Abbott A G, Hess J E, Gerbi S A
Chromosoma. 1981;83(1):1-18. doi: 10.1007/BF00286012.
Meiosis I of spermatogenesis in the fungus fly, Sciara coprophila, has a monopolar spindle which collects the maternal and supernumerary L chromosome sets, while the paternal chromosomes migrate away from the single pole to be excluded in a bud. By inspection, the metacentric paternal chromosome IV moves with its centromere lagging rather than leading the direction of motion. Therefore, we wondered if all paternal homologues move in such a reverse orientation. To determine the orientation of the other homologues which are acrocentrics (chromosomes II, III, X), their centromeres were localized by use of the DAPI C-bonding technique. In addition, we characterized centromeric heterochromatin on polytene chromosomes by C-banding and in situ hybridization of satellite DNA isolated by Ag+-Cs2SO4 (rho CsC1 satellite I=1.698 g/ml; rho CsC1 satellite II=1.705 g/ml). The two satellite fractions were localized to the centromeric heterochromatin of all the chromosomes, and to a varying degree to all chromosome telomeres. By DAPI C-banding we could precisely locate each centromere band on polytene chromosomes, and these results agreed with those of satellite cRNA in situ hybridization. We then applied the DAPI C-banding technique to primary spermatocyte preparations, and determined that all paternal chromosomes migrate at anaphase I with their centromeres lagging rather than leading movement to the cell periphery. Since in polytene chromosomes the X chromosome contains a moderately fluorescent band on its noncentromeric end as well, in order to clarify its DAPI C-banding result in primary spermatocytes, we did in situ hybridization of (3)H nick-translated cloned rDNA, since rDNA is a convenient marker for the centromeric heterochromatin of the X. These data and the DAPI C-banding results indicate that the X as well as all th other paternal homologues display a reverse orientation (centromeres lag) as they migrate away from the single spindle pole to the cell periphery. - One model explaining this unusual paternal chromosome orientation is that there may be unique neocentromeric-like attachments to the non-centromeric free ends of these chromosomes. These attachments could serve to pull the paternal chromosomes to the cellular periphery as anaphase I progresses. In order to test this model, we analyzed anaphase I spermatocytes after a terminal block of heterochromatin had been removed from metacentric paternal chromosome IV by X-irradiation. We observed that when metacentric paternal chromosome IV is broken, it maintains its inverted "V" orientation rather than assuming a rod-like configuration. These data imply that there are no unique, terminal neocentromeric attachments to paternal chromosome IV as it progresses to the cellular periphery.
在粪蝇(Sciara coprophila)精子发生的减数分裂I过程中,会形成一个单极纺锤体,它收集母本和额外的L染色体组,而父本染色体则从单极移开,被排除在一个芽体中。经观察,具中央着丝粒的父本染色体IV移动时,其着丝粒滞后,而非引领运动方向。因此,我们想知道所有父本同源染色体是否都以这种反向方式移动。为了确定其他具近端着丝粒的同源染色体(染色体II、III、X)的移动方向,我们利用DAPI C带技术定位了它们的着丝粒。此外,我们通过C带以及对用Ag⁺ - Cs₂SO₄分离的卫星DNA进行原位杂交,对多线染色体上的着丝粒异染色质进行了表征(rho CsC1卫星I = 1.698 g/ml;rho CsC1卫星II = 1.705 g/ml)。这两个卫星组分定位于所有染色体的着丝粒异染色质,并且在不同程度上也定位于所有染色体的端粒。通过DAPI C带,我们能够在多线染色体上精确地定位每个着丝粒带,这些结果与卫星cRNA原位杂交的结果一致。然后我们将DAPI C带技术应用于初级精母细胞标本,确定所有父本染色体在减数分裂后期I移动时,其着丝粒滞后,而非引领向细胞周边的移动。由于在多线染色体中,X染色体在其非着丝粒末端也有一条中等荧光带,为了阐明其在初级精母细胞中的DAPI C带结果,我们对³H缺口平移克隆的rDNA进行了原位杂交,因为rDNA是X染色体着丝粒异染色质的一个方便标记。这些数据和DAPI C带结果表明,X染色体以及所有其他父本同源染色体在从单极纺锤体极向细胞周边移动时,都呈现反向(着丝粒滞后)。 - 一个解释这种异常父本染色体方向的模型是,这些染色体的非着丝粒自由末端可能存在独特的类新着丝粒附着。随着减数分裂后期I的进行,这些附着可能会将父本染色体拉向细胞周边。为了验证这个模型,我们分析了经X射线照射后,具中央着丝粒的父本染色体IV上的异染色质终末阻断被去除后的减数分裂后期I精母细胞。我们观察到,当具中央着丝粒的父本染色体IV断裂时,它保持其倒“V”形方向,而不是呈现棒状形态。这些数据表明,在具中央着丝粒的父本染色体IV向细胞周边移动的过程中,不存在独特的末端类新着丝粒附着。