Genome-wide high-resolution mapping of exosome substrates reveals hidden features in the Arabidopsis transcriptome

被引:270
作者
Chekanova, Julia A. [3 ,4 ]
Gregory, Brian D. [1 ,2 ]
Reverdatto, Sergei V. [4 ]
Chen, Huaming [2 ]
Kumar, Ravi [3 ]
Hooker, Tanya [3 ]
Yazaki, Junshi [1 ,2 ]
Li, Pinghua [4 ]
Skiba, Nikolai [5 ]
Peng, Qian [1 ,6 ]
Alonso, Jose [1 ]
Brukhin, Vladimir [7 ,8 ]
Grossniklaus, Ueli [7 ,8 ]
Ecker, Joseph R. [1 ,2 ]
Belostotsky, Dmitry A. [3 ,4 ]
机构
[1] Salk Inst Biol Studies, Plant Biol Lab, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Genome Anal Lab, La Jolla, CA 92037 USA
[3] Univ Missouri, Sch Biol Sci, Kansas City, MO 64110 USA
[4] SUNY Albany, Dept Biol Sci, Albany, NY 12222 USA
[5] Harvard Univ, Sch Med, Howe Lab Ophthalmol, Boston, MA 02114 USA
[6] Univ Calif San Diego, Dept Comp Sci & Engn, La Jolla, CA 92037 USA
[7] Univ Zurich, Inst Plant Biol, CH-8008 Zurich, Switzerland
[8] Univ Zurich, Zurich Basel Plant Sci Ctr, CH-8008 Zurich, Switzerland
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.cell.2007.10.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The exosome complex plays a central and essential role in RNA metabolism. However, comprehensive studies of exosome substrates and functional analyses of its subunits are lacking. Here, we demonstrate that as opposed to yeast and metazoans the plant exosome core possesses an unanticipated functional plasticity and present a genome-wide atlas of Arabidopsis exosome targets. Additionally, our study provides evidence for widespread polyadenylation- and exosome-mediated RNA quality control in plants, reveals unexpected aspects of stable structural RNA metabolism, and uncovers numerous novel exosome substrates. These include a select subset of mRNAs, miRNA processing intermediates, and hundreds of noncoding RNAs, the vast majority of which have not been previously described and belong to a layer of the transcriptome that can only be visualized upon inhibition of exosome activity. These first genome-wide maps of exosome substrates will aid in illuminating new fundamental components and regulatory mechanisms of eukaryotic transcriptomes.
引用
收藏
页码:1340 / 1353
页数:14
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