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      Atlas of Subcellular RNA Localization Revealed by APEX-seq

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          SUMMARY

          We introduce APEX-seq, a method for RNA sequencing based on direct proximity labeling of RNA using the peroxidase enzyme APEX2. APEX-seq in nine distinct subcellular locales produced a nanometer-resolution spatial map of the human transcriptome as a resource, revealing extensive patterns of localization for diverse RNA classes and transcript isoforms. We uncover a radial organization of the nuclear transcriptome, which is gated at the inner surface of the nuclear pore for cytoplasmic export of processed transcripts. We identify two distinct pathways of messenger RNA localization to mitochondria, each associated with specific sets of transcripts for building complementary macromolecular machines within the organelle. APEX-seq should be widely applicable to many systems, enabling comprehensive investigations of the spatial transcriptome.

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          1-sentence summary

          A newly-developed technique reveals the subcellular transcriptomes at many landmarks in the nucleus and cytosol, and connects mRNA localization to genome architecture, protein location and local-translation mechanisms.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          22 August 2019
          20 June 2019
          11 July 2019
          11 July 2020
          : 178
          : 2
          : 473-490.e26
          Affiliations
          [1 ]Center for Personal Dynamics Regulomes, Stanford University School of Medicine, Stanford, CA 94305, USA
          [2 ]Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305, USA
          [3 ]Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA
          [4 ]Department of Chemistry, Stanford University, Stanford, CA 94305, USA
          [5 ]Department of Biology, Stanford University, Stanford, CA 94305, USA
          [6 ]Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
          [7 ]Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA
          [8 ]Chan Zuckerberg Biohub, San Francisco, CA 94158, USA
          [9 ]These authors contributed equally
          [10 ]These authors contributed equally
          [11 ]Lead contact
          Author notes

          AUTHOR CONTRIBUTIONS

          F.M.F., P.K., H.Y.C and A.Y.T. conceived the project. F.M.F., S.H., P.K., H.Y.C. and A.Y.T. designed experiments. F.M.F., S.H. and P.K. performed all experiments, unless otherwise noted. F.M.F. designed and carried out sequencing experiments. S.H., A.N.B. and A.Y.T. designed and carried out sequential FISH experiments. F.M.F, S.H, K.R.P., P.K, J.X. and A.Y.T. analyzed data. F.M.F., S.H., H.Y.C. and A.Y.T. wrote the paper with input from all authors. H.Y.C. and A.Y.T. jointly supervised work and acquired funding.

          [* ]Correspondence: ayting@ 123456stanford.edu (A.Y.T.); howchang@ 123456stanford.edu (H.Y.C.)
          Article
          PMC6786773 PMC6786773 6786773 nihpa1531987
          10.1016/j.cell.2019.05.027
          6786773
          31230715
          fbdaa11e-7f20-4126-99d5-a167554cb091
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