Schmid M, Feichtinger W, Jessberger A, Köhler J, Lange R
Hum Genet. 1986 Sep;74(1):67-73. doi: 10.1007/BF00278788.
The rare fragile site at 16q22 was experimentally induced in lymphocyte cultures with various AT-specific, non-intercalating DNA-ligands. The optimum conditions for the induction of fra(16)(q22) were determined. The best expression of fra(16)(q22) was found with the aromatic diamidine berenil which is recommended for further studies on this fragile site. The results indicate that fra(16)(q22) is a region with AT-rich, late replicating DNA. The simultaneous treatment of lymphocytes with berenil and aphidicolin (inhibitor of DNA polymerase alpha) induces both the rare fra(16)(q22) and the common fra(16)(q23) within the same chromosome. A population study on 350 unselected individuals showed that fra(16)(q22) is the most common of all rare autosomal fragile sites in man. The frequency of individuals heterozygous for fra(16)(q22) is 5.1%, no homozygosity for fra(16)(q22) was detected. Statistical analysis indicates that the population is in Hardy-Weinberg equilibrium with respect to the fragile and non-fragile chromosomes 16.
利用各种特异性针对AT、非嵌入性的DNA配体,在淋巴细胞培养物中通过实验诱导出位于16q22的罕见脆性位点。确定了诱导fra(16)(q22)的最佳条件。发现用芳香二脒贝尼尔能使fra(16)(q22)得到最佳表达,推荐用其对该脆性位点作进一步研究。结果表明,fra(16)(q22)是一个富含AT、复制较晚的DNA区域。用贝尼尔和阿非科林(DNA聚合酶α抑制剂)同时处理淋巴细胞,可在同一染色体内诱导出罕见的fra(16)(q22)和常见的fra(16)(q23)。对350名未经挑选的个体进行群体研究表明,fra(16)(q22)是人类所有罕见常染色体脆性位点中最常见的。fra(16)(q22)杂合个体的频率为5.1%,未检测到fra(16)(q22)纯合子。统计分析表明,就脆性和非脆性16号染色体而言,该群体处于哈迪-温伯格平衡状态。