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表面定位糖蛋白通过 C 类 ARF 调节Physcomitrium patens 原丝体的起始。

Surface-localized glycoproteins act through class C ARFs to fine-tune gametophore initiation in Physcomitrium patens.

机构信息

Institute of Plant and Microbial Biology, Academia Sinica, 128 Sec.2, Academia Rd., Nankang, Taipei 11529, Taiwan.

Department of Biological Sciences, Faculty of Science, Hokkaido University, Kita 10 Nishi 8, Kita-ku, Sapporo 060-0810, Japan.

出版信息

Development. 2022 Dec 15;149(24). doi: 10.1242/dev.200370.

Abstract

Arabinogalactan proteins are functionally diverse cell wall structural glycoproteins that have been implicated in cell wall remodeling, although the mechanistic actions remain elusive. Here, we identify and characterize two AGP glycoproteins, SLEEPING BEAUTY (SB) and SB-like (SBL), that negatively regulate the gametophore bud initiation in Physcomitrium patens by dampening cell wall loosening/softening. Disruption of SB and SBL led to accelerated gametophore formation and altered cell wall compositions. The function of SB is glycosylation dependent and genetically connected with the class C auxin response factor (ARF) transcription factors PpARFC1B and PpARFC2. Transcriptomics profiling showed that SB upregulates PpARFC2, which in turn suppresses a range of cell wall-modifying genes that are required for cell wall loosening/softening. We further show that PpARFC2 binds directly to multiple AuxRE motifs on the cis-regulatory sequences of PECTIN METHYLESTERASE to suppress its expression. Hence, our results demonstrate a mechanism by which the SB modulates the strength of intracellular auxin signaling output, which is necessary to fine-tune the timing of gametophore initials formation.

摘要

阿拉伯半乳聚糖蛋白是功能多样的细胞壁结构糖蛋白,它们被认为参与细胞壁重塑,尽管其作用机制仍不清楚。在这里,我们鉴定和表征了两个 AGP 糖蛋白,即 SLEEPING BEAUTY(SB)和 SB-like(SBL),它们通过抑制细胞壁松弛/软化来负调控Physcomitrium patens 中的配子体芽起始。SB 和 SBL 的破坏导致配子体形成加速和细胞壁成分改变。SB 的功能依赖于糖基化,并且与 C 类生长素响应因子(ARF)转录因子 PpARFC1B 和 PpARFC2 具有遗传联系。转录组学分析显示,SB 上调 PpARFC2,而 PpARFC2 又抑制一系列细胞壁修饰基因的表达,这些基因对于细胞壁松弛/软化是必需的。我们进一步表明,PpARFC2 直接结合到多聚半乳糖醛酸甲酯酶顺式调控序列上的多个 AuxRE 基序,从而抑制其表达。因此,我们的结果表明,SB 调节细胞内生长素信号输出强度的机制,这对于微调配子体起始的时间是必要的。

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