Vox Sanguinis

While screening Le(a+b+) Polynesian DNA samples for a candidate Sew allele, a point mutation (C5”+T) resulting in a new stop codon (Arg19’+stop) in the a( 1,2)fucosyltransferase gene (FUT2) was identified. This point mutation resulted in the gaining of a new restriction enzyme cleavage site (DdeI), which allowed restriction enzyme cleavage screening of 40 selected Polynesians and 42 random Caucasians. The nonsecretor phenotype in two of the three nonsecretor Polynesians analyzed was due to homozygosity for the ‘new’ mutation, whereas the third Polynesian nonsecretor (with Caucasian ancestors) was due to homozygosity of the ‘old’ (Tq~’~~+stop) mutation. The nonsecretor phenotype in all Caucasians analyzed was a consequence of homozygosity for the ‘old’ mutation. Both the new and the old nonsecretor mutations were identified in the heterozygous state in some secretor-positive Polynesians, while only the old mutation was found in the heterozygous state in Caucasians of the same phenotype. .....................

[1]  L. Svensson,et al.  DNA Sequencing and Screening for Point Mutations in the Human Lewis (FUT3) Gene Enables Molecular Genotyping of the Human Lewis Blood Group System , 1996, Vox sanguinis.

[2]  R. Oriol,et al.  Lewis Histo‐Blood Group System and Associated Secretory Phenotypes , 1995, Vox sanguinis.

[3]  G. Lennon,et al.  Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype. , 1995, The Journal of biological chemistry.

[4]  R. Oriol,et al.  Expression of Lewis histo-blood group glycolipids in the plasma of individuals of Le(a+b+) and partial secretor phenotypes , 1994, Glycoconjugate Journal.

[5]  R. Oriol,et al.  Immunochemical and immunohistological expression of Lewis histo-blood group antigens in small intestine including individuals of the Le(a+b+) and Le(a−b−) nonsecretor phenotypes , 1994, Glycoconjugate Journal.

[6]  R. Oriol,et al.  Detection and Characterization of Lewis Antigens in Plasma of Lewis‐Negative Individuals Evidence of Chain Extension as a Result of Reduced Fucosyltransferase Competition , 1994, Vox sanguinis.

[7]  J. Lowe,et al.  Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[8]  D. Woodfield,et al.  Investigation of Lewis Phenotypes in Polynesians: Evidence of a Weak Secretor Phenotype , 1990, Vox sanguinis.

[9]  Shirley A. Miller,et al.  A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.

[10]  J. Le Pendu,et al.  The presence of at least two different H-blood-group-related beta-D-gal alpha-2-L-fucosyltransferases in human serum and the genetics of blood group H substances. , 1985, American journal of human genetics.

[11]  T. Kumazaki,et al.  Biochemical evidence that secretor gene, Se, is a structural gene encoding a specific fucosyltransferase. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[12]  R. Oriol,et al.  A new genetic model proposing that the Se gene is a structural gene closely linked to the H gene. , 1981, American journal of human genetics.

[13]  P. Mollison,et al.  Progress in Hematology , 1957 .

[14]  R. Oriol ABO, Hh, Lewis, and Secretion , 1995 .

[15]  R. E. Broadberry,et al.  The Lewis blood group system among Chinese in Taiwan. , 1991, Human heredity.

[16]  W. Watkins Biochemistry and Genetics of the ABO, Lewis, and P blood group systems. , 1980, Advances in human genetics.

[17]  P. Comley,et al.  Red cell and saliva studies for the evaluation of ABH and Lewis factors among the Caucasian and Aboriginal populations of Western Australia. , 1967, Acta genetica et statistica medica.