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NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24

Hunter, M., Angelicheva, D., Tournev, I., Ingley, E.ORCID: 0000-0002-8112-9134, Chan, D.C., Watts, G.F., Kremensky, I. and Kalaydjieva, L. (2005) NDRG1 interacts with APO A-I and A-II and is a functional candidate for the HDL-C QTL on 8q24. Biochemical and Biophysical Research Communications, 332 (4). pp. 982-992.

Link to Published Version: https://doi.org/10.1016/j.bbrc.2005.05.050
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Abstract

Hereditary Motor and Sensory Neuropathy Lom (HMSNL) is a severe autosomal recessive peripheral neuropathy, the most common form of demyelinating Charcot-Marie-Tooth (CMT) disease in the Roma (Gypsy) population. The mutated gene, N-myc downstream-regulated gene 1 (NDRG1), is widely expressed and has been implicated in a range of processes and pathways. To gain an insight into NDRG1 function we performed yeast two-hybrid screening and identified interacting proteins whose known functions suggest involvement in cellular trafficking. Further analyses, focusing on apolipoproteins A-I and A-II, confirmed their interaction with NDRG1 in mammalian cells and suggest a defect in Schwann cell lipid trafficking as a major pathogenetic mechanism in HMSNL. At the same time, the chromosomal location of NDRG1 coincides with a reported HDL-C QTL in humans and in mice. A putative role of NDRG1 in the general mechanisms of HDL-mediated cholesterol transport was supported by biochemical studies of blood lipids, which revealed an association between the Gypsy founder mutation, R148X, and decreased HDL-C levels.

Item Type: Journal Article
Publisher: Academic Press
Copyright: © 2005 Elsevier Inc.
URI: http://researchrepository.murdoch.edu.au/id/eprint/39565
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