首页> 外文期刊>Nucleic acids research >Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution
【24h】

Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution

机译:在archaea中核糖体剖面揭示了单个密码子分辨率的无线翻译,新颖的翻译启动位点和核糖体暂停

获取原文
           

摘要

High-throughput methods, such as ribosome profiling, have revealed the complexity of translation regulation in Bacteria and Eukarya with large-scale effects on cellular functions. In contrast, the translational landscape in Archaea remains mostly unexplored. Here, we developed ribosome profiling in a model archaeon, Haloferax volcanii, elucidating, for the first time, the translational landscape of a representative of the third domain of life. We determined the ribosome footprint of H. volcanii to be comparable in size to that of the Eukarya. We linked footprint lengths to initiating and elongating states of the ribosome on leadered transcripts, operons, and on leaderless transcripts, the latter representing 70% of H. volcanii transcriptome. We manipulated ribosome activity with translation inhibitors to reveal ribosome pausing at specific codons. Lastly, we found that the drug harringtonine arrested ribosomes at initiation sites in this archaeon. This drug treatment allowed us to confirm known translation initiation sites and also reveal putative novel initiation sites in intergenic regions and within genes. Ribosome profiling revealed an uncharacterized complexity of translation in this archaeon with bacteria-like, eukarya-like, and potentially novel translation mechanisms. These mechanisms are likely to be functionally essential and to contribute to an expanded proteome with regulatory roles in gene expression.
机译:高通量方法,如核糖体分析,揭示了细菌和Eukarya中翻译调节的复杂性,对细胞功能大规模影响。相比之下,Archaea中的翻译景观仍然是未开发的。在这里,我们开发了核糖体谱在古典群岛,哈福克斯·沃尔卡利,阐明了第三领域的第三领域代表的翻译景观。我们确定了H. Volcanii的核糖体足迹与Eukarya的大小相当。我们将足迹长度连接到核糖体的引发和伸长核糖体的状态,并在下后的转录物上和无线转录物上,其代表70%的H. Volcanii转录组。我们用翻译抑制剂操纵核糖体活性,以显示在特定密码子上暂停的核糖体。最后,我们发现该药物Harringtonine在该古老的群体的起始位点被捕核糖体。该药物治疗使我们能够确认已知的翻译引发位点,并揭示了基因内和基因内的推定新的起始位点。核糖体剖面揭示了这种古老的古顿的翻译复杂性,含有细菌,真核状物,似的似的翻译机制。这些机制可能是在功能上必需的,并有助于扩张的蛋白质组,具有基因表达中具有调节作用的蛋白质组。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号