Translational Control of Cell Division by Elongator
Elongator is required for the synthesis of the mcm5s2 modification found on tRNAs recognizing AA-ending codons. In order to obtain a global picture of the role of Elongator in translation, we used reverse protein arrays to screen the fission yeast proteome for translation defects. Unexpectedly, thi...
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doaj-d3cc08f0338e46799bb1ad68f92e15ba2020-11-25T02:29:00ZengElsevierCell Reports2211-12472012-05-011542443310.1016/j.celrep.2012.04.001Translational Control of Cell Division by ElongatorFanelie Bauer0Akihisa Matsuyama1Julie Candiracci2Marc Dieu3Judith Scheliga4Dieter A. Wolf5Minoru Yoshida6Damien Hermand7Namur Research College (NARC), The University of Namur, Namur 5000, BelgiumChemical Genetics Laboratory, RIKEN Advanced Science Institute, Wako, Saitama 351-0198, JapanNamur Research College (NARC), The University of Namur, Namur 5000, BelgiumSpectrometrie de Masse, The University of Namur, Namur 5000, BelgiumStanford-Burnham Medical Research, La Jolla, CA 92037, USAStanford-Burnham Medical Research, La Jolla, CA 92037, USAChemical Genetics Laboratory, RIKEN Advanced Science Institute, Wako, Saitama 351-0198, JapanNamur Research College (NARC), The University of Namur, Namur 5000, Belgium Elongator is required for the synthesis of the mcm5s2 modification found on tRNAs recognizing AA-ending codons. In order to obtain a global picture of the role of Elongator in translation, we used reverse protein arrays to screen the fission yeast proteome for translation defects. Unexpectedly, this revealed that Elongator inactivation mainly affected three specific functional groups including proteins implicated in cell division. The absence of Elongator results in a delay in mitosis onset and cytokinesis defects. We demonstrate that the kinase Cdr2, which is a central regulator of mitosis and cytokinesis, is under translational control by Elongator due to the Lysine codon usage bias of the cdr2 coding sequence. These findings uncover a mechanism by which the codon usage, coupled to tRNA modifications, fundamentally contributes to gene expression and cellular functions. http://www.sciencedirect.com/science/article/pii/S2211124712001143 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fanelie Bauer Akihisa Matsuyama Julie Candiracci Marc Dieu Judith Scheliga Dieter A. Wolf Minoru Yoshida Damien Hermand |
spellingShingle |
Fanelie Bauer Akihisa Matsuyama Julie Candiracci Marc Dieu Judith Scheliga Dieter A. Wolf Minoru Yoshida Damien Hermand Translational Control of Cell Division by Elongator Cell Reports |
author_facet |
Fanelie Bauer Akihisa Matsuyama Julie Candiracci Marc Dieu Judith Scheliga Dieter A. Wolf Minoru Yoshida Damien Hermand |
author_sort |
Fanelie Bauer |
title |
Translational Control of Cell Division by Elongator |
title_short |
Translational Control of Cell Division by Elongator |
title_full |
Translational Control of Cell Division by Elongator |
title_fullStr |
Translational Control of Cell Division by Elongator |
title_full_unstemmed |
Translational Control of Cell Division by Elongator |
title_sort |
translational control of cell division by elongator |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2012-05-01 |
description |
Elongator is required for the synthesis of the mcm5s2 modification found on tRNAs recognizing AA-ending codons. In order to obtain a global picture of the role of Elongator in translation, we used reverse protein arrays to screen the fission yeast proteome for translation defects. Unexpectedly, this revealed that Elongator inactivation mainly affected three specific functional groups including proteins implicated in cell division. The absence of Elongator results in a delay in mitosis onset and cytokinesis defects. We demonstrate that the kinase Cdr2, which is a central regulator of mitosis and cytokinesis, is under translational control by Elongator due to the Lysine codon usage bias of the cdr2 coding sequence. These findings uncover a mechanism by which the codon usage, coupled to tRNA modifications, fundamentally contributes to gene expression and cellular functions.
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url |
http://www.sciencedirect.com/science/article/pii/S2211124712001143 |
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