Krawczun M S, Jenkins E C, Brown W T, Silverman W P
Department of Cytogenetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island.
Am J Med Genet. 1988 May-Jun;30(1-2):435-42. doi: 10.1002/ajmg.1320300145.
The effect of cell density on expression of the fragile site at (X)(q27.3) in short-term whole-blood cultures from patients with fragile X [fra(X)] or Martin-Bell syndrome was studied. A significant increase in fra(X) frequency was observed in 7 of 8 samples when cell density was decreased. Higher fra(X) frequency was not always noted at below-routine density, but in some cases fra(X) expression was depressed at above-routine density. We conclude that decay of the FUdR effect explains the fact that fra(X) expression is affected by culture density. It is significant that a relationship exists between the two; it suggests that in order to maximize fra(X) expression in cases with low-percentage fra(X) with standard methods, cell density may have to be adjusted. It is possible that in individuals who are normally nonexpressing, such as some obligate female carriers and nonpenetrant males, fra(X) expression may be sensitive to cell density effects.
研究了细胞密度对脆性X [fra(X)] 或马丁-贝尔综合征患者短期全血培养中(X)(q27.3) 处脆性位点表达的影响。当细胞密度降低时,8个样本中的7个观察到fra(X) 频率显著增加。并非总是在低于常规密度时注意到较高的fra(X) 频率,但在某些情况下,fra(X) 表达在高于常规密度时会受到抑制。我们得出结论,氟尿苷 (FUdR) 效应的衰减解释了fra(X) 表达受培养密度影响这一事实。两者之间存在关系具有重要意义;这表明,为了用标准方法在fra(X) 百分比低的病例中使fra(X) 表达最大化,可能必须调整细胞密度。在通常不表达的个体中,例如一些 obligate 女性携带者和非外显男性,fra(X) 表达可能对细胞密度效应敏感。