Sökning: onr:"swepub:oai:DiVA.org:uu-214442" >
Novel disease-causi...
Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure
-
van Kuilenburg, André B P (författare)
-
- Dobritzsch, Doreen, 1972- (författare)
- Karolinska Institutet
-
Meinsma, Rutger (författare)
-
visa fler...
-
Haasjes, Janet (författare)
-
Waterham, Hans R (författare)
-
Nowaczyk, Malgorzata J M (författare)
-
Maropoulos, George D (författare)
-
Hein, Guido (författare)
-
Kalhoff, Hermann (författare)
-
Kirk, Jean M (författare)
-
Baaske, Holger (författare)
-
Aukett, Anne (författare)
-
Duley, John A (författare)
-
Ward, Kate P (författare)
-
- Lindqvist, Ylva (författare)
- Karolinska Institutet
-
van Gennip, Albert H (författare)
-
visa färre...
-
(creator_code:org_t)
- Portland Press Ltd. 2002
- 2002
- Engelska.
-
Ingår i: Biochemical Journal. - : Portland Press Ltd.. - 0264-6021 .- 1470-8728. ; 364:Pt 1, s. 157-163
- Relaterad länk:
-
https://europepmc.or...
-
visa fler...
-
https://urn.kb.se/re...
-
http://kipublication...
-
https://doi.org/10.1...
-
visa färre...
Abstract
Ämnesord
Stäng
- Dihydropyrimidine dehydrogenase (DPD) deficiency is an autosomal recessive disease characterized by thymine-uraciluria in homozygous deficient patients. Cancer patients with a partial deficiency of DPD are at risk of developing severe life-threatening toxicities after the administration of 5-fluorouracil. Thus, identification of novel disease-causing mutations is of the utmost importance to allow screening of patients at risk. In eight patients presenting with a complete DPD deficiency, a considerable variation in the clinical presentation was noted. Whereas motor retardation was observed in all patients, no patients presented with convulsive disorders. In this group of patients, nine novel mutations were identified including one deletion of two nucleotides [1039-1042delTG] and eight missense mutations. Analysis of the crystal structure of pig DPD suggested that five out of eight amino acid exchanges present in these patients with a complete DPD deficiency, Pro86Leu, Ser201Arg, Ser492Leu, Asp949Val and His978Arg, interfered directly or indirectly with cofactor binding or electron transport. Furthermore, the mutations Ile560Ser and Tyr211Cys most likely affected the structural integrity of the DPD protein. Only the effect of the Ile370Val and a previously identified Cys29Arg mutation could not be readily explained by analysis of the three-dimensional structure of the DPD enzyme, suggesting that at least the latter might be a common polymorphism. Our data demonstrate for the first time the possible consequences of missense mutations in the DPD gene on the function and stability of the DPD enzyme.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
Hitta via bibliotek
Till lärosätets databas
- Av författaren/redakt...
-
van Kuilenburg, ...
-
Dobritzsch, Dore ...
-
Meinsma, Rutger
-
Haasjes, Janet
-
Waterham, Hans R
-
Nowaczyk, Malgor ...
-
visa fler...
-
Maropoulos, Geor ...
-
Hein, Guido
-
Kalhoff, Hermann
-
Kirk, Jean M
-
Baaske, Holger
-
Aukett, Anne
-
Duley, John A
-
Ward, Kate P
-
Lindqvist, Ylva
-
van Gennip, Albe ...
-
visa färre...
- Om ämnet
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Medicinska och f ...
-
och Medicinsk geneti ...
- Artiklar i publikationen
-
Biochemical Jour ...
- Av lärosätet
-
Uppsala universitet
-
Karolinska Institutet