Nokkala S, Kuznetsova V G, Maryanska-Nadachowska A, Nokkala C
Laboratory of Genetics, Department of Biology, University of Turku, FIN-20014, Turku, Finland.
Chromosome Res. 2006;14(5):559-65. doi: 10.1007/s10577-006-1053-6. Epub 2006 Jul 12.
The modes of orientation and segregation of the sex chromosome trivalent X1X2Y in male meiosis of Cacopsylla mali (Psylloidea, Homoptera) were analysed. Males with an X1X2Y sex chromosome system coexist with males displaying a neo-XY system in populations of this species. The fusion chromosome resulting in the formation of a trivalent in meiosis originates from the fusion of an autosome with the neo-Y chromosome. In the majority of metaphase I cells (92.4%) the X1X2Y trivalent showed co-orientation; X1 and X2 chromosomes oriented towards one pole whereas the Y oriented towards the opposite pole. In the rest of the cells (7.6%) the trivalent with subterminal chiasmata was oriented parallel to the equatorial plane. From this orientation the trivalent produced triple chromatids joined together by undivided telomeric parts of chromosomes and hence by sister chromatid cohesion at anaphase I. In the majority of metaphase II cells the orientation of triple chromatids suggested the production of unbalanced gametes. However, in a small number of cells (1.7%) the trivalent showed co-orientation of X1X2 with Y. Both the first division and second division co-orientations, or 94.1% of divisions as a whole, were estimated to yield balanced gametes, containing either X1 and X2 chromosomes or Y chromosome. It was concluded that, since the triple chromatid contained undivided telomere regions at metaphase II, which divided at anaphase II, the orientation of the trivalent with its longitudinal axis parallel to the equatorial plane in metaphase I also represents co-orientation and results in pre-reduction. The existence of post-reductional behaviour of holocentric bivalents and multivalents is discussed.
分析了苹果木虱(木虱科,同翅目)雄性减数分裂中性染色体三体X1X2Y的定向和分离模式。在该物种的种群中,具有X1X2Y性染色体系统的雄性与显示新XY系统的雄性共存。减数分裂中导致形成三体的融合染色体起源于一条常染色体与新Y染色体的融合。在大多数中期I细胞(92.4%)中,X1X2Y三体显示共定向;X1和X2染色体朝向一极,而Y朝向相反极。在其余细胞(7.6%)中,具有亚末端交叉的三体与赤道平面平行定向。从这种定向来看,三体产生由染色体未分开的端粒部分连接在一起的三联染色单体,因此在后期I通过姐妹染色单体凝聚连接在一起。在大多数中期II细胞中,三联染色单体的定向表明产生不平衡配子。然而,在少数细胞(1.7%)中,三体显示X1X2与Y共定向。据估计,第一次分裂和第二次分裂的共定向,或总体上94.1%的分裂,产生平衡配子,包含X1和X2染色体或Y染色体。得出的结论是,由于三联染色单体在中期II包含未分开的端粒区域,在后期II分开,所以在中期I三体的纵轴与赤道平面平行的定向也代表共定向并导致前期减数。还讨论了全着丝粒二价体和多价体的后期减数行为的存在。