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异戊烯基腺嘌呤作为甲羟戊酸调节DNA复制的介质。

Isopentenyl adenine as a mediator of mevalonate-regulated DNA replication.

作者信息

Huneeus V Q, Wiley M H, Siperstein M D

出版信息

Trans Assoc Am Physicians. 1980;93:347-56.

PMID:7245580
Abstract

The model in Figure 6 may serve to explain these findings. Our previous studies have shown that mevalonic acid is essential for DNA replication and that this function is independent of its role as a cholesterol precursor. The present study suggests that the isoprene purine, isopentenyl adenine, or a related isoprene, may mediate this essential role of mevalonic acid in DNA replication. The fact that isopentenyl adenine will also reverse the inhibition of DNA synthesis caused by nalidixic acid (a compound that does not influence cholesterol synthesis and acts directly on DNA replication) suggests that isopentenyl adenine and nalidixic acid may act at a common reaction site in the process of DNA replication. Finally, these findings provide a possible mechanism by which the early steps of cholesterol synthesis may influence the rate of cell replication in normal cells. Coupled with our earlier observation that the feedback inhibition of mevalonate is lost in all malignant tumors, the present results also suggest that a derangement in these early steps of mevalonic acid metabolism may figure in the transformation of normal cells into cancer cells.

摘要

图6中的模型或许可以解释这些发现。我们之前的研究表明,甲羟戊酸对于DNA复制至关重要,且该功能独立于其作为胆固醇前体的作用。目前的研究表明,异戊二烯嘌呤、异戊烯基腺嘌呤或一种相关的异戊二烯,可能介导了甲羟戊酸在DNA复制中的这一重要作用。异戊烯基腺嘌呤也能逆转萘啶酸(一种不影响胆固醇合成且直接作用于DNA复制的化合物)对DNA合成的抑制作用,这一事实表明,异戊烯基腺嘌呤和萘啶酸可能在DNA复制过程中的一个共同反应位点起作用。最后,这些发现提供了一种可能的机制,通过该机制胆固醇合成的早期步骤可能会影响正常细胞中的细胞复制速率。再结合我们早期观察到的甲羟戊酸的反馈抑制在所有恶性肿瘤中均消失这一现象,目前的结果还表明,甲羟戊酸代谢这些早期步骤的紊乱可能在正常细胞向癌细胞的转化中起作用。

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