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同步非整倍体和二倍体哺乳动物细胞中的DNA叉移位率。

DNA fork displacement rates in synchronous aneuploid and diploid mammalian cells.

作者信息

Kapp L N, Painter R B

出版信息

Biochim Biophys Acta. 1979 Apr 26;562(2):222-30. doi: 10.1016/0005-2787(79)90168-0.

Abstract

DNA fork displacement rates were measured in Chinese hamster ovary cells (CHO), human HeLa cells and human diploid fibroblasts. For CHO cells two independent techniques were used: one based on CsCl equilibrium density gradients and the other on 313 nm photolysis of incorporated bromodeoxyuridine (BrdUrd). Both methods indicated that there was no significant variation in fork displacement rates in CHO cells as they progressed through S phase. Asynchronous CHO cultures displayed the same average value (1.0 micron/min) and range of values as found in synchronous cells. In contrast, the rate of DNA fork displacement in HeLa cells, measured by the BrdUrd-313 nm method, increased continuously from 0.8 micron/min in early S to 2.5 micron/min in late S. For human diploid fibroblasts, in early S, the rate was approximately 0.7 micron/min and decreased to a minimum of 0.5 micron/min in mid S. The replication fork displacement rate then increased to a maximum of 0.9 micron/min in late S and declined again before the end of S phase. This pattern of DNA fork displacement rates roughly paralleled the overall thymidine incorporation rate and appears quite different from the patterns found for HeLa and CHO cells.

摘要

在中国仓鼠卵巢细胞(CHO)、人宫颈癌HeLa细胞和人二倍体成纤维细胞中测量了DNA叉移位率。对于CHO细胞,使用了两种独立的技术:一种基于CsCl平衡密度梯度,另一种基于掺入的溴脱氧尿苷(BrdUrd)的313nm光解。两种方法均表明,CHO细胞在整个S期进程中叉移位率没有显著变化。异步CHO培养物显示出与同步细胞相同的平均值(1.0微米/分钟)和值范围。相比之下,通过BrdUrd-313nm方法测量的HeLa细胞中的DNA叉移位率从S期早期的0.8微米/分钟持续增加到S期后期的2.5微米/分钟。对于人二倍体成纤维细胞,在S期早期,速率约为0.7微米/分钟,并在S期中段降至最低0.5微米/分钟。复制叉移位率随后在S期后期增加到最大0.9微米/分钟,并在S期结束前再次下降。这种DNA叉移位率模式大致与总的胸苷掺入率平行,并且似乎与HeLa细胞和CHO细胞中发现的模式有很大不同。

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