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天然延伸转录本测序揭示了裂殖酵母中正义和反义新生转录之间的整体反相关。

Native elongating transcript sequencing reveals global anti-correlation between sense and antisense nascent transcription in fission yeast.

机构信息

ncRNA, epigenetic and genome fluidity, Institut Curie, PSL Research University, CNRS UMR 3244, Université Pierre et Marie Curie, 75248 Paris Cedex 05, France.

URPHYM, Namur Research College (NARC), University of Namur, Namur 5000, Belgium.

出版信息

RNA. 2018 Feb;24(2):196-208. doi: 10.1261/rna.063446.117. Epub 2017 Nov 7.

Abstract

Antisense transcription can regulate sense gene expression. However, previous annotations of antisense transcription units have been based on detection of mature antisense long noncoding (aslnc)RNAs by RNA-seq and/or microarrays, only giving a partial view of the antisense transcription landscape and incomplete molecular bases for antisense-mediated regulation. Here, we used native elongating transcript sequencing to map genome-wide nascent antisense transcription in fission yeast. Strikingly, antisense transcription was detected for most protein-coding genes, correlating with low sense transcription, especially when overlapping the mRNA start site. RNA profiling revealed that the resulting aslncRNAs mainly correspond to cryptic Xrn1/Exo2-sensitive transcripts (XUTs). ChIP-seq analyses showed that antisense (as)XUT's expression is associated with specific histone modification patterns. Finally, we showed that asXUTs are controlled by the histone chaperone Spt6 and respond to meiosis induction, in both cases anti-correlating with levels of the paired-sense mRNAs, supporting physiological significance to antisense-mediated gene attenuation. Our work highlights that antisense transcription is much more extended than anticipated and might constitute an additional nonpromoter determinant of gene regulation complexity.

摘要

反义转录可以调节有义基因的表达。然而,之前对反义转录单元的注释是基于 RNA-seq 和/或微阵列检测成熟的反义长非编码(aslnc)RNAs,这仅提供了反义转录景观的部分视图和反义介导调节的不完整分子基础。在这里,我们使用天然延伸转录测序在裂殖酵母中绘制全基因组新生反义转录图谱。引人注目的是,大多数编码蛋白的基因都检测到了反义转录,这与低有义转录相关,尤其是当重叠 mRNA 起始位点时。RNA 分析显示,产生的 aslncRNAs 主要对应于隐藏的 Xrn1/Exo2 敏感转录本(XUTs)。ChIP-seq 分析表明,反义(as)XUT 的表达与特定的组蛋白修饰模式相关。最后,我们表明 asXUTs 受组蛋白伴侣 Spt6 的控制,并对减数分裂诱导有反应,在这两种情况下,与配对有义 mRNAs 的水平呈反相关,支持反义介导的基因衰减具有生理意义。我们的工作强调了反义转录比预期的更为广泛,可能构成了基因调控复杂性的另一个非启动子决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/318a/5769747/645cd4094072/196f01.jpg

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