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古菌C/D盒小RNA生物合成的可塑性

Plasticity of archaeal C/D box sRNA biogenesis.

作者信息

Tripp Vanessa, Martin Roman, Orell Alvaro, Alkhnbashi Omer S, Backofen Rolf, Randau Lennart

机构信息

Max Planck Institute for Terrestrial Microbiology, Karl-von-Frisch Strasse 10, Marburg, 35043, Germany.

LOEWE Center for Synthetic Microbiology, SYNMIKRO, Karl-von-Frisch-Strasse 16, Marburg, 35043, Germany.

出版信息

Mol Microbiol. 2017 Jan;103(1):151-164. doi: 10.1111/mmi.13549. Epub 2016 Oct 29.

Abstract

Archaeal and eukaryotic organisms contain sets of C/D box s(no)RNAs with guide sequences that determine ribose 2'-O-methylation sites of target RNAs. The composition of these C/D box sRNA sets is highly variable between organisms and results in varying RNA modification patterns which are important for ribosomal RNA folding and stability. Little is known about the genomic organization of C/D box sRNA genes in archaea. Here, we aimed to obtain first insights into the biogenesis of these archaeal C/D box sRNAs and analyzed the genetic context of more than 300 archaeal sRNA genes. We found that the majority of these genes do not possess independent promoters but are rather located at positions that allow for co-transcription with neighboring genes and their start or stop codons were frequently incorporated into the conserved boxC and D motifs. The biogenesis of plasmid-encoded C/D box sRNA variants was analyzed in vivo in Sulfolobus acidocaldarius. It was found that C/D box sRNA maturation occurs independent of their genetic context and relies solely on the presence of intact RNA kink-turn structures. The observed plasticity of C/D box sRNA biogenesis is suggested to enable their accelerated evolution and, consequently, allow for adjustments of the RNA modification landscape.

摘要

古菌和真核生物含有一组C/D盒小(核仁)RNA,其引导序列决定了靶RNA的核糖2'-O-甲基化位点。这些C/D盒小RNA组的组成在不同生物之间高度可变,导致不同的RNA修饰模式,这对核糖体RNA的折叠和稳定性很重要。关于古菌中C/D盒小RNA基因的基因组组织知之甚少。在这里,我们旨在初步了解这些古菌C/D盒小RNA的生物合成,并分析了300多个古菌小RNA基因的遗传背景。我们发现,这些基因中的大多数没有独立的启动子,而是位于允许与相邻基因共转录的位置,并且它们的起始或终止密码子经常被纳入保守的boxC和D基序中。在嗜热栖热菌中对质粒编码的C/D盒小RNA变体的生物合成进行了体内分析。发现C/D盒小RNA的成熟与其遗传背景无关,仅依赖于完整的RNA扭结-转角结构的存在。C/D盒小RNA生物合成中观察到的可塑性被认为能够使其加速进化,从而允许调整RNA修饰格局。

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