DNA sequence · 1997 · 18 citations · 16 references
Life SciencesGeneticsMolecular GeneticsGenomicsHuman GeneticsMedical GeneticsGenetic DisordersGenome SequencingGenomic VariationVariant DetectionIntron OrganizationPolymorphic TypesPyruvate Kinase DeficiencySingle Origin Hypothesis
The human pyruvate kinase L/R-gene has been completely sequenced in unrelated normal individuals and in pyruvate kinase-deficient patients by a PCR-based direct genomic sequencing approach and analyzed for polymorphisms. The total length of the gene is 8409 nucleotides. Four polymorphic sites have been detected: C/A1705 and C/T1992 in exon 12, a T-stretch in intron 1 occurring in the two polymorphic forms (T)10 and (T)19 and an (ATT)n microsatellite in intron J which has been found in the variation (ATT)11-17. Haplotype analysis using these four markers has been applied to trace the genetic background in PK-deficiencies. The results support the idea of a single origin of most of the individual PK-mutations.
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The origin of the major cystic fibrosis mutation (ΔF508) in European populations
Núria Morral, Jaume Bertranpetit, Xavier Estivill et al. · Nature Genetics · 1994 · 347 citations
Intron/exon structure of the chicken pyruvate kinase gene
Nils Lönberg, Walter Gilbert · Cell · 1985 · 140 citations
Isolation and characterization of the human pyruvate kinase M gene
Masaru Takenaka, Tamio Noguchi, Shigeki Sadahiro et al. · European Journal of Biochemistry · 1991 · 101 citations · Full text