Feon S A, Valerius R M, Genetet N M, Bernard-Griffiths I, Le Prise P Y, Le Gall E J, David J C
Laboratoire de Biochimie du Développement UA CNRS Université de Rennes, France.
Blood. 1988 Aug;72(2):648-54.
DNA ligase activity was determined in the WBCs from 306 cases of acute lymphoblastic leukemia (ALL) and acute nonlymphocytic leukemia (ANLL). In T-ALL cells this activity was either low or absent. DNA analysis by nucleoid, alkaline elution, and alkaline sucrose centrifugation after cells were embedded in agarose inserts has shown more DNA breaks in T-ALL than in ANLL blasts. Phytohemagglutinin stimulation of T-ALL blasts resulted in the apparent joining of the DNA breaks. Apparent identical results can be obtained by the incubation of DNA with exogenous DNA ligase. The authors suggest that this enzyme is a crucially regulated step of replication and subsequent proliferation in this type of leukemia.
对306例急性淋巴细胞白血病(ALL)和急性非淋巴细胞白血病(ANLL)患者的白细胞进行了DNA连接酶活性检测。在T-ALL细胞中,这种活性要么很低,要么不存在。将细胞包埋在琼脂糖插块中后,通过核小体、碱性洗脱和碱性蔗糖密度离心进行DNA分析,结果显示T-ALL中的DNA断裂比ANLL原始细胞更多。用植物血凝素刺激T-ALL原始细胞会导致DNA断裂明显连接。将DNA与外源性DNA连接酶一起孵育可得到明显相同的结果。作者认为,这种酶是这类白血病复制及后续增殖的一个关键调控步骤。