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在酵母S期全程都需要Cdc7来激活复制起点。

Cdc7 is required throughout the yeast S phase to activate replication origins.

作者信息

Donaldson A D, Fangman W L, Brewer B J

机构信息

Department of Genetics, University of Washington, Seattle, Washington 98195-7360, USA.

出版信息

Genes Dev. 1998 Feb 15;12(4):491-501. doi: 10.1101/gad.12.4.491.

Abstract

The long-standing conclusion that the Cdc7 kinase of Saccharomyces cerevisiae is required only to trigger S phase has been challenged by recent data that suggests it acts directly on individual replication origins. We tested the possibility that early- and late-activated origins have different requirements for Cdc7 activity. Cells carrying a cdc7(ts) allele were first arrested in G1 at the cdc7 block by incubation at 37 degrees C, and then were allowed to enter S phase by brief incubation at 23 degrees C. During the S phase, after return to 37 degrees C, early-firing replication origins were activated, but late origins failed to fire. Similarly, a plasmid with a late-activated origin was defective in replication. As a consequence of the origin activation defect, duplication of chromosomal sequences that are normally replicated from late origins was greatly delayed. Early-replicating regions of the genome duplicated at approximately their normal time. The requirements of early and late origins for Cdc7 appear to be temporally rather than quantitatively different, as reducing overall levels of Cdc7 by growth at semi-permissive temperature reduced activation at early and late origins approximately equally. Our results show that Cdc7 activates early and late origins separately, with late origins requiring the activity later in S phase to permit replication initiation.

摘要

长期以来的结论是,酿酒酵母的Cdc7激酶仅在触发S期时才是必需的,但最近的数据对这一结论提出了挑战,这些数据表明它直接作用于单个复制起点。我们测试了早期和晚期激活的起点对Cdc7活性有不同要求的可能性。携带cdc7(ts)等位基因的细胞首先在37℃孵育,使其在cdc7阻滞点停滞在G1期,然后通过在23℃短暂孵育使其进入S期。在S期,回到37℃后,早期启动的复制起点被激活,但晚期起点未能启动。同样,带有晚期激活起点的质粒在复制方面存在缺陷。由于起点激活缺陷,通常从晚期起点复制的染色体序列的复制被大大延迟。基因组的早期复制区域在大约正常时间进行复制。早期和晚期起点对Cdc7的要求似乎在时间上而非数量上有所不同,因为在半许可温度下生长以降低Cdc7的总体水平,会大致同等程度地降低早期和晚期起点的激活。我们的结果表明,Cdc7分别激活早期和晚期起点,晚期起点需要在S期后期有活性才能启动复制。

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