Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

The von Hippel-Lindau (VHL) tumor suppressor functions as a ubiquitin ligase that mediates proteolytic inactivation of hydroxylated alpha subunits of hypoxia-inducible factor (HIF). Although studies of VHL-defective renal carcinoma cells suggest the existence of other VHL tumor suppressor pathways, dysregulation of the HIF transcriptional cascade has extensive effects that make it difficult to distinguish whether, and to what extent, observed abnormalities in these cells represent effects on pathways that are distinct from HIF. Here, we report on a genetic analysis of HIF-dependent and -independent effects of VHL inactivation by studying gene expression patterns in Caenorhabditis elegans. We show tight conservation of the HIF-1/VHL-1/EGL-9 hydroxylase pathway. However, persisting differential gene expression in hif-1 versus hif-1; vhl-1 double mutant worms clearly distinguished HIF-1-independent effects of VHL-1 inactivation. Genomic clustering, predicted functional similarities, and a common pattern of dysregulation in both vhl-1 worms and a set of mutants (dpy-18, let-268, gon-1, mig-17, and unc-6), with different defects in extracellular matrix formation, suggest that dysregulation of these genes reflects a discrete HIF-1-independent function of VHL-1 that is connected with extracellular matrix function.

Original publication

DOI

10.1371/journal.pbio.0020289

Type

Journal article

Journal

PLoS Biol

Publication Date

10/2004

Volume

2

Keywords

Animals, Base Sequence, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Chromosome Mapping, Cluster Analysis, Computational Biology, Down-Regulation, Evolution, Molecular, Extracellular Matrix, Gene Expression Regulation, Genome, Humans, Models, Genetic, Molecular Sequence Data, Mutation, Oligonucleotide Array Sequence Analysis, Ribonucleases, Time Factors, Up-Regulation, Von Hippel-Lindau Tumor Suppressor Protein