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裂殖酵母细胞周期突变体中的组蛋白转录。

Histone transcription in cell cycle mutants of fission yeast.

机构信息

Department of Biophysics, Faculty of Science, Kyoto University, Kyoto, Japan.

出版信息

EMBO J. 1987 Apr;6(4):1093-7. doi: 10.1002/j.1460-2075.1987.tb04863.x.

Abstract

The level of histone H2B transcripts peak during S-phase of the fission yeast Schizosaccharomyces pombe. The pattern of transcript accumulation has been monitored in temperature-sensitive mutants which block at different times during the cell cycle, at start in G1 where the cell becomes committed to the mitotic cycle, in G1 after start, and during S-phase. Cells blocked before start using cdc10-129 do not accumulate histone H2B transcripts, but cells blocked after start using cdc22-C11 do show accumulation. Transcript levels increase in another mutant cdc20-M10 which also blocks in G1. These experiments establish that histone H2B transcripts increase in level in preparation for S-phase during late G1 before any DNA synthesis. Passage of start begins a sequence of events leading to S-phase which includes an increase in histone H2B transcript levels. In the cdc20 and cdc22 mutants transcript levels do not decrease normally suggesting that the signals which lead to the fall in level are not given in these G1-arrested cells. The mutants cdc17-K42 (defective in DNA ligase) and cdc24-M38 block in late S-phase after the DNA content has doubled. Histone H2B transcripts increase normally but remain at a high level. In these mutants even though DNA content has doubled, the mechanisms which lead to a fall in transcript levels appear not to be brought into play.

摘要

裂殖酵母 Schizosaccharomyces pombe 的组蛋白 H2B 转录本水平在 S 期达到峰值。在不同细胞周期时间点阻断的温度敏感突变体中,已经监测到转录本积累的模式,这些突变体在 G1 期开始时阻断,此时细胞开始进入有丝分裂周期,在 G1 期开始后阻断,以及在 S 期阻断。使用 cdc10-129 阻断在开始之前的细胞不会积累组蛋白 H2B 转录本,但使用 cdc22-C11 阻断在开始之后的细胞会显示出积累。另一个突变体 cdc20-M10 也在 G1 期阻断,其转录本水平增加。这些实验表明,在任何 DNA 合成之前的晚期 G1 期,组蛋白 H2B 转录本水平增加,为 S 期做准备。起始的通过开始了一系列导致 S 期的事件,其中包括组蛋白 H2B 转录本水平的增加。在 cdc20 和 cdc22 突变体中,转录本水平不会正常下降,这表明在这些 G1 期阻滞的细胞中,没有给出导致水平下降的信号。突变体 cdc17-K42(DNA 连接酶缺陷)和 cdc24-M38 在 DNA 含量翻倍后的晚期 S 期阻断。组蛋白 H2B 转录本正常增加,但仍保持高水平。在这些突变体中,即使 DNA 含量翻倍,导致转录本水平下降的机制似乎也没有被激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f195/553507/b0ba53c8cb42/emboj00244-0253-a.jpg

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