Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published October 5, 2010 | Supplemental Material + Published
Journal Article Open

Cell-type specific analysis of translating RNAs in developing flowers reveals new levels of control

Abstract

Determining both the expression levels of mRNA and the regulation of its translation is important in understanding specialized cell functions. In this study, we describe both the expression profiles of cells within spatiotemporal domains of the Arabidopsis thaliana flower and the post-transcriptional regulation of these mRNAs, at nucleotide resolution. We express a tagged ribosomal protein under the promoters of three master regulators of flower development. By precipitating tagged polysomes, we isolated cell type specific mRNAs that are probably translating, and quantified those mRNAs through deep sequencing. Cell type comparisons identified known cell-specific transcripts and uncovered many new ones, from which we inferred cell type-specific hormone responses, promoter motifs and coexpressed cognate binding factor candidates, and splicing isoforms. By comparing translating mRNAs with steady-state overall transcripts, we found evidence for widespread post-transcriptional regulation at both the intron splicing and translational stages. Sequence analyses identified structural features associated with each step. Finally, we identified a new class of noncoding RNAs associated with polysomes. Findings from our profiling lead to new hypotheses in the understanding of flower development.

Additional Information

© 2010 EMBO and Macmillan Publishers Limited. Molecular Systems Biology is an open-access journal published by European Molecular Biology Organization and Nature Publishing Group. This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License. Received 19.3.10; accepted 27.8.2010. published online 5 October 2010. We thank J Bailey-Serres, T Laux, I Moore, and F Wellmer for seeds and constructs; X Zhang and S-O Shan for invaluable help during polysome isolation; A Mortazavi, B Williams, B Wold, and H Jiang for advice on deep sequencing and data processing; H Amrhein, L Schaeffer, and D Trout for professional technical assistance; and W Li, A Roeder, K Sugimoto, and other members of the Meyerowitz lab for comments on the paper. This study was supported by the Edelman Discovery Fund of the California Institute of Technology (CIT) to EMM, by NSF 2010 Project grant MCB-0929349 to EMM and YJ, and by the Millard and Muriel Jacobs Genetics and Genomics Laboratory at CIT. The authors declare that they have no conflict of interest.

Attached Files

Published - Jiao2010p11970Mol_Syst_Biol.pdf

Supplemental Material - msb201076-s1.pdf

Supplemental Material - msb201076-s2.xls

Files

Jiao2010p11970Mol_Syst_Biol.pdf
Files (50.7 MB)
Name Size Download all
md5:cf8980dc8d2450fe80ca63ecab0d93b3
2.6 MB Preview Download
md5:83dd8fe81e4030203153959a3a71c2e9
1.4 MB Preview Download
md5:1378e52a7fe0c578179249a98bca6efe
46.7 MB Download

Additional details

Created:
August 22, 2023
Modified:
October 20, 2023