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酿酒酵母中两个组蛋白H3-H4基因座编码的mRNA的结构与细胞周期表达比较。

Comparison of the structure and cell cycle expression of mRNAs encoded by two histone H3-H4 loci in Saccharomyces cerevisiae.

作者信息

Cross S L, Smith M M

机构信息

Department of Microbiology, School of Medicine, University of Virginia, Charlottesville 22908.

出版信息

Mol Cell Biol. 1988 Feb;8(2):945-54. doi: 10.1128/mcb.8.2.945-954.1988.

Abstract

The haploid genome of Saccharomyces cerevisiae contains two nonallelic sets of histone H3 and H4 gene pairs, termed the copy I and copy II loci. The structures of the mRNA transcripts from each of these four genes were examined by nuclease protection and primer extension mapping. For each gene, several species of mRNAs were identified that differed in the lengths of their 5' and 3' untranslated regions. The cell cycle accumulation pattern of the H3 and H4 mRNAs was determined in cells from early-exponential-growth cultures fractionated by centrifugal elutriation. The RNA transcripts from all four genes were regulated with the cell division cycle, and transcripts from the nonallelic gene copies showed tight temporal coordination. Cell cycle regulation did not depend on selection of a particular histone mRNA transcript since the ratio of the multiple species from each gene remained the same across the division cycle. Quantitative measurements showed significant differences in the amounts of mRNA expressed from the two nonallelic gene sets. The mRNAs from the copy II H3 and H4 genes were five to seven times more abundant than the mRNAs from the copy I genes. There was no dosage compensation in the steady-state levels of mRNA when either set of genes was deleted. In particular, there was no increase in the amount of copy I H3 or H4 transcripts in cells in which the high-abundance copy II genes were deleted.

摘要

酿酒酵母的单倍体基因组包含两组非等位的组蛋白H3和H4基因对,分别称为拷贝I和拷贝II位点。通过核酸酶保护和引物延伸图谱分析了这四个基因各自的mRNA转录本结构。对于每个基因,鉴定出了几种mRNA,它们在5'和3'非翻译区的长度上有所不同。在通过离心淘析分离的早期指数生长培养物的细胞中,确定了H3和H4 mRNA的细胞周期积累模式。所有四个基因的RNA转录本都受细胞分裂周期调控,并且非等位基因拷贝的转录本表现出紧密的时间协调。细胞周期调控并不依赖于特定组蛋白mRNA转录本的选择,因为每个基因的多种转录本的比例在整个分裂周期中保持不变。定量测量表明,两个非等位基因组表达的mRNA量存在显著差异。拷贝II的H3和H4基因的mRNA比拷贝I基因的mRNA丰富五到七倍。当任何一组基因被删除时,mRNA的稳态水平都没有剂量补偿。特别是,在高丰度的拷贝II基因被删除的细胞中,拷贝I的H3或H4转录本的量没有增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3431/363227/f1ad3c102c70/molcellb00062-0443-a.jpg

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