Harger H, Holm D G
Genetics. 1980 Oct;96(2):455-70. doi: 10.1093/genetics/96.2.455.
In females of Drosophila melanogaster, compound autosomes enter the repulsion phase of meiosis uncommitted to a particular segregation pattern because their centromeres are not restricted to a bivalent pairing complex as a consequence of crossing over. Their distribution at anaphase, therefore, is determined by some meiotic property other than exchange pairing, a property that for many years has been associated with the concept of nonhomologous pairing. In the absence of heterologous rearrangements or a free Y chromosome, C(3L) and C(3R) are usually recovered in separate gametes, that is as products of meiotic segregation. Nevertheless, there is a regular, albeit infrequent, recovery of reciprocal meiotic products (the nonsegregational products) that are disomic and nullosomic for compound thirds. The frequency of these exceptions, which is normally between 0.5 and 5.0%, differs for the various strains examined, but remains constant for any given strain. Since previous studies have not uncovered a cause for this base level of nonsegregation, it has been referred to as the spontaneous frequency. In this study, crosses between males and females whose X chromosomes, as well as compound autosomes, are differentially marked reveal a highly significant positive correlation between the frequency of compound-autosome nonsegregation and the frequency of X-chromosome nondisjunction. However, an inverse correlation is found when the frequency of nondisjunction is related to the frequency of crossing over in the proximal region of the X-chromosome. These findings have been examined with reference to the distributive pairing and the chromocentral models and interpreted as demonstrating (1) that nonsegregational meiotic events arise primarily as a result of nonhomologous interactions, (2) that forces responsible for the segregation of nonhomologous chromosomes are properties of the chromocentral region, and (3) that these forces come into expression after the exchange processes are complete.
在黑腹果蝇的雌性个体中,复合常染色体进入减数分裂的排斥期时,并不确定会采取特定的分离模式,因为由于交叉互换,它们的着丝粒并不局限于二价配对复合体。因此,它们在后期的分布是由交换配对以外的某种减数分裂特性决定的,多年来这种特性一直与非同源配对的概念相关联。在没有异源重排或游离Y染色体的情况下,C(3L)和C(3R)通常在单独的配子中被回收,即作为减数分裂分离的产物。然而,对于复合三体,存在规律的(尽管不常见)相互减数分裂产物(非分离产物)的回收,这些产物是二体和缺体。这些例外情况的频率通常在0.5%到5.0%之间,不同检测菌株有所不同,但对于任何给定菌株而言保持恒定。由于先前的研究尚未发现这种基本非分离水平的原因,所以它被称为自发频率。在本研究中,X染色体以及复合常染色体都有不同标记的雄性和雌性之间的杂交显示,复合常染色体非分离频率与X染色体不分离频率之间存在高度显著的正相关。然而,当不分离频率与X染色体近端区域的交叉互换频率相关时,发现呈负相关。这些发现已根据分布配对和染色中心模型进行了研究,并被解释为表明:(1)非分离减数分裂事件主要是由于非同源相互作用产生的;(2)负责非同源染色体分离的力量是染色中心区域的特性;(3)这些力量在交换过程完成后开始表现出来。