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Erecta 家族信号将 和 约束到茎尖分生组织的中心。

ERECTA family signaling constrains and to the center of the shoot apical meristem.

机构信息

Department of Biochemistry, Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, USA.

Beijing Advanced Innovation Center for Structural Biology, Tsinghua-Peking Joint Center for Life Sciences, Center for Plant Biology, School of Life Sciences, Tsinghua University, 100084 Beijing, China.

出版信息

Development. 2021 Mar 9;148(5):dev189753. doi: 10.1242/dev.189753.

Abstract

The shoot apical meristem (SAM) is a reservoir of stem cells that gives rise to all post-embryonic above-ground plant organs. The size of the SAM remains stable over time owing to a precise balance of stem cell replenishment versus cell incorporation into organ primordia. The WUSCHEL (WUS)/CLAVATA (CLV) negative feedback loop is central to SAM size regulation. Its correct function depends on accurate spatial expression of and A signaling pathway, consisting of ERECTA family (ERf) receptors and EPIDERMAL PATTERNING FACTOR LIKE (EPFL) ligands, restricts SAM width and promotes leaf initiation. Although ERf receptors are expressed throughout the SAM, EPFL ligands are expressed in its periphery. Our genetic analysis of demonstrated that ERfs and CLV3 synergistically regulate the size of the SAM, and is epistatic to ERf genes. Furthermore, activation of ERf signaling with exogenous EPFLs resulted in a rapid decrease of and expression. ERf-EPFL signaling inhibits expression of and in the periphery of the SAM, confining them to the center. These findings establish the molecular mechanism for stem cell positioning along the radial axis.

摘要

茎顶端分生组织(SAM)是干细胞的储存库,它产生所有胚胎后地上植物器官。由于干细胞补充与细胞并入器官原基之间的精确平衡,SAM 的大小保持稳定。WUSCHEL(WUS)/CLAVATA(CLV)负反馈环是 SAM 大小调节的核心。其正确功能取决于由 ERECTA 家族(ERf)受体和 EPIDERMAL PATTERNING FACTOR LIKE(EPFL)配体组成的和 A 信号通路的准确空间表达,限制 SAM 宽度并促进叶片起始。尽管 ERf 受体在整个 SAM 中表达,但 EPFL 配体在其外围表达。我们对的遗传分析表明,ERfs 和 CLV3 协同调节 SAM 的大小,并且对 ERf 基因具有上位性。此外,用外源 EPFLs 激活 ERf 信号导致和的表达迅速下降。ERf-EPFL 信号抑制 SAM 外围的和的表达,将它们限制在中心。这些发现确立了干细胞在径向轴上定位的分子机制。

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