Cargando…

Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities

The shoot meristem, a stem-cell-containing tissue initiated during plant embryogenesis, is responsible for continuous shoot organ production in postembryonic development. Although key regulatory factors including KNOX genes are responsible for stem cell maintenance in the shoot meristem, how the ons...

Descripción completa

Detalles Bibliográficos
Autores principales: Aida, Mitsuhiro, Tsubakimoto, Yuka, Shimizu, Satoko, Ogisu, Hiroyuki, Kamiya, Masako, Iwamoto, Ryosuke, Takeda, Seiji, Karim, Md Rezaul, Mizutani, Masaharu, Lenhard, Michael, Tasaka, Masao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461597/
https://www.ncbi.nlm.nih.gov/pubmed/32824181
http://dx.doi.org/10.3390/ijms21165864
_version_ 1783576769963491328
author Aida, Mitsuhiro
Tsubakimoto, Yuka
Shimizu, Satoko
Ogisu, Hiroyuki
Kamiya, Masako
Iwamoto, Ryosuke
Takeda, Seiji
Karim, Md Rezaul
Mizutani, Masaharu
Lenhard, Michael
Tasaka, Masao
author_facet Aida, Mitsuhiro
Tsubakimoto, Yuka
Shimizu, Satoko
Ogisu, Hiroyuki
Kamiya, Masako
Iwamoto, Ryosuke
Takeda, Seiji
Karim, Md Rezaul
Mizutani, Masaharu
Lenhard, Michael
Tasaka, Masao
author_sort Aida, Mitsuhiro
collection PubMed
description The shoot meristem, a stem-cell-containing tissue initiated during plant embryogenesis, is responsible for continuous shoot organ production in postembryonic development. Although key regulatory factors including KNOX genes are responsible for stem cell maintenance in the shoot meristem, how the onset of such factors is regulated during embryogenesis is elusive. Here, we present evidence that the two KNOX genes STM and KNAT6 together with the two other regulatory genes BLR and LAS are functionally important downstream genes of CUC1 and CUC2, which are a redundant pair of genes that specify the embryonic shoot organ boundary. Combined expression of STM with any of KNAT6, BLR, and LAS can efficiently rescue the defects of shoot meristem formation and/or separation of cotyledons in cuc1 cuc2 double mutants. In addition, CUC1 and CUC2 are also required for the activation of KLU, a cytochrome P450-encoding gene known to restrict organ production, and KLU counteracts STM in the promotion of meristem activity, providing a possible balancing mechanism for shoot meristem maintenance. Together, these results establish the roles for CUC1 and CUC2 in coordinating the activation of two classes of genes with opposite effects on shoot meristem activity.
format Online
Article
Text
id pubmed-7461597
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-74615972020-09-04 Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities Aida, Mitsuhiro Tsubakimoto, Yuka Shimizu, Satoko Ogisu, Hiroyuki Kamiya, Masako Iwamoto, Ryosuke Takeda, Seiji Karim, Md Rezaul Mizutani, Masaharu Lenhard, Michael Tasaka, Masao Int J Mol Sci Article The shoot meristem, a stem-cell-containing tissue initiated during plant embryogenesis, is responsible for continuous shoot organ production in postembryonic development. Although key regulatory factors including KNOX genes are responsible for stem cell maintenance in the shoot meristem, how the onset of such factors is regulated during embryogenesis is elusive. Here, we present evidence that the two KNOX genes STM and KNAT6 together with the two other regulatory genes BLR and LAS are functionally important downstream genes of CUC1 and CUC2, which are a redundant pair of genes that specify the embryonic shoot organ boundary. Combined expression of STM with any of KNAT6, BLR, and LAS can efficiently rescue the defects of shoot meristem formation and/or separation of cotyledons in cuc1 cuc2 double mutants. In addition, CUC1 and CUC2 are also required for the activation of KLU, a cytochrome P450-encoding gene known to restrict organ production, and KLU counteracts STM in the promotion of meristem activity, providing a possible balancing mechanism for shoot meristem maintenance. Together, these results establish the roles for CUC1 and CUC2 in coordinating the activation of two classes of genes with opposite effects on shoot meristem activity. MDPI 2020-08-15 /pmc/articles/PMC7461597/ /pubmed/32824181 http://dx.doi.org/10.3390/ijms21165864 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Aida, Mitsuhiro
Tsubakimoto, Yuka
Shimizu, Satoko
Ogisu, Hiroyuki
Kamiya, Masako
Iwamoto, Ryosuke
Takeda, Seiji
Karim, Md Rezaul
Mizutani, Masaharu
Lenhard, Michael
Tasaka, Masao
Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities
title Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities
title_full Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities
title_fullStr Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities
title_full_unstemmed Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities
title_short Establishment of the Embryonic Shoot Meristem Involves Activation of Two Classes of Genes with Opposing Functions for Meristem Activities
title_sort establishment of the embryonic shoot meristem involves activation of two classes of genes with opposing functions for meristem activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461597/
https://www.ncbi.nlm.nih.gov/pubmed/32824181
http://dx.doi.org/10.3390/ijms21165864
work_keys_str_mv AT aidamitsuhiro establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT tsubakimotoyuka establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT shimizusatoko establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT ogisuhiroyuki establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT kamiyamasako establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT iwamotoryosuke establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT takedaseiji establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT karimmdrezaul establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT mizutanimasaharu establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT lenhardmichael establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities
AT tasakamasao establishmentoftheembryonicshootmeristeminvolvesactivationoftwoclassesofgeneswithopposingfunctionsformeristemactivities