The nucleus is arguably one of the most important organelles in the cell, and yet surprisingly little is known about how its shape is maintained and what determines its size. The importance of nuclear shape is underscored by the fact that various diseases, including cancer and premature aging, are associated with changes in nuclear shape, and yet the relationship between nuclear shape and nuclear function is poorly understood. In most metazoan cells, the nuclear envelope (NE) undergoes cycles of assembly and disassembly in each and every cell cycle, and one of the key outstanding questions in the field is which proteins facilitate these processes. To gain insight into NE dynamics, we initiated the C. elegans nuclear architecture project. This project has two main components: (a) to examine in C. elegans the role of proteins identified in a yeast screen as being involved in nuclear architecture (project DK057807); and (b) to screen for additional gene/proteins involved in determining nuclear shape and size, and in affecting NE breakdown and reassembly. In the past year we focused on the second goal, while the first goal awaits the discovery of additional yeast genes involved in nuclear morphology. Following our observation in budding yeast that Cdc5, the yeast homolog of polo kinase, affects nuclear morphology, we are also examining the role of the C. elegans polo kinase, PLK-1, in NE dynamics. We discovered that PLK-1 is required for nuclear envelope breakdown during early embryogenesis. In particular, PLK-1 is essential for breaching the NEs that separate the maternal and paternal chromosomes. Following fertilization in C. elegans, the maternal and paternal chromosomes become encased in NEs. These pronuclei migrate towards each other and become juxtaposed such that between there two pronuclei there are 4 closely apposed membranes (2 from each NE). During mitosis, the NE disassembles and the nuclear membrane retreats into the rest of the ER. The dissamebly of the NEs between the two pronuclei involves the formation of a membrane gap that spans all 4 membranes. The gap is critical for the mixing of the parental genomes. We found that when PLK-1 is down regulated, the gap does not form and the maternal and paternal genomes remain segregated in two separate nuclei in all subsequent embryonic divisions. How PLK-1 induces gap formation and what is the mechanism by which this gap is formed in currently under investigation. We also generated a photo-switchable tagged histone H2B and used it to follow germline lineage in C. elegans. This tool allowed us to determine where and when cells divide and to establish, for the first time in live worms, which population of cells serves as germ cells.
