Johannisson R, Winking H
Institut für Pathologie, Medizinische Universität zu Lübeck, Germany.
Chromosome Res. 1998 Jun;6(4):285-94. doi: 10.1023/a:1009218807304.
Three male mice with trisomy 19 induced by a Robertsonian translocation system were used for the study of meiotic prophase cells and germ cell differentiation. Present in these males were two Robertsonian chromosomes each with a chromosome 19 arm in common, two acrocentric chromosomes corresponding to the second arms of the two Rbs and one acrocentric chromosome 19. These five chromosomes showed a wide range of meiotic pairing configurations. One particular observation was the formation of a true double synaptonemal complex (SC) with three lateral axes and two central elements, which joined the three chromosomes 19 together. Integration of the acrocentric chromosome 19 in a complex pentavalent configuration was seen in 45% of the pachytene nuclei. The proportion of spermatocytes showing association between a quadrivalent and the acrocentric no. 19 was 26%. In 29% of the nuclei, the acrocentric no. 19 was free, integrated or associated with the XY complex, paired with the X chromosome or associated with a bivalent. Finally, in 57% of pachytene cells, the meiotic multivalents or the free univalent 19 were associated with the proximal part of the X chromosome or integrated in the sex chromatin. Therefore, the question arises with regard to the fate of these spermatocytes. The testicular histology shows an arrest of germ cell development at the spermatocyte stage. Several mechanisms seem to be the cause of germ cell depletion in a sequence of different, impaired developmental processes.
三只通过罗伯逊易位系统诱导产生19号染色体三体的雄性小鼠被用于减数分裂前期细胞和生殖细胞分化的研究。这些雄性小鼠体内存在两条罗伯逊染色体,每条都有一条共同的19号染色体臂,两条与两条罗伯逊染色体的第二条臂相对应的近端着丝粒染色体和一条近端着丝粒19号染色体。这五条染色体呈现出广泛的减数分裂配对构型。一个特别的观察结果是形成了一个具有三条侧轴和两个中央元件的真正双价联会复合体(SC),它将三条19号染色体连接在一起。在45%的粗线期细胞核中可以看到近端着丝粒19号染色体整合在一个复杂的五价构型中。显示四价体与近端着丝粒19号染色体之间存在关联的精母细胞比例为26%。在29%的细胞核中,近端着丝粒19号染色体是游离的、整合的或与XY复合体相关联,与X染色体配对或与一个二价体相关联。最后,在57%的粗线期细胞中,减数分裂多价体或游离的单价体19与X染色体的近端部分相关联或整合在性染色质中。因此,这些精母细胞的命运问题随之而来。睾丸组织学显示生殖细胞发育在精母细胞阶段停滞。在一系列不同的、受损的发育过程中,几种机制似乎是生殖细胞耗竭的原因。