Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency

• Published in: Human molecular genetics 2003-06, Vol.12 (11), p.1241-1252
• Main Authors: Alam, N.A., Rowan, A.J., Wortham, N.C., Pollard, P.J., Mitchell, M., Tyrer, J.P., Barclay, E., Calonje, E., Manek, S., Adams, S.J., Bowers, P.W., Burrows, N.P., Charles-Holmes, R., Cook, L.J., Daly, B.M., Ford, G.P., Fuller, L.C., Hadfield-Jones, S.E., Hardwick, N., Highet, A.S., Keefe, M., MacDonald-Hull, S.P., Potts, E.D.A., Crone, M., Wilkinson, S., Camacho-Martinez, F., Jablonska, S., Ratnavel, R., MacDonald, A., Mann, R.J., Grice, K., Guillet, G., Lewis-Jones, M.S., McGrath, H., Seukeran, D.C., Morrison, P.J., Fleming, S., Rahman, S., Kelsell, D., Leigh, I., Olpin, S., Tomlinson, I.P.M.
• Format: Article
• Language: English
• Subjects: Amino Acid Metabolism, Inborn Errors - genetics; Amino Acid Sequence; Biological and medical sciences; Enzyme Stability; Female; Fumarate Hydratase - chemistry; Fumarate Hydratase - deficiency; Fumarate Hydratase - genetics; Fumarate Hydratase - metabolism; Genetic Predisposition to Disease; Germ-Line Mutation; Gynecology. Andrology. Obstetrics; Humans; Kidney Neoplasms - genetics; Kidney Neoplasms - secondary; Leiomyomatosis - genetics; Leiomyomatosis - pathology; Mammary gland diseases; Medical sciences; Molecular Sequence Data; Mutation; Protein Conformation; RNA Stability; RNA, Messenger - metabolism; Sequence Homology, Amino Acid; Skin Neoplasms - genetics; Skin Neoplasms - pathology; Tumors; Uterine Neoplasms - genetics; Uterine Neoplasms - pathology
• ISSN: 0964-6906; 1460-2083; 1460-2083
• DOI: 10.1093/hmg/ddg148

Germline mutations of the fumarate hydratase (FH, fumarase) gene are found in the recessive FH deficiency syndrome and in dominantly inherited susceptibility to multiple cutaneous and uterine leiomyomatosis (MCUL). We have previously reported a number of germline FH mutations from MCUL patients. In this study, we report additional FH mutations in MCUL and FH deficiency patients. Mutations can readily be found in about 75% of MCUL cases and most cases of FH deficiency. Some of the more common FH mutations are probably derived from founding individuals. Protein-truncating FH mutations are functionally null alleles. Disease-associated missense FH changes map to highly conserved residues, mostly in or around the enzyme's active site or activation site; we predict that these mutations severely compromise enzyme function. The mutation spectra in FH deficiency and MCUL are similar, although in the latter mutations tend to occur earlier in the gene and, perhaps, are more likely to result in a truncated or absent protein. We have found that not all mutation-carrier parents of FH deficiency children have a strong predisposition to leiomyomata. We have confirmed that renal carcinoma is sometimes part of MCUL, as part of the variant hereditary leiomyomatosis and renal cancer (HLRCC) syndrome, and have shown that these cancers may have either type II papillary or collecting duct morphology. We have found no association between the type or site of FH mutation and any aspect of the MCUL phenotype. Biochemical assay for reduced FH functional activity in the germline of MCUL patients can indicate carriers of FH mutations with high sensitivity and specificity, and can detect reduced FH activity in some patients without detectable FH mutations. We conclude that MCUL is probably a genetically homogeneous tumour predisposition syndrome, primarily resulting from absent or severely reduced fumarase activity, with currently unknown functional consequences for the smooth muscle or kidney cell.