Cargando…

The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation

Plants produce new organs post-embryonically throughout their entire life cycle. This is due to stem cells present in the shoot and root apical meristems, the SAM and RAM, respectively. In the SAM, stem cells are located in the central zone where they divide slowly. Stem cell daughters are displaced...

Descripción completa

Detalles Bibliográficos
Autores principales: Bahafid, Elmehdi, Bradtmöller, Imke, Thies, Ann M, Nguyen, Thi TON, Gutierrez, Crisanto, Desvoyes, Bénédicte, Stahl, Yvonne, Blilou, Ikram, Simon, Rüdiger GW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642969/
https://www.ncbi.nlm.nih.gov/pubmed/37862096
http://dx.doi.org/10.7554/eLife.83334
_version_ 1785147056524886016
author Bahafid, Elmehdi
Bradtmöller, Imke
Thies, Ann M
Nguyen, Thi TON
Gutierrez, Crisanto
Desvoyes, Bénédicte
Stahl, Yvonne
Blilou, Ikram
Simon, Rüdiger GW
author_facet Bahafid, Elmehdi
Bradtmöller, Imke
Thies, Ann M
Nguyen, Thi TON
Gutierrez, Crisanto
Desvoyes, Bénédicte
Stahl, Yvonne
Blilou, Ikram
Simon, Rüdiger GW
author_sort Bahafid, Elmehdi
collection PubMed
description Plants produce new organs post-embryonically throughout their entire life cycle. This is due to stem cells present in the shoot and root apical meristems, the SAM and RAM, respectively. In the SAM, stem cells are located in the central zone where they divide slowly. Stem cell daughters are displaced laterally and enter the peripheral zone, where their mitotic activity increases and lateral organ primordia are formed. How the spatial arrangement of these different domains is initiated and controlled during SAM growth and development, and how sites of lateral organ primordia are determined in the peripheral zone is not yet completely understood. We found that the SHORTROOT (SHR) transcription factor together with its target transcription factors SCARECROW (SCR), SCARECROW-LIKE23 (SCL23) and JACKDAW (JKD), promotes formation of lateral organs and controls shoot meristem size. SHR, SCR, SCL23, and JKD are expressed in distinct, but partially overlapping patterns in the SAM. They can physically interact and activate expression of key cell cycle regulators such as CYCLIND6;1 (CYCD6;1) to promote the formation of new cell layers. In the peripheral zone, auxin accumulates at sites of lateral organ primordia initiation and activates SHR expression via the auxin response factor MONOPTEROS (MP) and auxin response elements in the SHR promoter. In the central zone, the SHR-target SCL23 physically interacts with the key stem cell regulator WUSCHEL (WUS) to promote stem cell fate. Both SCL23 and WUS expression are subject to negative feedback regulation from stem cells through the CLAVATA signaling pathway. Together, our findings illustrate how SHR-dependent transcription factor complexes act in different domains of the shoot meristem to mediate cell division and auxin dependent organ initiation in the peripheral zone, and coordinate this activity with stem cell maintenance in the central zone of the SAM.
format Online
Article
Text
id pubmed-10642969
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-106429692023-11-14 The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation Bahafid, Elmehdi Bradtmöller, Imke Thies, Ann M Nguyen, Thi TON Gutierrez, Crisanto Desvoyes, Bénédicte Stahl, Yvonne Blilou, Ikram Simon, Rüdiger GW eLife Developmental Biology Plants produce new organs post-embryonically throughout their entire life cycle. This is due to stem cells present in the shoot and root apical meristems, the SAM and RAM, respectively. In the SAM, stem cells are located in the central zone where they divide slowly. Stem cell daughters are displaced laterally and enter the peripheral zone, where their mitotic activity increases and lateral organ primordia are formed. How the spatial arrangement of these different domains is initiated and controlled during SAM growth and development, and how sites of lateral organ primordia are determined in the peripheral zone is not yet completely understood. We found that the SHORTROOT (SHR) transcription factor together with its target transcription factors SCARECROW (SCR), SCARECROW-LIKE23 (SCL23) and JACKDAW (JKD), promotes formation of lateral organs and controls shoot meristem size. SHR, SCR, SCL23, and JKD are expressed in distinct, but partially overlapping patterns in the SAM. They can physically interact and activate expression of key cell cycle regulators such as CYCLIND6;1 (CYCD6;1) to promote the formation of new cell layers. In the peripheral zone, auxin accumulates at sites of lateral organ primordia initiation and activates SHR expression via the auxin response factor MONOPTEROS (MP) and auxin response elements in the SHR promoter. In the central zone, the SHR-target SCL23 physically interacts with the key stem cell regulator WUSCHEL (WUS) to promote stem cell fate. Both SCL23 and WUS expression are subject to negative feedback regulation from stem cells through the CLAVATA signaling pathway. Together, our findings illustrate how SHR-dependent transcription factor complexes act in different domains of the shoot meristem to mediate cell division and auxin dependent organ initiation in the peripheral zone, and coordinate this activity with stem cell maintenance in the central zone of the SAM. eLife Sciences Publications, Ltd 2023-10-20 /pmc/articles/PMC10642969/ /pubmed/37862096 http://dx.doi.org/10.7554/eLife.83334 Text en © 2023, Bahafid et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Bahafid, Elmehdi
Bradtmöller, Imke
Thies, Ann M
Nguyen, Thi TON
Gutierrez, Crisanto
Desvoyes, Bénédicte
Stahl, Yvonne
Blilou, Ikram
Simon, Rüdiger GW
The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
title The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
title_full The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
title_fullStr The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
title_full_unstemmed The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
title_short The Arabidopsis SHORTROOT network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
title_sort arabidopsis shortroot network coordinates shoot apical meristem development with auxin-dependent lateral organ initiation
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642969/
https://www.ncbi.nlm.nih.gov/pubmed/37862096
http://dx.doi.org/10.7554/eLife.83334
work_keys_str_mv AT bahafidelmehdi thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT bradtmollerimke thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT thiesannm thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT nguyenthiton thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT gutierrezcrisanto thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT desvoyesbenedicte thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT stahlyvonne thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT blilouikram thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT simonrudigergw thearabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT bahafidelmehdi arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT bradtmollerimke arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT thiesannm arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT nguyenthiton arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT gutierrezcrisanto arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT desvoyesbenedicte arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT stahlyvonne arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT blilouikram arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation
AT simonrudigergw arabidopsisshortrootnetworkcoordinatesshootapicalmeristemdevelopmentwithauxindependentlateralorganinitiation