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Characterization and genetic analysis of bovine α s1 ‐casein I variant
Author(s) -
Lühken G.,
Caroli A.,
IbeaghaAwemu E. M.,
Erhardt G.
Publication year - 2009
Publication title -
animal genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 81
eISSN - 1365-2052
pISSN - 0268-9146
DOI - 10.1111/j.1365-2052.2009.01861.x
Subject(s) - biology , genetics , genotyping , exon , single nucleotide polymorphism , casein , polymorphism (computer science) , genotype , breed , gene , haplotype , food science
Summary The aim of this study was to identify the molecular genetic origin underlying the I variant of α s1 ‐casein and to develop a DNA‐based test for this polymorphism as a tool for genetic analyses independent of milk sample testing. All coding exons and flanking regions of the α s 1 ‐casein gene were sequenced in DNA samples from cattle of known α s 1 ‐casein genotypes ( BI , CI , II , CC ), determined by isoelectric focusing of milk samples. A nucleotide substitution (A>T) in exon 11 (g.19836A>T) leads to the exchange of Glu with Asp at amino acid position 84 of the mature protein (p.Glu84Asp) and perfectly co‐segregated with the presence of the α s1 ‐casein I variant in the milk of the analysed animals. Genotyping of a total of 680 DNA samples from 31 Bos taurus and Bos indicus cattle breeds and from Bos grunniens , Bison bison and Bison bonasus by restriction fragment length polymorphism analysis revealed the occurrence of Asp at position 84 at low frequencies in Bos taurus and Bos indicus breeds and established its origin from the α s1 ‐casein C variant (p.Glu192Gly). Ten different intragenic haplotypes in the gene region from intron 8 to intron 12 were observed by sequencing, of which two occurred in Bison bison and one in Bison bonasus only. Using available casein gene complex information, an association of Asp at position 84 to β‐casein A 2 and κ‐casein B was shown in the Bos indicus breed Banyo Gudali . Taken together, we can postulate that the α s1 ‐casein variant I is caused by a non‐synonymous nucleotide substitution in exon 11 of the gene and that it originated within Bos indicus and spread to Bos taurus subsequently.