Pregled bibliografske jedinice broj: 1184382
Identification of monomorphic and polymorphic genes associated with recessive fertility defects in Holstein cows reared in Kazakhstan
Identification of monomorphic and polymorphic genes associated with recessive fertility defects in Holstein cows reared in Kazakhstan // Veterinarski arhiv, 92 (2022), 1; 27-35 doi:10.24099/vet.arhiv.1390 (međunarodna recenzija, članak, znanstveni)
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Naslov
Identification of monomorphic and polymorphic
genes associated with recessive fertility defects
in Holstein cows reared in Kazakhstan
Autori
Ussenbekov, Yessengali ; Bagdat, Aigerim ; Bimenova, Zhanat ; Orynkhanov, Kanat ; Sobiech, Przemysław ; Samardžija, Marko ; Chandra, S. Pareek ; Dobos, Attila
Izvornik
Veterinarski arhiv (0372-5480) 92
(2022), 1;
27-35
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
loss of fertility ; mutations ; SNP ; genetic defects ; haplotypes ; PCR-RFLP ; APAF1 ; HH1 ; SMC2 ; HH3 ; GART ; HH4 ; HCD ; APOB ; Holstein cow
Sažetak
Haplotypes of candidate genes namely: apoptotic protease activating factor 1 (APAF1 p.Q579X or HH1), glycinamide ribonucleotide formyltransferase (GART or HH4), structural maintenance of chromosomes 2 (SMC2 or HH3), and haplotype cholesterol deficiency (HCD) genes associated with recessive fertility defects (loss of fertility) were investigated in imported Canadian Holstein cows reared at “Medeu Commerce” LLP breeding farm in Kazakhstan. The genotypic profiling of the APAF1/HH1, GART/HH4 fertility haplotype carriers was carried out by PCR-RFLP methods using BstC8I and Tru9I and MseI, while the genotypic profiling of the SMC2/HH3, and HCD fertility haplotype carriers was carried out using our own primer designed by internal primer marker methods. The study revealed that the PCR-RFLP diagnostic markers APAF1/HH1 and GART/HH4 for recessive fertility defects were monomorphic in the Canadian Holstein cows investigated. However, the diagnostic markers SMC2/HH3 and HCD fertility haplotype carriers (our own design diagnostic markers) were polymorphic, with frequencies of 3% and 11%, respectively, in the investigated Canadian Holstein cows. The study concluded that genetic monitoring of recessive fertility defects enables the timely identification of carriers of harmful lethal mutations, and control of the fertility haplotype elimination process.
Izvorni jezik
Engleski
Znanstvena područja
Veterinarska medicina
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
Uključenost u ostale bibliografske baze podataka::
- BIOSIS Previews (Biological Abstracts)
- CAB Abstracts
- Zoological Record
- FISHLIT