Search for: All records

The shoot of green plants is the primary site of carbon assimilation into sugars, the key source of energy and metabolic building blocks. The systemic transport of sugars is essential for plant growth and morphogenesis. Plants evolved intricate networks of molecular players to effectively orchestrate the subcellular partitioning of sugars. Dynamic distribution of these osmotically active compounds is a handy tool to regulate cell turgor pressure. Pressure-induced mechanical forces play an instructive role in developmental biology across kingdoms. Here, we functionally characterized a long non-coding RNA,CARMA,as a negative regulator of a receptor-like kinase, CANAR. Sugar-responsiveCARMAspecifically fine-tunesCANARexpression in the phloem, the route of sugar transport. By controlling sugar distribution, the CARMA-CANAR module allows cells to flexibly adapt to the external osmolality and adjust the size of vascular cell types during organ growth and development. We identify a nexus of plant vascular tissue formation with cell internal pressure monitoring and reveal a novel functional aspect of long non-coding RNAs in developmental biology.

 

Cell division is often regulated by extracellular signaling networks to ensure correct patterning during development. In Arabidopsis , the SHORT-ROOT (SHR)/SCARECROW (SCR) transcription factor dimer activates CYCLIND6 ; 1 ( CYCD6;1 ) to drive formative divisions during root ground tissue development. Here, we show plasma-membrane-localized BARELY ANY MERISTEM1/2 (BAM1/2) family receptor kinases are required for SHR -dependent formative divisions and CYCD6;1 expression, but not SHR -dependent ground tissue specification. Root-enriched CLE ligands bind the BAM1 extracellular domain and are necessary and sufficient to activate SHR -mediated divisions and CYCD6;1 expression. Correspondingly, BAM-CLE signaling contributes to the restriction of formative divisions to the distal root region. Additionally, genetic analysis reveals that BAM-CLE and SHR converge to regulate additional cell divisions outside of the ground tissues. Our work identifies an extracellular signaling pathway regulating formative root divisions and provides a framework to explore this pathway in patterning and evolution.