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      Assembly and functionality of the ribosome with tethered subunits

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          Abstract

          Ribo-T is an engineered ribosome whose small and large subunits are tethered together by linking 16S rRNA and 23S rRNA in a single molecule. Although Ribo-T can support cell proliferation in the absence of wild type ribosomes, Ribo-T cells grow slower than those with wild type ribosomes. Here, we show that cell growth defect is likely explained primarily by slow Ribo-T assembly rather than its imperfect functionality. Ribo-T maturation is stalled at a late assembly stage. Several post-transcriptional rRNA modifications and some ribosomal proteins are underrepresented in the accumulated assembly intermediates and rRNA ends are incompletely trimmed. Ribosome profiling of Ribo-T cells shows no defects in translation elongation but reveals somewhat higher occupancy by Ribo-T of the start codons and to a lesser extent stop codons, suggesting that subunit tethering mildly affects the initiation and termination stages of translation. Understanding limitations of Ribo-T system offers ways for its future development.

          Abstract

          The tethered ribosome system Ribo-T supports cell proliferation though at a reduced rate. Here the authors show this is due to slower ribosome assembly instead of reduced functionality.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            The structural basis of ribosome activity in peptide bond synthesis.

            Using the atomic structures of the large ribosomal subunit from Haloarcula marismortui and its complexes with two substrate analogs, we establish that the ribosome is a ribozyme and address the catalytic properties of its all-RNA active site. Both substrate analogs are contacted exclusively by conserved ribosomal RNA (rRNA) residues from domain V of 23S rRNA; there are no protein side-chain atoms closer than about 18 angstroms to the peptide bond being synthesized. The mechanism of peptide bond synthesis appears to resemble the reverse of the acylation step in serine proteases, with the base of A2486 (A2451 in Escherichia coli) playing the same general base role as histidine-57 in chymotrypsin. The unusual pK(a) (where K(a) is the acid dissociation constant) required for A2486 to perform this function may derive in part from its hydrogen bonding to G2482 (G2447 in E. coli), which also interacts with a buried phosphate that could stabilize unusual tautomers of these two bases. The polypeptide exit tunnel is largely formed by RNA but has significant contributions from proteins L4, L22, and L39e, and its exit is encircled by proteins L19, L22, L23, L24, L29, and L31e.
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              Transcriptome-wide measurement of translation by ribosome profiling

              Translation is one of the fundamental processes of life. It comprises the assembly of polypeptides whose amino acid sequence corresponds to the codon sequence of an mRNA's ORF. Translation is performed by the ribosome; therefore, in order to understand translation and its regulation we must be able to determine the numbers and locations of ribosomes on mRNAs in vivo. Furthermore, we must be able to examine their redistribution in different physiological contexts and in response to experimental manipulations. The ribosome profiling method provides us with an opportunity to learn these locations, by sequencing a cDNA library derived from the short fragments of mRNA covered by the ribosome. Since its original description, the ribosome profiling method has undergone continuing development; in this article we describe the method's current state. Important improvements include: the incorporation of sample barcodes to enable library multiplexing, the incorporation of unique molecular identifiers to enable to removal of duplicated sequences, and the replacement of a gel-purification step with the enzymatic degradation of unligated linker.
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                Author and article information

                Contributors
                jaanus.remme@ut.ee
                shura@uic.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                25 February 2019
                25 February 2019
                2019
                : 10
                : 930
                Affiliations
                [1 ]ISNI 0000 0001 2175 0319, GRID grid.185648.6, Center for Biomolecular Sciences, , University of Illinois at Chicago, ; Chicago, IL 60607 USA
                [2 ]ISNI 0000 0001 0943 7661, GRID grid.10939.32, Institute of Molecular and Cell Biology, , University of Tartu, ; Riia 23, 51010 Tartu, Estonia
                [3 ]ISNI 0000 0001 2299 3507, GRID grid.16753.36, Department of Chemical and Biological Engineering and Center for Synthetic Biology, , Northwestern University, ; 2145 Sheridan Road, Evanston, IL 60208 USA
                [4 ]ISNI 0000 0004 1936 9924, GRID grid.89336.37, Present Address: Department of Integrative Biology, Institute for Cellular and Molecular Biology, , The University of Texas at Austin, ; 2500 Speedway, Austin, TX 78712 USA
                Author information
                http://orcid.org/0000-0002-3403-7587
                http://orcid.org/0000-0001-9476-0104
                http://orcid.org/0000-0003-2256-693X
                http://orcid.org/0000-0003-2948-6211
                http://orcid.org/0000-0002-3301-827X
                Article
                8892
                10.1038/s41467-019-08892-w
                6389949
                30804338
                100caaa8-2a7f-420c-963f-f1fde20f60c4
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 August 2018
                : 25 January 2019
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