Programmed cell death (PCD) is an essential process in the development of animals and plants that is under tight regulatory control. Uncontrolled PCD can lead to disease and death, therefore organisms need sophisticated mechanisms to ensure PCD occurs in a controlled manner. In contrast to forms of animal PCD such as apoptosis, surprisingly little is known about the developmentally controlled PCD (dPCD) in plants. Recent findings that dPCD occurs in the root cap of the plant Arabidopsis offer a unique opportunity to study dPCD in the development of an easily accessible plant organ. The root cap surrounds the growing root tip and has a tightly regulated organ size. This organ size uniformity is achieved by a precise balance between cell division and dPCD. Using the root cap as a dPCD model, I aim to contribute to the understanding of this essential process in plants. To do so, I will use an innovative genetic screen to unravel the role of cellular communication in dPCD. Targeted genome editing by CRISPR/Cas will be used to generate
combinations of mutant plants, allowing me to overcome the functional redundancy in the large gene family of plant receptors. In parallel, I will employ a classical mutant screen to identify novel components of dPCD in an unbiased fashion. Finally, I will perform an in-depth functional analysis
of genes identified by these two approaches to unravel their role in the complex communication system plants use to coordinate dPCD.