Lemke Johannes, Claussen Jan, Michel Susanne, Chudoba Ilse, Mühlig Peter, Westermann Martin, Sperling Karl, Rubtsov Nikolai, Grummt Ulrich-Walter, Ullmann Peter, Kromeyer-Hauschild Katrin, Liehr Thomas, Claussen Uwe
Institute of Human Genetics and Anthropology, Friedrich Schiller University, Jena, Germany.
Am J Hum Genet. 2002 Nov;71(5):1051-9. doi: 10.1086/344286. Epub 2002 Oct 7.
In contrast to those of metaphase chromosomes, the shape, length, and architecture of human interphase chromosomes are not well understood. This is mainly due to technical problems in the visualization of interphase chromosomes in total and of their substructures. We analyzed the structure of chromosomes in interphase nuclei through use of high-resolution multicolor banding (MCB), which paints the total shape of chromosomes and creates a DNA-mediated, chromosome-region-specific, pseudocolored banding pattern at high resolution. A microdissection-derived human chromosome 5-specific MCB probe mixture was hybridized to human lymphocyte interphase nuclei harvested for routine chromosome analysis, as well as to interphase nuclei from HeLa cells arrested at different phases of the cell cycle. The length of the axis of interphase chromosome 5 was determined, and the shape and MCB pattern were compared with those of metaphase chromosomes. We show that, in lymphocytes, the length of the axis of interphase chromosome 5 is comparable to that of a metaphase chromosome at 600-band resolution. Consequently, the concept of chromosome condensation during mitosis has to be reassessed. In addition, chromosome 5 in interphase is not as straight as metaphase chromosomes, being bent and/or folded. The shape and banding pattern of interphase chromosome 5 of lymphocytes and HeLa cells are similar to those of the corresponding metaphase chromosomes at all stages of the cell cycle. The MCB pattern also allows the detection and characterization of chromosome aberrations. This may be of fundamental importance in establishing chromosome analyses in nondividing cells.
与中期染色体相比,人类间期染色体的形状、长度和结构尚未得到很好的理解。这主要是由于在整体观察间期染色体及其亚结构时存在技术问题。我们通过使用高分辨率多色带(MCB)分析了间期细胞核中染色体的结构,MCB能够描绘染色体的整体形状,并以高分辨率创建一种由DNA介导的、染色体区域特异性的假彩色带型模式。将微切割获得的人类5号染色体特异性MCB探针混合物与用于常规染色体分析的人类淋巴细胞间期细胞核杂交,以及与处于细胞周期不同阶段的HeLa细胞间期细胞核杂交。确定了间期5号染色体轴的长度,并将其形状和MCB模式与中期染色体的进行了比较。我们发现,在淋巴细胞中,间期5号染色体轴的长度与600条带分辨率下的中期染色体长度相当。因此,有必要重新评估有丝分裂期间染色体浓缩的概念。此外,间期的5号染色体不像中期染色体那样笔直,而是弯曲和/或折叠的。淋巴细胞和HeLa细胞间期5号染色体的形状和带型模式在细胞周期的所有阶段都与相应的中期染色体相似。MCB模式还允许检测和表征染色体畸变。这对于在非分裂细胞中建立染色体分析可能具有至关重要的意义。