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用于DNA合成化学抑制研究的显微注射脱氧核苷酸

Microinjected deoxynucleotides for the study of chemical inhibition of DNA synthesis.

作者信息

Wawra E

机构信息

Institut für Molekularbiologie der Universität Wien, Austria.

出版信息

Nucleic Acids Res. 1988 Jun 24;16(12):5249-61. doi: 10.1093/nar/16.12.5249.

Abstract

Microinjection is shown to be a useful tool for studies of chemical inhibition of DNA synthesis: inhibitor-treated cells were injected with combinations of radioactive precursors and their uptake into DNA was monitored by autoradiography. The results obtained from inhibition by cytosinearabinoside, aphidicolin, trifluorothymidine, and fluorodeoxyuridine agreed well with the common knowledge about these drugs. Short-term (but not long-term) treatments with methotrexate were compensated by injections of thymidine-nucleotides. The effect of hydroxyurea was in part, but not fully, reversed by injection of all four deoxytriphosphates; this implies a second mechanism besides inhibition of ribonucleotide reductase. Regulation of reductase was responsible for the effect of thymidine: the enhanced dTTP caused a depletion of dCTP and dATP. Novobiocin was different from all other drugs tested, DNA polymerase or enzymes of the precursor metabolism are obviously not targets of this drug.

摘要

显微注射被证明是研究DNA合成化学抑制作用的一种有用工具:将放射性前体组合注射到经抑制剂处理的细胞中,并通过放射自显影监测它们被摄取到DNA中的情况。从胞嘧啶阿拉伯糖苷、阿非迪霉素、三氟胸苷和氟脱氧尿苷抑制作用获得的结果与关于这些药物的常识非常吻合。甲氨蝶呤的短期(但非长期)处理可通过注射胸苷核苷酸得到补偿。羟基脲的作用部分(但非完全)可通过注射所有四种脱氧三磷酸核苷来逆转;这意味着除了抑制核糖核苷酸还原酶之外还有第二种机制。还原酶的调节是胸苷产生作用的原因:dTTP的增加导致dCTP和dATP的消耗。新生霉素与所有其他测试药物不同,DNA聚合酶或前体代谢酶显然不是这种药物的作用靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4495/336765/4df058a392ee/nar00155-0035-a.jpg

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