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Sökning: WFRF:(Nilsson Torbjörn 1956 ) > A folate receptor a...

A folate receptor alpha double-mutated haplotype 1816delC-1841A is distributed throughout Eurasia and associated with lower erythrocyte folate levels

Nilsson, Torbjörn K., 1956- (författare)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Department of Laboratory Medicine, Clinical Chemistry, Örebro University Hospital, Örebro, Sweden,Department of Laboratory Medicine, Clinical Chemistry, Örebro University Hospital, and School of Health and Medical Sciences, Örebro University
Laanpere, Margit (författare)
Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia
Altmae, Signe (författare)
Department of Clinical Science, Intervention and Technology, Division of Obstetrics and Gynaecology, Karolinska University Hospital Huddinge, Karolinska Institute, Stockholm, Sweden; Competence Centre On Reproductive Medicine and Biology, Tartu, Estonia
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Serra-Majem, Lluis (författare)
Department of Clinical Sciences, School of Health Sciences, University of Las Palmas of Gran Canaria, Las Palmas, Spain
Salumets, Andres (författare)
Competence Centre On Reproductive Medicine and Biology, Tartu, Estonia
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 (creator_code:org_t)
2011-09-22
2012
Engelska.
Ingår i: Molecular Biology Reports. - Dordrecht, Netherlands : Springer. - 0301-4851 .- 1573-4978. ; 39:4, s. 4471-4478
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Folate is crucial for various cellular functions. Several transport mechanisms allow folate to enter the intracellular compartment with folate receptor-alpha being the major high-affinity receptor. Rare genetic variations in exons of the FR-alpha gene, FOLR1, were recently shown to cause severe folate deficiency accompanied by neurological and other disturbances. So far, similar effects by genetic variation in noncoding parts of the FOLR1 gene have not been identified. The aim of our study was to determine biochemically the haplotype structure of two linked polymorphisms in the FOLR1 gene, 1816delC and 1841G > A, the prevalences of the mutated alleles across Eurasia, and their possible effects on physiological folate levels in vivo. For this purpose we employed allele-specific PCR and Pyrosequencing technology and performed genotyping in 738 subjects from Spain, 387 from Sweden, 952 from Estonia, and 47 from Korea. We demonstrate the presence of an ancient double-mutated haplotype 1816delC-1841A in the FOLR1 gene, with the prevalence of the mutated allele being highest among Koreans (q = 0.074), lower in Estonians (q = 0.017), Spaniards (q = 0.0061), and the lowest among Swedes (q = 0.0026). Erythrocyte folate levels were studied in the Spanish population sample, where subjects carrying the double-mutated FOLR1 haplotype had significantly reduced levels by 27% (P = 0.039), adjusted for serum vitamin B-12 levels and MTHFR 677C > T genotype, while the mean serum folate levels were only 20% lower among the carriers (P = 0.11). Plasma homocysteine and cobalamin levels did not differ. Thus, we have demonstrated by molecular haplotyping an ancient double-mutated haplotype 1816delC-1841A in the FOLR1 gene, spread over the whole Eurasian continent, which may be of functional importance for uptake of folate in red blood cells.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Nyckelord

Folate receptor
FOLR1
Haplotype
Homocysteine
Polymorphism
Biomedicin
Biomedicine

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