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FRA16D的晚期/缓慢复制在常见脆性位点诱导中的作用。

The role of late/slow replication of the FRA16D in common fragile site induction.

作者信息

Palakodeti Aparna, Han Yu, Jiang Yanwen, Le Beau Michelle M

机构信息

Section of Hematology/Oncology, and the Cancer Research Center, The University of Chicago, Chicago, Illinois 60637, USA.

出版信息

Genes Chromosomes Cancer. 2004 Jan;39(1):71-6. doi: 10.1002/gcc.10290.

Abstract

The FRA16D, at 16q23, spans the WWOX gene and is one of the most highly expressed common fragile sites observed when DNA replication is perturbed by aphidicolin. Several lines of evidence suggest that fragile sites are regions of DNA that are unusually sensitive to interference during replication. We have determined that the FRA16D alleles replicate in a synchronous fashion and that replication of these sequences occurs primarily in late S phase extending into G2 phase. Exposure to aphidicolin, an inhibitor of DNA polymerase alpha, results in a modest increase in cells with replication of FRA16D sequences in early S phase. This may represent initiation of replication in early S phase coupled with slow replication progression, or, alternatively, these cells may have passed through mitosis, entered the G1-S phase of the next cell cycle, and initiated replication/repair. Our results support a model in which common fragile sites are sequences that may initiate replication in early-mid S phase but are slow to complete replication, and the chromosomal breaks and gaps observed in metaphase cells result from unreplicated DNA.

摘要

位于16q23的FRA16D跨越WWOX基因,是当DNA复制受到阿非科林干扰时观察到的表达水平最高的常见脆性位点之一。多条证据表明,脆性位点是DNA中在复制过程中对干扰异常敏感的区域。我们已经确定FRA16D等位基因以同步方式复制,并且这些序列的复制主要发生在S期后期并延伸至G2期。暴露于DNA聚合酶α抑制剂阿非科林会导致在S期早期具有FRA16D序列复制的细胞适度增加。这可能代表S期早期复制的起始以及缓慢的复制进程,或者,这些细胞可能已经经历有丝分裂,进入下一个细胞周期的G1-S期,并启动复制/修复。我们的结果支持一种模型,即常见脆性位点是可能在S期早期至中期起始复制但复制完成缓慢的序列,并且在中期细胞中观察到的染色体断裂和间隙是由未复制的DNA导致的。

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