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Allelic diversity of the human plasma α(1,3)fucosyltransferase gene ( FUT6 )
Author(s) -
PANG H.,
KODA Y.,
SOEJIMA M.,
SCHLAPHOFF T.,
TOIT E. D.,
KIMURA H.
Publication year - 1999
Publication title -
annals of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 77
eISSN - 1469-1809
pISSN - 0003-4800
DOI - 10.1046/j.1469-1809.1999.6340277.x
Subject(s) - genetics , allele , xhosa , biology , null allele , loss of heterozygosity , gene , genetic diversity , coding region , population , demography , philosophy , linguistics , sociology
The 1080‐bp coding region of the human plasma α(1,3)fucosyltransferase gene ( FUT6 ) was sequenced in a total of 161 individuals (322 chromosomes) drawn from three populations, involving 56 Africans (Xhosa), 52 European‐Africans of South Africa, and 53 Japanese. In addition to six reported base substitutions, eleven new base substitutions and a single base insertion were found in the coding region of the FUT6 . Eleven functional and four null alleles were encountered, of which 10 alleles were novel alleles identified in this study. Two null alleles have been identified previously, whereas two novel null alleles, which contained a single base (cytosine) insertion at nucleotide 499, were found in a Xhosa population. The allelic distributions of FUT6 were different among these three populations. The heterozygosity of FUT6 was 0.860, 0.699, and 0.632, in Xhosa, European‐African (South Africa), and in Japanese populations, respectively. The extensive DNA sequence diversity of the FUT6 may be suitable for application as a tool in genetic studies for modern human evolution.