Study on genetic variability at alpha sub (s1) and alpha sub (s2) casein loci in autochthonous goat populations of the Lombardy Alps

[The polymorphism at alpha sub (s1)- and alpha sub (s2)-casein loci on genomic DNA of 284 Bionda dell´Adamello and Lariana breed goats was studied by PCR. Twenty six genotype combinations were observed; the most frequent combination is CSN1S sup (FF)/CSN1S2 sup (AA) (44.4%), whose alleles at both lo...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Italian journal of animal science 2003, Vol.2
Hauptverfasser: Meggiolaro, D. (Milan Univ. (Italy). Istituto di Zootecnia Generale), Marilli, M. (Milan Univ. (Italy). Istituto di Zootecnia Generale), Ramelli, P. (Milan Univ. (Italy). Istituto di Zootecnia Generale), Milani, D. (Milan Univ. (Italy). Istituto di Zootecnia Generale), Crepaldi, P. (Milan Univ. (Italy). Istituto di Zootecnia Generale)
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[The polymorphism at alpha sub (s1)- and alpha sub (s2)-casein loci on genomic DNA of 284 Bionda dell´Adamello and Lariana breed goats was studied by PCR. Twenty six genotype combinations were observed; the most frequent combination is CSN1S sup (FF)/CSN1S2 sup (AA) (44.4%), whose alleles at both loci are the most frequent (69.7 and 88.2%). All the other combinations have very low frequencies, starting from CSN1S1 sup (EF)/CSN1S2 sup (AA) (12.7%). In 237 subjects with informative haplotypes (homozygous for at least one locus), haplotypes CSN1S1 sup (F)/CSN1S2 sup (B) and CSN1S1 sup (0)/CSN1S2 sup (A) are less frequent than expected, while haplotype CSN1S1 sup (0)/CSN1S2 sup (B) is more frequent than expected (P0.05).] E´ stato studiato il polimorfismo ai loci alfa inf (s1)- e alfa inf (S2)-caseina, tramite PCR, su DNA genomico di 284 capre di razza Bionda dell´Adamello e Lariana. Sono state osservate 26 combinazioni genotipiche, tra le quali la più frequente è CSN1S sup (FF)/CSN1S2 sup (AA) (44,4%), i cui alleli ai due loci sono i più diffusi (69,7 e 88,2%). Tutte le altre combinazioni sono molto meno frequenti, a partire da CSN1S1 sup (EF)/CSN1S2 sup (AA) con il 12,7%. In 237 soggetti con aplotipi informativi (omozigoti ad almeno uno dei due loci), si è rilevato che gli aplotipi CSN1S1 sup (F)/CSN1S2 sup (B) e CSN1S1 sup (0)/CSN1S2 sup (A) sono meno frequenti dell´atteso, mentre l´aplotipo CSN1S1 sup (0)/CSN1S2 sup (B) è più frequente dell´atteso (P0,05)
ISSN:1594-4077
1828-051X