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Masle, J.

Publications and source records attributed to Masle, J..

2 recordsLinked to original sources

Timing seed germination under changing salinity: a key role of the ERECTA receptor-kinases

Appropriate timing of seed germination is crucial for the survival and propagation of plants, and for crop yield, especially in environments prone to salinity or drought. Yet, how exactly seeds perceive changes in soil conditions and integrate them to trigger germination remains elusive, especially once non-dormant. Here we report that the Arabidopsis ERECTA (ER), ERECTA-LIKE1 (ERL1) and ERECTA-LIKE2 (ERL2) leucine-rich-repeat receptor-like kinases synergistically regulate germination and its sensitivity to salinity and osmotic stress. Loss of ER alone, or in combination with ERL1 and/or ERL2 slows down the initiation of germination and its progression to completion, or arrests it altogether until better conditions return. That function is maternally controlled via the embryo surrounding tissues, primarily the properties of the seed coat determined during seed development on the mother plant, that relate to both seed coat expansion and subsequent differentiation, particularly the formation of its mucilage. Salt-hypersensitive er, er erl1, er erl2 and triple mutant seeds also exhibit increased sensitivity to ABA during germination, and under salinity show an enhanced upregulation of the germination repressors and inducers of dormancy ABA-insensitive-3, ABA-insensitive-5, DELLA encoding RGL2 and Delay-Of-Germination-1. These findings reveal a novel role of the ERECTA kinases in the sensing of conditions at the seed surface and the integration of developmental and stress signalling pathways in seeds. They also open novel avenues for the genetic improvement of plant adaptation to harsh soils.\n\nHighlightThe ERECTA family of receptor-kinases regulates seed germination under salinity, through mucilage-mediated sensing of conditions at the seed surface, and interaction with secondary dormancy mechanisms.

plant biology

Systemic signalling through TCTP1 controls lateral root formation in Arabidopsis

As in animals, the plant body plan and primary organs are established during embryogenesis. However, plants have the ability to generate new organs and functional units throughout their whole life. These are produced through the specification, initiation and differentiation of secondary meristems, governed by the intrinsic genetic program and cues from the environment. They give plants an extraordinary developmental plasticity to modulate their size and architecture according to environmental constraints and opportunities. How this plasticity is regulated at the whole organism level is still largely elusive. In particular the mechanisms regulating the iterative formation of lateral roots along the primary root remain little known. A pivotal role of auxin is well established and recently the role of local mechanical signals and oscillations in transcriptional activity has emerged. Here we provide evidence for a role of Translationally Controlled Tumor Protein (TCTP), a vital ubiquitous protein in eukaryotes. We show that Arabidopsis AtTCTP1 controls root system architecture through a dual function: as a general constitutive growth promoter locally, and as a systemic signalling agent via mobility from the shoot. Our data indicate that this signalling function is specifically targeted to the pericycle and modulates the frequency of lateral root initiation and emergence sites along the primary root, and the compromise between branching and elongating, independent of shoot size. Plant TCTP genes show high similarity among species. TCTP messengers and proteins have been detected in the vasculature of diverse species. This suggests that the mobility and extracellular signalling function of AtTCTP1 to control root organogenesis might be widely conserved within the plant kingdom, and highly relevant to a better understanding of post-embryonic formation of lateral organs in plants, and the elusive coordination of shoot and root morphogenesis.

plant biology