HIP12 is a non-proapoptotic member of a gene family including HIP1, an interacting protein with huntingtin

Springer Science and Business Media LLC - Tập 11 - Trang 1006-1015 - 2000
Vikramjit S. Chopra1, Martina Metzler1, Dita M. Rasper2, Asa E.Y. Engqvist-Goldstein3, Roshni Singaraja1, Lu Gan1, Keith M. Fichter1, Krista McCutcheon1, David Drubin3, Donald W. Nicholson2, Michael R. Hayden1
1Department of Medical Genetics, and Centre for Molecular Medicine and Therapeutics, University of British Columbia, 980 West 28th Avenue, Vancouver, British Columbia, V5Z 4H4, Canada, , CA
2Department of Biochemistry and Molecular Biology, Merck Frosst Centre for Therapeutic Research, Montreal, Quebec, Canada, , CA
3Department of Molecular and Cell Biology, University of California, Berkeley, California, USA, , US

Tóm tắt

Huntingtin-interacting protein 1 (HIP1) is a membrane-associated protein that interacts with huntingtin, the protein altered in Huntington disease. HIP1 shows homology to Sla2p, a protein essential for the assembly and function of the cytoskeleton and endocytosis in Saccharomyces cerevisiae. We have determined that the HIP1 gene comprises 32 exons spanning approximately 215 kb of genomic DNA and gives rise to two alternate splice forms termed HIP1-1 and HIP1-2. Additionally, we have identified a novel protein termed HIP12 with significant sequence and biochemical similarities to HIP1 and high sequence similarity to Sla2p. HIP12 differs from HIP1 in its pattern of expression both at the mRNA and protein level. However, HIP1 and HIP12 are both found within the brain and show a similar subcellular distribution pattern. In contrast to HIP1, which is toxic in cell culture, HIP12 does not confer toxicity in the same assay systems. Interestingly, HIP12 does not interact with huntingtin but can interact with HIP1, suggesting a potential interaction in vivo that may influence the function of each respective protein.