Hahn P J
Department of Radiology, State University of New York Health Science Center, Syracuse.
Bioessays. 1993 Jul;15(7):477-84. doi: 10.1002/bies.950150707.
Double-minute chromosomes play a critical role in tumor cell genetics where they are frequently associated with the overexpression of oncogene products. They have been observed for many years in light microscopic examinations of metaphase chromosomes from tumor cells, but their origin remains unknown and is the subject of considerable speculation. However, molecular details of their structure and organization can now be described in conjunction with the microscopic examinations, to allow an evaluation of the various models that have been developed to explain the genesis of double-minutes. The evidence now favors simple models that invoke chromosome breakage and circularization of very large acentric chromosome fragments, permitting unequal segregation of the genes on the fragment during cell division. If there is selection for overexpression of one of the genes on the fragment, daughter cells with more fragments will grow faster than daughter cells with fewer fragments, and over time the population of cells will come to contain many double-minutes per cell.
双微体染色体在肿瘤细胞遗传学中起着关键作用,它们常与癌基因产物的过表达相关。多年来,在对肿瘤细胞中期染色体进行光学显微镜检查时都能观察到它们,但其起源仍然未知,并且是大量推测的主题。然而,现在可以结合显微镜检查来描述它们结构和组织的分子细节,以便评估为解释双微体的起源而提出的各种模型。目前的证据支持简单模型,该模型认为染色体断裂以及非常大的无着丝粒染色体片段的环化,使得片段上的基因在细胞分裂过程中发生不等分离。如果片段上的某个基因的过表达受到选择,含有更多片段的子细胞将比含有较少片段的子细胞生长得更快,随着时间的推移,细胞群体中将每个细胞都含有许多双微体。