Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance

Arabidopsis Argonaute10 (AGO10) specifically sequesters miR165 and miR166 and antagonizes their activity, thus regulating shoot apical meristem (SAM) development. However, where and when this sequestration acts is currently unclear. We show here that AGO10 represses miR165/166 activity in the embryo...

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Main Authors: Yuyi Zhou, Minami Honda, Hongliang Zhu, Zhonghui Zhang, Xinwei Guo, Tianhong Li, Zhaohu Li, Xu Peng, Keiji Nakajima, Liusheng Duan, Xiuren Zhang
Format: Article
Language:English
Published: Elsevier 2015-03-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124715002053
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author Yuyi Zhou
Minami Honda
Hongliang Zhu
Zhonghui Zhang
Xinwei Guo
Tianhong Li
Zhaohu Li
Xu Peng
Keiji Nakajima
Liusheng Duan
Xiuren Zhang
author_facet Yuyi Zhou
Minami Honda
Hongliang Zhu
Zhonghui Zhang
Xinwei Guo
Tianhong Li
Zhaohu Li
Xu Peng
Keiji Nakajima
Liusheng Duan
Xiuren Zhang
author_sort Yuyi Zhou
collection DOAJ
description Arabidopsis Argonaute10 (AGO10) specifically sequesters miR165 and miR166 and antagonizes their activity, thus regulating shoot apical meristem (SAM) development. However, where and when this sequestration acts is currently unclear. We show here that AGO10 represses miR165/166 activity in the embryo proper during early embryogenesis, through the apical and central regions of mature embryos, and eventually in the entire adaxial domain and vasculature of the cotyledons and leaf primordia. These locations are essentially identical to regions expressing PHABULOSA and REVOLUTA, mRNA targets of miR165/166. The Arabidopsis genome contains nine MIR165/166 genes. Sequestration of miR165/166 by the MIR165b, MIR166a, MIR166b, and MIR166g promoters efficiently rescues the SAM defect in ago10 mutants. Comparison of the expression patterns of AGO10 and the four MIR165/166 members suggests that AGO10 quenches the non-cell-autonomous activity of any miR165/166 that moves into AGO10-expressing niches. Thus, this study provides insight into how the spatiotemporal regulation of AGO10-miR165/166 activity affects SAM development.
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spelling doaj.art-f364d2fb1ea54691ac91ccea2dc251022022-12-22T02:02:05ZengElsevierCell Reports2211-12472015-03-0110111819182710.1016/j.celrep.2015.02.047Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem MaintenanceYuyi Zhou0Minami Honda1Hongliang Zhu2Zhonghui Zhang3Xinwei Guo4Tianhong Li5Zhaohu Li6Xu Peng7Keiji Nakajima8Liusheng Duan9Xiuren Zhang10College of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, ChinaGraduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0192, JapanDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USADepartment of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USACollege of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, ChinaCollege of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, ChinaCollege of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, ChinaDepartment of Medical Physiology, Texas A&M University Health Science Center, Temple, TX 76504, USAGraduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0192, JapanCollege of Agriculture and Biotechnology, China Agricultural University, Beijing 100193, ChinaDepartment of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USAArabidopsis Argonaute10 (AGO10) specifically sequesters miR165 and miR166 and antagonizes their activity, thus regulating shoot apical meristem (SAM) development. However, where and when this sequestration acts is currently unclear. We show here that AGO10 represses miR165/166 activity in the embryo proper during early embryogenesis, through the apical and central regions of mature embryos, and eventually in the entire adaxial domain and vasculature of the cotyledons and leaf primordia. These locations are essentially identical to regions expressing PHABULOSA and REVOLUTA, mRNA targets of miR165/166. The Arabidopsis genome contains nine MIR165/166 genes. Sequestration of miR165/166 by the MIR165b, MIR166a, MIR166b, and MIR166g promoters efficiently rescues the SAM defect in ago10 mutants. Comparison of the expression patterns of AGO10 and the four MIR165/166 members suggests that AGO10 quenches the non-cell-autonomous activity of any miR165/166 that moves into AGO10-expressing niches. Thus, this study provides insight into how the spatiotemporal regulation of AGO10-miR165/166 activity affects SAM development.http://www.sciencedirect.com/science/article/pii/S2211124715002053
spellingShingle Yuyi Zhou
Minami Honda
Hongliang Zhu
Zhonghui Zhang
Xinwei Guo
Tianhong Li
Zhaohu Li
Xu Peng
Keiji Nakajima
Liusheng Duan
Xiuren Zhang
Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance
Cell Reports
title Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance
title_full Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance
title_fullStr Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance
title_full_unstemmed Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance
title_short Spatiotemporal Sequestration of miR165/166 by Arabidopsis Argonaute10 Promotes Shoot Apical Meristem Maintenance
title_sort spatiotemporal sequestration of mir165 166 by arabidopsis argonaute10 promotes shoot apical meristem maintenance
url http://www.sciencedirect.com/science/article/pii/S2211124715002053
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