Ansari A A, Baig M A, Malling H V
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7352-6. doi: 10.1073/pnas.77.12.7352.
This report describes developments toward a cell specific-locus test for measuring point mutations directly in sperm based upon the use of a monospecific antibody against sperm-specific lactate dehydrogenase-X (LDH-X). The antibody recognizes amino acid differences between mouse and rat LDH-X molecules. In general, mouse sperm do not bind the monospecific antibody against rat LDH-X, but a few exceptional mouse sperm do. Such mouse sperm are believed to contain LDH-X molecules in which an amino acid normally present in mouse LDH-X has been exchanged with one present in rat LDH-X at a place where rat and mouse enzymes are antigenically different. Thus, in the fluorescent antibody technique, mouse sperm carrying normal LDH-X do not stain but the sperm containing mutated enzyme do stain. By using this technique, the spontaneous presumptive mutation frequency in DBA/2 mice was found to be 0.43 X 10(-6); it increased to 7.6 X 10(-6) upon procarbazine treatment of the mice.
本报告描述了基于使用针对精子特异性乳酸脱氢酶-X(LDH-X)的单特异性抗体直接在精子中测量点突变的细胞特异性位点测试的进展。该抗体识别小鼠和大鼠LDH-X分子之间的氨基酸差异。一般来说,小鼠精子不与针对大鼠LDH-X的单特异性抗体结合,但有一些特殊的小鼠精子会结合。据信,此类小鼠精子含有LDH-X分子,其中小鼠LDH-X中正常存在的一种氨基酸在大鼠和小鼠酶具有抗原性差异的位置被大鼠LDH-X中存在的一种氨基酸所取代。因此,在荧光抗体技术中,携带正常LDH-X的小鼠精子不染色,但含有突变酶的精子会染色。通过使用该技术,发现DBA/2小鼠的自发推定突变频率为0.43×10^(-6);在用丙卡巴肼处理小鼠后,该频率增加到7.6×10^(-6)。