Hermann Steller, Ph.D.


Hermann Steller, Ph.D.


We are using a multidisciplinary approach that integrates Drosophila genetics and molecular biology with mammalian cell culture experiments and biochemical and structural studies. From surveying a large fraction of the Drosophila genome for genes that are required for programmed cell, three apoptotic activators, termed reaper, head involution defective (hid), and grim were identified. All three genes are necessary and sufficient for the activation of apoptosis in Drosophila. Significantly, reaper, hid and grim are all transcriptionally regulated by a variety of death-inducing stimuli, including steroid hormones, segmentation and patterning genes, and DNA damaging agents. Therefore, it appears that these genes act as integrators for relaying different apoptotic signals to the core death program . In order to gain further insight into the mechanism by which reaper hid and grim induce apoptosis, we have designed very sensitive and powerful genetic screens to identify additional cell death genes in Drosophila. These studies have revealed that the cell-killing activity of the HID protein is inactivated upon phosphorylation by MAPK, and this provides an explanation for how survival signals acting through the Ras/MAPK pathway can suppress the induction of apoptosis. We have also isolated and characterized mutations in the Drosophila inhibitor of apoptosis protein-1(diap1) gene, and this work demonstrated that Reaper, Hid and Grim kill by inhibiting the anti-apoptotic activity of Diap1. We recently found that Reaper, but not Hid, promotes auto-ubiquitination and self-destruction of Diap1. These results suggest a novel strategy for the selective elimination of tumor cells that express elevated IAP protein levels.

We have also characterized a Drosophila homolog of ced-4/Apaf-1, termed hac-1 (for homolog of Apaf-1 and ced-4). Hac-1 is structurally and functionally very similar to Apaf-1 and is required for normal cell death during embryonic development in Drosophila. Our results demonstrate that death-inducing stimuli can simultaneously activate two distinct regulatory pathways controlling caspase activation in Drosophila. We believe that such a dual regulatory input on caspase activation operates also during the control of apoptosis in mammalian cells.

Certain cells, including terminally differentiated neurons in Drosophila, are highly resistant towards cell death. By using Drosophila photoreceptor development as a model system, we hope to gain insights into the survival mechanisms employed for resistance to apoptosis (see more detailed research projects). Since the mechanism of apoptosis has been conserved in evolution from worms to insects to man, knowledge gained from studying cell death in Drosophila is likely to apply to mammalian systems as well. In order to test this directly, we are studying the activity of Drosophila cell death genes and their mouse or human homologues in cultured mammalian cells. We are also interested in biochemical and structural studies of selected cell death proteins in order to determine their precise mechanism of action. We expect that knowledge gained from this work can ultimately be exploited to manipulate apoptosis for therapeutic benefits

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