Published in:
01-02-2013 | Clinical Study
A c.464T>A mutation in VHL gene in a Chinese family with VHL syndrome
Authors:
Yan Lu, Jun Lu, Qiang Liu, Jian Niu, Shi-Ming Zhang, Qing-Yu Wu, Xiao-Fei Qi
Published in:
Journal of Neuro-Oncology
|
Issue 3/2013
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Abstract
Von Hippel–Lindau (VHL) is a tumor suppressor that negatively regulates the production of angiogenic factors. Mutations in the VHL gene cause VHL syndrome, which is characterized by highly vascularized tumors. Here we report a c.464T>A mutation of the VHL gene in three patients with hemangioblastoma from a Chinese family. This mutation was not reported previously and was absent in the unaffected family members. The mutation is predicted to cause Val to Glu substitution at VHL protein residue 155 in a conserved region. Previous biochemical studies demonstrated that residue Val-155 was critical for VHL protein binding to chaperonin TRiC/CCT, an essential step for proper VHL protein folding. Our finding of naturally occurring VHL V155E mutation in patients with VHL syndrome supports the functional importance of Val-155 residue in VHL protein and illustrates the diversity of VHL gene defects underlying VHL syndrome.