http://www.cnr.it/ontology/cnr/individuo/prodotto/ID175811
Short communication: The β-casein (CSN2) silent allele C1 is highly spread in goat breeds (Articolo in rivista)
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- Short communication: The β-casein (CSN2) silent allele C1 is highly spread in goat breeds (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.3168/jds.2008-1228 (literal)
- Alternative label
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- Stefania Chessa; Daniela Rignanese; Julia Küpper; Giulio Pagnacco; Georg Erhardt; Anna Caroli (literal)
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- Stefania Chessa, Daniela Rignanese, Giulio Pagnacco - Dipartimento di Sclenze e Tecnologie Veterinarie per la Sicurezza Alimentare, Università degli Studi dl Milano, Via Trentacoste 2, Milano, 20134, Italy;
Julia Küpper, Georg Erhardt - Institut für Tierzucht und Haustiergenetik, Justus-Liebig-Universität, Ludwigstr. 21 b, 35390 Gießen, Germany;
Anna Caroli - Dipartimento di Scienze Biomediche e Blotecnologle, Università degli Studi di Brescia, Viale Europa 11, Brescia, 25123, Italy (literal)
- Titolo
- Short communication: The β-casein (CSN2) silent allele C1 is highly spread in goat breeds (literal)
- Abstract
- Several single nucleotide polymorphisms have been identified in the goat milk casein genes, most of them modifying the amino acid sequence of the coded protein. At least 9 variants have been found in goat β-CN (CSN2); 6 of them were characterized at the DNA level (A, A1, C, E, 0, and 0'), whereas the other 3 variants were described only at the protein level. The recently identified silent Al allele is characterized by a C->T transition at the 180th nucleotide of the ninth exon. In the present work, typing results from different breeds (3 Italian, 3 German, and a composite of African breeds for a total of 335 samples) demonstrated that the same mutation is carried by the CSN2*C allele. In addition, the T nucleotide at the 180th nucleotide of the ninth exon was always associated with CSN2*C in all the breeds analyzed. Thus, another silent allele occurs at goat CSN2 and can be named CSN2*C1. The much wider distribution of C1 with respect to the A1 allele indicates that the single nucleotide polymorphisms characterizing the silent mutation originated from CSN2*C. A method for the identification of this allele simultaneously with 5 of the 6 DNA-characterized alleles is also proposed. The mutation involved codifies for the same protein of the C allele; nevertheless, its location in the 3' untranslated region of the gene might affect the specific casein expression. (literal)
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