Highly conserved prion protein sequences in random bred cats with three novel synonymous PRNP gene variants


Akış Akad I., Güven C.

TOPICS IN COMPANION ANIMAL MEDICINE, cilt.68, ss.1-7, 2025 (SCI-Expanded, Scopus) identifier identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 68
  • Basım Tarihi: 2025
  • Doi Numarası: 10.1016/j.tcam.2025.101006
  • Dergi Adı: TOPICS IN COMPANION ANIMAL MEDICINE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Agricultural & Environmental Science Database, CAB Abstracts, MEDLINE, Veterinary Science Database
  • Sayfa Sayıları: ss.1-7
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Evet

Özet

Transmissible spongiform encephalopathies are infectious, fatal, neurodegenerative diseases that affect both

humans and animals. They occur as a result of misfolding of prion protein. In some species, variations in prion

protein gene (PRNP) were associated with susceptibility to prion diseases. To date, only a few studies have

investigated prion protein in cats. For this reason, this study aims to identify feline PRNP polymorphisms in

random-bred cats. DNA isolation, PCR and 922 bp amplicon sequencing were performed in order to detect PRNP

gene variants in 74 cat samples collected from Istanbul, north-western part of Turkey. Results were evaluated by

using SPSS 25.0, HAPLOTYPE ANALYSIS 1.05, DnaSP v6, SRPLOT and PHYLOVIZ Online. In total, eleven

polymorphisms including 10 SNPs and a 27 bp in/del polymorphism in the tandem repeat region were observed.

Three of these SNPs, c.201C>A, c.225C>T, c.228A>C, were detected for the first time. All SNPs in the open

reading frame were synonymous, so no amino acid variation was detected in the prion protein sequence. A total

of 28 haplotypes were observed, including 8 major haplotypes with frequencies ≥ 0.05. The results indicating

that the prion protein is conserved in cats from north-western Turkey, in contrast to other samples from this

country, point to possible differences in the PRNP gene between relatively closely located populations.