Stone D M, Stephens K E, Doles J
Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164-7040.
Cancer Genet Cytogenet. 1993 Feb;65(2):130-4. doi: 10.1016/0165-4608(93)90221-7.
Peripheral blood lymphocytes from three clinically normal domestic cats were cultured for folate-sensitive and aphidicolin-inducible fragile site expression. Induction of folate-sensitive fragile sites was accomplished by culturing cells with trimethoprim plus caffeine. Chromosomes from all cats expressed both folate-sensitive and aphidicolin-inducible breaks and gaps. There were no significant differences between the two methods of fragile site induction in the percentage of cells expressing chromosome breaks and gaps or the mean number of breaks and gaps per cell. All three cats expressed specific chromosome breaks resembling fragile sites at A1q21-22, A1p22, and B1q32. All three sites were induced by aphidicolin. The sites at A1q21-22 and B1q32 were also induced in folate-deficient medium. This is the first report of the induction of chromosomal fragile sites in a feline species.
对三只临床健康的家猫的外周血淋巴细胞进行培养,以检测叶酸敏感型和阿非迪霉素诱导型脆性位点的表达。通过用甲氧苄啶加咖啡因培养细胞来诱导叶酸敏感型脆性位点。所有猫的染色体均表达叶酸敏感型和阿非迪霉素诱导型的断裂和间隙。在表达染色体断裂和间隙的细胞百分比或每个细胞的断裂和间隙平均数方面,两种脆性位点诱导方法之间没有显著差异。所有三只猫均在A1q21 - 22、A1p22和B1q32处表达出类似脆性位点的特定染色体断裂。所有这三个位点均由阿非迪霉素诱导。A1q21 - 22和B1q32处的位点在叶酸缺乏培养基中也被诱导。这是关于在猫科动物中诱导染色体脆性位点的首次报道。