Cargando…

Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana

Vegetative phase change is regulated by a decrease in the abundance of the miRNAs, miR156 and miR157, and the resulting increase in the expression of their targets, SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factors. To determine how miR156/miR157 specify the quantitative and qualita...

Descripción completa

Detalles Bibliográficos
Autores principales: He, Jia, Xu, Mingli, Willmann, Matthew R., McCormick, Kevin, Hu, Tieqiang, Yang, Li, Starker, Colby G., Voytas, Daniel F., Meyers, Blake C., Poethig, R. Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5929574/
https://www.ncbi.nlm.nih.gov/pubmed/29672610
http://dx.doi.org/10.1371/journal.pgen.1007337
_version_ 1783319433549185024
author He, Jia
Xu, Mingli
Willmann, Matthew R.
McCormick, Kevin
Hu, Tieqiang
Yang, Li
Starker, Colby G.
Voytas, Daniel F.
Meyers, Blake C.
Poethig, R. Scott
author_facet He, Jia
Xu, Mingli
Willmann, Matthew R.
McCormick, Kevin
Hu, Tieqiang
Yang, Li
Starker, Colby G.
Voytas, Daniel F.
Meyers, Blake C.
Poethig, R. Scott
author_sort He, Jia
collection PubMed
description Vegetative phase change is regulated by a decrease in the abundance of the miRNAs, miR156 and miR157, and the resulting increase in the expression of their targets, SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factors. To determine how miR156/miR157 specify the quantitative and qualitative changes in leaf morphology that occur during vegetative phase change, we measured their abundance in successive leaves and characterized the phenotype of mutations in different MIR156 and MIR157 genes. miR156/miR157 decline rapidly between leaf 1&2 and leaf 3 and decrease more slowly after this point. The amount of miR156/miR157 in leaves 1&2 greatly exceeds the threshold required to specify their identity. Subsequent leaves have relatively low levels of miR156/miR157 and are sensitive to small changes in their abundance. In these later-formed leaves, the amount of miR156/miR157 is close to the threshold required to specify juvenile vs. adult identity; a relatively small decrease in the abundance of miR156/157 in these leaves produces a disproportionately large increase in SPL proteins and a significant change in leaf morphology. miR157 is more abundant than miR156 but has a smaller effect on shoot morphology and SPL gene expression than miR156. This may be attributable to the inefficiency with which miR157 is loaded onto AGO1, as well as to the presence of an extra nucleotide at the 5' end of miR157 that is mis-paired in the miR157:SPL13 duplex. miR156 represses different targets by different mechanisms: it regulates SPL9 by a combination of transcript cleavage and translational repression and regulates SPL13 primarily by translational repression. Our results offer a molecular explanation for the changes in leaf morphology that occur during shoot development in Arabidopsis and provide new insights into the mechanism by which miR156 and miR157 regulate gene expression.
format Online
Article
Text
id pubmed-5929574
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-59295742018-05-11 Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana He, Jia Xu, Mingli Willmann, Matthew R. McCormick, Kevin Hu, Tieqiang Yang, Li Starker, Colby G. Voytas, Daniel F. Meyers, Blake C. Poethig, R. Scott PLoS Genet Research Article Vegetative phase change is regulated by a decrease in the abundance of the miRNAs, miR156 and miR157, and the resulting increase in the expression of their targets, SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factors. To determine how miR156/miR157 specify the quantitative and qualitative changes in leaf morphology that occur during vegetative phase change, we measured their abundance in successive leaves and characterized the phenotype of mutations in different MIR156 and MIR157 genes. miR156/miR157 decline rapidly between leaf 1&2 and leaf 3 and decrease more slowly after this point. The amount of miR156/miR157 in leaves 1&2 greatly exceeds the threshold required to specify their identity. Subsequent leaves have relatively low levels of miR156/miR157 and are sensitive to small changes in their abundance. In these later-formed leaves, the amount of miR156/miR157 is close to the threshold required to specify juvenile vs. adult identity; a relatively small decrease in the abundance of miR156/157 in these leaves produces a disproportionately large increase in SPL proteins and a significant change in leaf morphology. miR157 is more abundant than miR156 but has a smaller effect on shoot morphology and SPL gene expression than miR156. This may be attributable to the inefficiency with which miR157 is loaded onto AGO1, as well as to the presence of an extra nucleotide at the 5' end of miR157 that is mis-paired in the miR157:SPL13 duplex. miR156 represses different targets by different mechanisms: it regulates SPL9 by a combination of transcript cleavage and translational repression and regulates SPL13 primarily by translational repression. Our results offer a molecular explanation for the changes in leaf morphology that occur during shoot development in Arabidopsis and provide new insights into the mechanism by which miR156 and miR157 regulate gene expression. Public Library of Science 2018-04-19 /pmc/articles/PMC5929574/ /pubmed/29672610 http://dx.doi.org/10.1371/journal.pgen.1007337 Text en © 2018 He et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
He, Jia
Xu, Mingli
Willmann, Matthew R.
McCormick, Kevin
Hu, Tieqiang
Yang, Li
Starker, Colby G.
Voytas, Daniel F.
Meyers, Blake C.
Poethig, R. Scott
Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana
title Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana
title_full Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana
title_fullStr Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana
title_full_unstemmed Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana
title_short Threshold-dependent repression of SPL gene expression by miR156/miR157 controls vegetative phase change in Arabidopsis thaliana
title_sort threshold-dependent repression of spl gene expression by mir156/mir157 controls vegetative phase change in arabidopsis thaliana
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5929574/
https://www.ncbi.nlm.nih.gov/pubmed/29672610
http://dx.doi.org/10.1371/journal.pgen.1007337
work_keys_str_mv AT hejia thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT xumingli thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT willmannmatthewr thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT mccormickkevin thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT hutieqiang thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT yangli thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT starkercolbyg thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT voytasdanielf thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT meyersblakec thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana
AT poethigrscott thresholddependentrepressionofsplgeneexpressionbymir156mir157controlsvegetativephasechangeinarabidopsisthaliana