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      Analyses of mRNA structure dynamics identify embryonic gene regulatory programs

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          Abstract

          RNA folding plays a crucial role in RNA function. However, knowledge of the global structure of the transcriptome is limited to cellular systems at steady state, thus hindering the understanding of RNA structure dynamics during biological transitions and how it influences gene function. Here, we characterized mRNA structure dynamics during zebrafish development. We observed that on a global level, translation guides structure rather than structure guiding translation. We detected a decrease in structure in translated regions and identified the ribosome as a major remodeler of RNA structure in vivo. In contrast, we found that 3’ untranslated regions (UTRs) form highly folded structures in vivo, which can affect gene expression by modulating microRNA activity. Furthermore, dynamic 3’-UTR structures contain RNA-decay elements, such as the regulatory elements in nanog and ccna1, two genes encoding key maternal factors orchestrating the maternal-to-zygotic transition. These results reveal a central role of RNA structure dynamics in gene regulatory programs.

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          Most cited references38

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          eIF4 initiation factors: effectors of mRNA recruitment to ribosomes and regulators of translation.

          Eukaryotic translation initiation factor 4F (eIF4F) is a protein complex that mediates recruitment of ribosomes to mRNA. This event is the rate-limiting step for translation under most circumstances and a primary target for translational control. Functions of the constituent proteins of eIF4F include recognition of the mRNA 5' cap structure (eIF4E), delivery of an RNA helicase to the 5' region (eIF4A), bridging of the mRNA and the ribosome (eIF4G), and circularization of the mRNA via interaction with poly(A)-binding protein (eIF4G). eIF4 activity is regulated by transcription, phosphorylation, inhibitory proteins, and proteolytic cleavage. Extracellular stimuli evoke changes in phosphorylation that influence eIF4F activity, especially through the phosphoinositide 3-kinase (PI3K) and Ras signaling pathways. Viral infection and cellular stresses also affect eIF4F function. The recent determination of the structure of eIF4E at atomic resolution has provided insight about how translation is initiated and regulated. Evidence suggests that eIF4F is also implicated in malignancy and apoptosis.
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            Poly(A)-tail profiling reveals an embryonic switch in translational control

            Poly(A) tails enhance the stability and translation of most eukaryotic mRNAs, but difficulties in globally measuring poly(A)-tail lengths have impeded greater understanding of poly(A)-tail function. Here, we describe poly(A)-tail length profiling by sequencing (PAL-seq) and apply it to measure tail lengths of millions of individual RNAs isolated from yeasts, cell lines, Arabidopsis leaves, mouse liver, and zebrafish and frog embryos. Poly(A)-tail lengths were conserved between orthologous mRNAs, with mRNAs encoding ribosomal proteins and other “housekeeping” proteins tending to have shorter tails. As expected, tail lengths were coupled to translational efficiency in early zebrafish and frog embryos. However, this strong coupling diminished at gastrulation and was absent in non-embryonic samples, indicating a rapid developmental switch in the nature of translational control. This switch complements an earlier switch to zygotic transcriptional control and explains why the predominant effect of microRNA-mediated deadenylation concurrently shifts from translational repression to mRNA destabilization.
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              Ribosome profiling shows that miR-430 reduces translation before causing mRNA decay in zebrafish.

              MicroRNAs regulate gene expression through deadenylation, repression, and messenger RNA (mRNA) decay. However, the contribution of each mechanism in non-steady-state situations remains unclear. We monitored the impact of miR-430 on ribosome occupancy of endogenous mRNAs in wild-type and dicer mutant zebrafish embryos and found that miR-430 reduces the number of ribosomes on target mRNAs before causing mRNA decay. Translational repression occurs before complete deadenylation, and disrupting deadenylation with use of an internal polyadenylate tail did not block target repression. Lastly, we observed that ribosome density along the length of the message remains constant, suggesting that translational repression occurs by reducing the rate of initiation rather than affecting elongation or causing ribosomal drop-off. These results show that miR-430 regulates translation initiation before inducing mRNA decay during zebrafish development.
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                Author and article information

                Journal
                101186374
                31761
                Nat Struct Mol Biol
                Nat. Struct. Mol. Biol.
                Nature structural & molecular biology
                1545-9993
                1545-9985
                30 July 2019
                30 July 2018
                August 2018
                12 August 2019
                : 25
                : 8
                : 677-686
                Affiliations
                [1 ]Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
                [2 ]Computer Science and Electrical Engineering Department, Massachusetts Institute of Technology, Cambridge, MA, USA.
                [3 ]The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
                [4 ]Department of Neuroscience, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
                [5 ]School of Medicine, University of New South Wales, Sydney, New South Wales, Australia.
                [6 ]College of Arts and Sciences, University of New Haven, West Haven, CT, USA.
                [7 ]Yale Stem Cell Center, Yale University School of Medicine, New Haven, CT, USA.
                [8 ]These authors contributed equally: Jean-Denis Beaudoin, Eva Maria Novoa.
                Author notes

                Author contributions

                J.-D.B. and A.J.G. conceived the project. J.-D.B. performed the experiments. J.-D.B., E.M.N. and C.E.V. performed data processing. V.Y. identified the regulatory element in the nanog 3′ UTR and built the reporter constructs. C.M.T. performed the KHSRP iCLIP experiment. J.-D.B. and E.M.N. performed data analysis and, together with A.J.G., interpreted the results. A.J.G. supervised the project, with the contribution of M.K. J.-D.B., E.M.N. and A.J.G. wrote the manuscript with input from the other authors.

                [* ] Correspondence and requests for materials should be addressed to J.-D.B. or A.J.G. jean-denis.beaudoin@ 123456yale.edu ; antonio.giraldez@ 123456yale.edu
                Author information
                http://orcid.org/0000-0003-4932-1668
                http://orcid.org/0000-0002-7132-4534
                http://orcid.org/0000-0002-6823-137X
                Article
                PMC6690192 PMC6690192 6690192 nihpa1041242
                10.1038/s41594-018-0091-z
                6690192
                30061596
                6e38752b-935b-47e8-8ef2-33d27c109c85

                Reprints and permissions information is available at www.nature.com/reprints.

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