Autophagy and metacaspase determine the mode of cell death in plants

Although animals eliminate apoptotic cells using macrophages, plants use cell corpses throughout development and disassemble cells in a cell-autonomous manner by vacuolar cell death. During vacuolar cell death, lytic vacuoles gradually engulf and digest the cytoplasmic content. On the other hand, acute stress triggers an alternative cell death, necrosis, which is characterized by mitochondrial dysfunction, early rupture of the plasma membrane, and disordered cell disassembly. How both types of cell death are regulated remains obscure. In this paper, we show that vacuolar death in the embryo suspensor of Norway spruce requires autophagy. In turn, activation of autophagy lies downstream of metacaspase mcII-Pa, a key protease essential for suspensor cell death. Genetic suppression of the metacaspase–autophagy pathway induced a switch from vacuolar to necrotic death, resulting in failure of suspensor differentiation and embryonic arrest. Our results establish metacaspase-dependent autophagy as a bona fide mechanism that is responsible for cell disassembly during vacuolar cell death and for inhibition of necrosis.

Sexual reproduction in grand fir (Abies grandis)

Phenology and anatomy of the postdormancy reproductive phase of Abies grandis Lindl, were studied. The dormant microsporangia contained compactly arranged pollen mother cells (PMC). The pollen cones broke dormancy in the 3rd week of February and soon afterwards the PMC entered meiosis. Microspore tetrads formed by the 2nd week of March. Pollen grains were shed at the five-celled stage in the 3rd week of April. The pollen grains were bisaccate and showed a triradiate mark on the proximal pole. The dormant ovulate-cone buds bore rudimentary ovuliferous scales, each with two ovular areas. Ovulate cones broke dormancy at the end of January. Megaspore mother cells differentiated by the end of February and the integument was initiated soon afterwards. A megaspore triad formed in the 2nd week of April. By the 3rd week of April, at the time of pollination, the ovule contained a free-nuclear gametophyte, and the integument had developed a stigmatic micropylar funnel. Numerous microdroplets were observed on the surface of the funnel to which pollen adhered. After pollination the funnel became infolded, enclosing the pollen grains. Pollen germination, pollen tube growth through the nucellus, and syngamy took only 3–4 days and occurred in the 3rd week of June. The female gametophyte was long and bore two or three archegonia. The proembryo consisted of four tiers of four cells each. The suspensors developed from the subterminal tier of cells. The four terminal cells formed the embryonal mass, whose proximal cells elongated and developed into a secondary suspensor. Differentiation of the root apical meristem and the cotyledons in the young embryo occurred in the 1st week of July and the embryo matured in the 3rd week of August.