Tulin Lab

Overview of Research Interests

Chromatin Programming and Transcription

PARP=1 protein localization in salivary gland

Developmentally regulated gene expression in multicellular eukaryotes requires the formation of dynamic tissue-specific chromatin structures that participate in activating certain genes and silencing others (Wolffe, Essays Biochem. 37:45, 2001). Furthermore, during an organism’s lifetime the established pattern of chromatin needs to be quickly reprogrammed in a response to environmental or hormonal signals (Thummel, Insect Biochem. Mol. Biol. 32:113, 2002). It has become increasingly clear that key aspects of chromatin structure and gene transcriptional activity are determined by a specific modification of histones (Elgin and Workman, Curr Opin Genet Dev. 12: 127, 2002; Fischle et al., Nature. 425:475, 2003).


Despite this exciting progress there remains much to be learned  about how chromatin is programmed and how active or inactive domains are maintained. Our studies of the abundant nuclear  enzyme poly(ADP-ribose) polymerase (PARP) and poly(ADP-  ribose) glycohydrolase (PARG) demonstrated that it plays novel  and previously unknown roles in many of these processes.  Distributed evenly along chromatin PARP is responsible for rapid local chromatin decondensation (loosening), which  is required for transcriptional activation of many genes within particular chromatin blocks. Previously we have  demonstrated that poly(ADP-ribosyl)ation is also involved in heterochromatin formation, the initiation and  maintenance of nucleoli and telomere metabolism. The presence of several PARP-related proteins in mammals  complicates the analysis and interpretation of results. Fortunately, only a single PARP gene is present in the Drosophila genome, making this animal an invaluable model system to study  PARP function. Using Drosophila we study the molecular mechanisms of PARP activation, its action on chromatin and the interaction of PARP with other components of the chromatin remodeling machinery and transcriptional apparatus.