Convergent evolution of water conducting cells in Marchantia recruited the ZHOUPI gene promoting cell wall reinforcement and programmed cell death

A key adaptation of plants to life on land is the formation of water conducting cells (WCC) for efficient long-distance water transport. Based on morphological analyses it is thought that WCC have evolved independently on multiple occasions. For example, WCC have been lost in all but a few lineages of bryophytes but strikingly, within the liverworts a derived group, the complex thalloids, has evolved a novel externalised water conducting tissue composed of reinforced, hollow cells termed pegged rhizoids. Here we show that pegged rhizoid differentiation in Marchantia polymorpha is controlled by orthologues of the ZHOUPI and ICE bHLH transcription factors required for endosperm cell death in Arabidopsis seeds. By contrast, pegged rhizoid development was not affected by disruption of MpNAC5, the Marchantia orthologue of the VND genes that control WCC formation in flowering plants. We characterize the rapid, genetically controlled programmed cell death process that pegged rhizoids undergo to terminate cellular differentiation, and identify a corresponding upregulation of conserved putative plant cell death effector genes. Lastly, we show that ectopic expression of MpZOU1 increases production of pegged rhizoids and enhances drought tolerance. Our results support that pegged rhizoids having evolved independently of other WCC. We suggest that elements of the genetic control of developmental cell death are conserved throughout land plants and that the ZHOUPI/ICE regulatory module has been independently recruited to promote cell wall modification and programmed cell death in liverwort rhizoids and in the endosperm of flowering plant seed