Literature DB >> 28836669

Vacuolar processing enzyme 4 contributes to maternal control of grain size in barley by executing programmed cell death in the pericarp.

Volodymyr Radchuk1, Van Tran1, Ruslana Radchuk1, Mercedes Diaz-Mendoza2, Diana Weier1, Joerg Fuchs1, David Riewe1, Goetz Hensel1, Jochen Kumlehn1, Eberhard Munz1, Nicolas Heinzel1, Hardy Rolletschek1, Manuel Martinez2, Ljudmilla Borisjuk1.   

Abstract

The angiosperm embryo and endosperm are limited in space because they grow inside maternal seed tissues. The elimination of cell layers of the maternal seed coat by programmed cell death (PCD) could provide space and nutrition to the filial organs. Using the barley (Hordeum vulgare L.) seed as a model, we elucidated the role of vacuolar processing enzyme 4 (VPE4) in cereals by using an RNAi approach and targeting the enzymatic properties of the recombinant protein. A comparative characterization of transgenic versus wild-type plants included transcriptional and metabolic profiling, flow cytometry, histology and nuclear magnetic imaging of grains. The recombinant VPE4 protein exhibited legumain and caspase-1 properties in vitro. Pericarp disintegration was delayed in the transgenic grains. Although the VPE4 gene and enzymatic activity was decreased in the early developing pericarp, storage capacity and the size of the endosperm and embryo were reduced in the mature VPE4-repressed grains. The persistence of the pericarp in the VPE4-affected grains constrains endosperm and embryo growth and leads to transcriptional reprogramming, perturbations in signalling and adjustments in metabolism. We conclude that VPE4 expression executes PCD in the pericarp, which is required for later endosperm filling, and argue for a role of PCD in maternal control of seed size in cereals.
© 2017 The Authors. New Phytologist © 2017 New Phytologist Trust.

Entities:  

Keywords:  barley; caspase-like activities; grain size; maternal control of seed size; pericarp; programmed cell death (PCD); vacuolar processing enzyme

Mesh:

Substances:

Year:  2017        PMID: 28836669     DOI: 10.1111/nph.14729

Source DB:  PubMed          Journal:  New Phytol        ISSN: 0028-646X            Impact factor:   10.151


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