crta
Hrvatska znanstvena Sekcija img
bibliografija
3 gif
 Naslovna
 O projektu
 FAQ
 Kontakt
4 gif
Pregledavanje radova
Jednostavno pretraživanje
Napredno pretraživanje
Skupni podaci
Upis novih radova
Upute
Ispravci prijavljenih radova
Ostale bibliografije
Slični projekti
 Bibliografske baze podataka

Pregled bibliografske jedinice broj: 37171

Zbornik radova

Autori: Kapitanović, Sanja; Kozulić, Mirjana; Spaventi, Radan; Pavelić, Krešimir
Naslov: APC gene mutation detection by submerged gel electrophoresis of PCR fragments
Izvornik: Conference on Screeening and Early Detection of Cancer / Development of a European StrategyBeč :
Skup: Conference on Screeening and Early Detection of Cancer
Mjesto i datum: Beč, Austrija, 18-19.11.1999.
Ključne riječi: FAP; APC; germ-line mutation; mutation detection
Sažetak:
Purpose of study: Familial adenomatous polyposis (FAP) is an autosomal dominant inherited disease, affecting 1 in 2000 people. Patients with FAP develop hundreds to thousands of adenomatous polyps in the colon and rectum during their second or third decades and one or more of them progress to cancer if left without surgical treatment. Because FAP patients have a very high risk of colorectal cancer, identification of the individual risk in family members is important to prevent cancer deaths.The method of providing such accurate presymptomatic diagnosis is to determine whether a family member has inherited the particular germ-line mutation of ehe adenomatous polyposis coli (APC) gene carried by the affected parent. The majority of deletions and insertions in the APC gene were observed at positions containing repeated sequences within the coding sequence, and all caused frameshift mutations, which resulted in stop codons downstream. The most frequent germ-line mutations were found to occur at codon 1307-1311 all of which include the AAAAG 5-base-pair deletion. The frequency of this mutation reaches 24% of the total mutations previously detected. The second most frequently mutated codon 1060-1063, also contains the repeated sequence, AAAACAAAA. Other deletions also occured in the region within or near the repeated sequence (codon 1156 and 1546). variation in phenotypic expression of disease gene has been observed in FAP patients. This variation includes profuse and sparse types in respect to the number of colorectal polyps and differences in the frequency of extracolonic manifestations. The profuse type FAP patients develop more than 5000 adenomatous polyps (10 or more polyps per square cm on the colonic mucosa), and the sparse type develop fewer than 5000 of polyps. By comparing the positions of germ-line mutation of the APC gene in these two types, it was suggested that FAP patients with germ-line mutation between codon 1250 and 1464 tend to have the profuse phenotype. Method: Genomic DNA was isolated from EDTA blood. Polymerase chain reaction (PCR) was performed using specific pair of primers. PCR products were analysed by electrophoresis on a Spredex EL 300 gels. Result: After only 85 min PCR fragments of 91 and 86 bp (5 bp deletion in codon 1309) are completely resolved on a Spredex EL 300 gel. Besides the 91 bp and 86 bp fragments, in heterozygous sample there is a heteroduplex band above the 91 bp fragment. Conclusion: Electrophoresis on a Spredex gels is a simple and rapid method for determination of the most frequent germ-line mutations in the APC gene.
Vrsta sudjelovanja: Poster
Vrsta prezentacije u zborniku: Sažetak
Vrsta recenzije: Međunarodna recenzija
Projekt / tema: 00981104
Izvorni jezik: ENG
Kategorija: Znanstveni
Znanstvena područja:
Temeljne medicinske znanosti



  Verzija za printanje   za tiskati


upomoc
foot_4