Wang G H
Yi Chuan Xue Bao. 1989;16(1):67-73.
To further illustrate the biological significance of variant NOR (including double NOR--dNOR and triple NOR--tNOR) and satellite association (SA) and the relationship to meiotic non-disjunction (NDJ), this study was carried out in the normal population and the parents of patients with Down Syndrome (DS). Of 800 individuals, 4 dNOR carriers, two of them from the control and two from the non-informative experiments were detected. SA data for 3 out of the 4 dNOR carriers showed no statistical significant increase in SA when dNOR was present in the cell even in case 4 where two dNOR were found in one cell. However, ease 3 demonstrated significant decrease in SA when dNOR was present, although it showed that the overall incidence of dNOR was higher in this carrier than that in the other three. It is concluded that dNOR can be detected on any acrocentric chromosome and not be related to NDJ of chromosome, which is a heritable variant that does not affect phenotype and that there are two kinds of dNOR variants, one being from the translocation of the short arm of acrocentric chromosome, the other from non-translocation.
为了进一步阐明变异核仁组织区(包括双份核仁组织区——dNOR和三份核仁组织区——tNOR)及随体联合(SA)的生物学意义以及它们与减数分裂不分离(NDJ)的关系,本研究在正常人群及唐氏综合征(DS)患者的父母中开展。在800名个体中,检测到4名dNOR携带者,其中两名来自对照组,两名来自无信息实验。4名dNOR携带者中有3名的SA数据显示,即使在一个细胞中发现两个dNOR的病例4中,当细胞中存在dNOR时,SA也没有统计学上的显著增加。然而,病例3显示当存在dNOR时SA显著降低,尽管该携带者中dNOR的总体发生率高于其他三人。得出的结论是,dNOR可在任何近端着丝粒染色体上检测到,且与染色体的NDJ无关,它是一种不影响表型的可遗传变异,并且存在两种dNOR变异体,一种来自近端着丝粒染色体短臂的易位,另一种来自非易位。