Zatsepina O V, Noniashvili E M, Chentsov Iu S, Dyban A P
Tsitologiia. 1987 Jan;29(1):12-6.
The structural organization of the mouse metaphase chromosomes in the early embryonic development (I-IV cleavages) was studied using serial ultrathin section. It was shown that in the first cleavage the metaphase chromosomes consist of DNP fibrils 20-25 nm in diameter, which are distributed nonuniformly along the chromosomes. It was suggested that parts of chromosomal arms formed by tightly packing DNP fibrils may correspond to the G-bands revealed by the routine Giemsa staining. In metaphase chromosomes of 8-16-cell embryos DNP fibrils form chromonema--thick threads about 90 nm in diameter. The chromonemata are evenly organized along chromosomal arms. The centromeric heterochromatin always consists of DNP fibrils tightly arranged in a block having no chromonemal level of organization. In all the cells studied chromosomes form structural contacts (associations) by their centromeric heterochromatin regions.
利用连续超薄切片技术研究了小鼠早期胚胎发育(Ⅰ-Ⅳ次卵裂)中期染色体的结构组织。结果表明,在第一次卵裂时,中期染色体由直径为20-25nm的脱氧核蛋白(DNP)纤维组成,这些纤维沿染色体分布不均匀。有人提出,由紧密堆积的DNP纤维形成的染色体臂部分可能对应于常规吉姆萨染色显示的G带。在8-16细胞胚胎的中期染色体中,DNP纤维形成染色线——直径约90nm的粗线。染色线沿染色体臂均匀排列。着丝粒异染色质始终由紧密排列成块状的DNP纤维组成,没有染色线水平的组织。在所有研究的细胞中,染色体通过其着丝粒异染色质区域形成结构接触(关联)。