导地位。减数分裂由数百个基因控制,这些基因既有与有丝分裂共有的,也有特定的减数分裂基因。在广泛的分类群中,在某些情况下包括界,减数分裂基因和特征遵循瓦维洛夫同源变异系列定律。联会复合体(SCs)在前期I暂时结合同源染色体,确保精确且均等的交叉互换和干涉。SC蛋白在哺乳动物类群中具有60 - 80%的同源性,但与真菌和植物中的相应蛋白不同。因此,非同源的SC蛋白在不同分类群中执行相似的功能。真菌和昆虫中的一些重组酶具有共同的表位。重组的分子机制由真核生物从原核生物继承而来,并在特殊的区域发挥作用:SC重组结节。交叉,即非姐妹染色单体的物理交叉互换,由于剩余SC片段中姐妹染色单体的局部黏连,在二价体中保留到中期I。由于交叉,同源染色体成对而非单个参与减数分裂I,这与动粒的单极性(仅在减数分裂I中)一起,确保了同源染色体的分离。SC和交叉的出现在单细胞生物的进化中起了关键作用,因为它促进了一种进步型减数分裂的发展。一些低等真核生物保留了原始的减数分裂类型。这些原始的减数分裂模式也出现在一些性染色体杂合的昆虫的性别中。我对这些情况提出一种解释。减数分裂基因的突变会损害减数分裂;然而,由于基因型中古老减数分裂基因的保留,出现了旁路代谢途径,这为因突变而受损的性状提供了部分挽救。减数分裂调控的遗传程序的各个模块可能是独立进化的。