Tease C
Mammalian Genetics Unit, Medical Research Council, Harwell, Didcot, Oxfordshire OX11 0RD, UK.
Chromosoma. 1998 Dec;107(8):549-58. doi: 10.1007/s004120050341.
Two factors postulated to influence the meiotic behaviour of reciprocal translocations were investigated. Firstly, variation in the length of translocated and non-translocated segments was studied in male mice using four different rearrangements involving chromosomes 2 and 4. Secondly, sex-related effects were analysed through comparison of the meiotic behaviour of two translocations in male and female germ cells. In the first part of the study, primary and secondary spermatocytes of male mice carrying a translocation [T(2;4)1Ca, T(2;4)13H, T(2;4)1Sn, or T(2;4)1Go] were screened. Each rearrangement had different proportions of cells with ring and chain quadrivalents at metaphase I; the T(2;4)1Sn heterozygote also had a high rate (45%) of translocation bivalents. In general, the translocations had elevated chiasma frequencies in the rearranged chromosomes compared with structurally normal chromosomes 2 and 4, although the extent of the effect varied. Each rearrangement produced a different array of segregation products at metaphase II, reflecting their contrasting frequencies of multivalent configurations at metaphase I. Comparison of chromosome behaviour at metaphase I and II suggested that certain configurations tended to adopt particular orientations. However, it was also clear that such correlations were imprecise and that other factors, possibly the exact positions of chiasmata, also played a role in multivalent orientation. Two rearrangements, T(2;4)1Go and T(7;16)67H, were analysed in female mice. The frequencies of the various multivalent types at metaphase I differed from those in male carriers of these rearrangements owing to an increased chiasma frequency in oocytes in some of the pairing segments. Not surprisingly, the segregation products seen in metaphase II cells showed some differences from the pattern recorded in male germ cells. For T(2;4)1Go, the sex-related difference in segregation patterns resulted in a diminished expectation of genetically imbalanced gametes, although this was not the case for T(7;16)67H.
研究了假定影响相互易位减数分裂行为的两个因素。首先,在雄性小鼠中利用涉及2号和4号染色体的四种不同重排研究了易位和非易位片段长度的变化。其次,通过比较两种易位在雄性和雌性生殖细胞中的减数分裂行为来分析性别相关效应。在研究的第一部分,对携带易位【T(2;4)1Ca、T(2;4)13H、T(2;4)1Sn或T(2;4)1Go】的雄性小鼠的初级和次级精母细胞进行了筛选。每种重排在中期I具有不同比例的带有环状和链状四价体的细胞;T(2;4)1Sn杂合子也有很高比例(45%)的易位二价体。一般来说,与结构正常的2号和4号染色体相比,易位在重排染色体上具有更高的交叉频率,尽管影响程度有所不同。每种重排在中期II产生了不同的分离产物阵列,反映了它们在中期I多价体构型频率的差异。对中期I和II染色体行为的比较表明,某些构型倾向于采取特定的取向。然而,同样明显的是,这种相关性并不精确,其他因素,可能是交叉的确切位置,也在多价体取向上发挥了作用。在雌性小鼠中分析了两种重排,T(2;4)1Go和T(7;16)67H。由于某些配对片段中卵母细胞交叉频率增加,中期I各种多价体类型的频率与这些重排的雄性携带者不同。不出所料,中期II细胞中看到的分离产物与雄性生殖细胞中记录的模式存在一些差异。对于T(2;4)1Go,分离模式中的性别相关差异导致遗传不平衡配子的预期减少,尽管T(7;16)67H并非如此。