Arabidopsis Argonaute10 Specifically Sequesters miR166/165 to Regulate Shoot Apical Meristem Development
The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III HOMEODOMAIN-LEUCINE ZIPPER ( HD-ZIP III) transcription factors, which are targets of miR166/165. In Arabid...
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| Published in: | Cell Vol. 145; no. 2; pp. 242 - 256 |
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| Main Authors: | , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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Elsevier Inc
15-04-2011
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| Abstract | The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III
HOMEODOMAIN-LEUCINE ZIPPER (
HD-ZIP III) transcription factors, which are targets of miR166/165. In
Arabidopsis,
AGO10 is a critical regulator of SAM maintenance, and here we demonstrate that AGO10 specifically interacts with miR166/165. The association is determined by a distinct structure of the miR166/165 duplex. Deficient loading of miR166 into AGO10 results in a defective SAM. Notably, the miRNA-binding ability of AGO10, but not its catalytic activity, is required for SAM development, and AGO10 has a higher binding affinity for miR166 than does AGO1, a principal contributor to miRNA-mediated silencing. We propose that AGO10 functions as a decoy for miR166/165 to maintain the SAM, preventing their incorporation into AGO1 complexes and the subsequent repression of
HD-ZIP III gene expression.
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Arabidopsis AGO10 predominantly associates with miR166/165 ► The duplex structure of miR166/165 determines their specific association with AGO10 ► AGO10 competes with AGO1 for miR166/165 binding ► The decoy activity of AGO10 drives shoot apical meristem development |
|---|---|
| AbstractList | The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III
HOMEODOMAIN-LEUCINE ZIPPER (
HD-ZIP III) transcription factors, which are targets of miR166/165. In
Arabidopsis,
AGO10 is a critical regulator of SAM maintenance, and here we demonstrate that AGO10 specifically interacts with miR166/165. The association is determined by a distinct structure of the miR166/165 duplex. Deficient loading of miR166 into AGO10 results in a defective SAM. Notably, the miRNA-binding ability of AGO10, but not its catalytic activity, is required for SAM development, and AGO10 has a higher binding affinity for miR166 than does AGO1, a principal contributor to miRNA-mediated silencing. We propose that AGO10 functions as a decoy for miR166/165 to maintain the SAM, preventing their incorporation into AGO1 complexes and the subsequent repression of
HD-ZIP III gene expression.
[Display omitted]
[Display omitted]
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Arabidopsis AGO10 predominantly associates with miR166/165 ► The duplex structure of miR166/165 determines their specific association with AGO10 ► AGO10 competes with AGO1 for miR166/165 binding ► The decoy activity of AGO10 drives shoot apical meristem development The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III HOMEODOMAIN-LEUCINE ZIPPER (HD-ZIP III) transcription factors, which are targets of miR166/165. In Arabidopsis, AGO10 is a critical regulator of SAM maintenance, and here we demonstrate that AGO10 specifically interacts with miR166/165. The association is determined by a distinct structure of the miR166/165 duplex. Deficient loading of miR166 into AGO10 results in a defective SAM. Notably, the miRNA-binding ability of AGO10, but not its catalytic activity, is required for SAM development, and AGO10 has a higher binding affinity for miR166 than does AGO1, a principal contributor to miRNA-mediated silencing. We propose that AGO10 functions as a decoy for miR166/165 to maintain the SAM, preventing their incorporation into AGO1 complexes and the subsequent repression of HD-ZIP III gene expression. The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III HOMEODOMAIN-LEUCINE ZIPPER (HD-ZIP III) transcription factors, which are targets of miR166/165. In Arabidopsis, AGO10 is a critical regulator of SAM maintenance, and here we demonstrate that AGO10 specifically interacts with miR166/165. The association is determined by a distinct structure of the miR166/165 duplex. Deficient loading of miR166 into AGO10 results in a defective SAM. Notably, the miRNA-binding ability of AGO10, but not its catalytic activity, is required for SAM development, and AGO10 has a higher binding affinity for miR166 than does AGO1, a principal contributor to miRNA-mediated silencing. We propose that AGO10 functions as a decoy for miR166/165 to maintain the SAM, preventing their incorporation into AGO1 complexes and the subsequent repression of HD-ZIP III gene expression. |
| Author | Hu, Fuqu Zhu, Hongliang Barefoot, Ashley Wang, Ronghui Sze, Sing-Hoi Liou, Lisa Wen Zhang, Xiuren Zhou, Xin Dickman, Martin |
| Author_xml | – sequence: 1 givenname: Hongliang surname: Zhu fullname: Zhu, Hongliang organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA – sequence: 2 givenname: Fuqu surname: Hu fullname: Hu, Fuqu organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA – sequence: 3 givenname: Ronghui surname: Wang fullname: Wang, Ronghui organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA – sequence: 4 givenname: Xin surname: Zhou fullname: Zhou, Xin organization: Institute for Plant Genomics and Biotechnology, Texas A&M University, College Station, TX 77843, USA – sequence: 5 givenname: Sing-Hoi surname: Sze fullname: Sze, Sing-Hoi organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA – sequence: 6 givenname: Lisa Wen surname: Liou fullname: Liou, Lisa Wen organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA – sequence: 7 givenname: Ashley surname: Barefoot fullname: Barefoot, Ashley organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA – sequence: 8 givenname: Martin surname: Dickman fullname: Dickman, Martin organization: Institute for Plant Genomics and Biotechnology, Texas A&M University, College Station, TX 77843, USA – sequence: 9 givenname: Xiuren surname: Zhang fullname: Zhang, Xiuren email: xiuren.zhang@tamu.edu organization: Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USA |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/21496644$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | apical meristems Arabidopsis Arabidopsis - genetics Arabidopsis - growth & development Arabidopsis - metabolism Arabidopsis Proteins - metabolism Argonaute Proteins binding capacity catalytic activity gene expression Gene Expression Regulation, Plant Meristem - growth & development MicroRNAs - genetics Plant Shoots RNA, Plant - genetics transcription factors |
| Title | Arabidopsis Argonaute10 Specifically Sequesters miR166/165 to Regulate Shoot Apical Meristem Development |
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