Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

Telomere dynamics and genome stability in human pancreatic tumor cell line MIAPaCa-2 (CROSBI ID 141163)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Škrobot Vidaček, Nikolina ; Ćukušić, Andrea ; Ferenac Kiš, Marina ; Ivanković, Milena ; Jevtov, Irena ; Mrsić, Sanja ; Rubelj, Ivica Telomere dynamics and genome stability in human pancreatic tumor cell line MIAPaCa-2 // Cytogenetic and genome research, 119 (2007), 1-2; 60-67. doi: 10.1159/000109620

Podaci o odgovornosti

Škrobot Vidaček, Nikolina ; Ćukušić, Andrea ; Ferenac Kiš, Marina ; Ivanković, Milena ; Jevtov, Irena ; Mrsić, Sanja ; Rubelj, Ivica

engleski

Telomere dynamics and genome stability in human pancreatic tumor cell line MIAPaCa-2

Telomeres are specialized structures found at the ends of eukaryotic chromosomes serving as guardians of genome stability. In normal cells telomeres shorten with each cell division, but immortal cells undergoing multiple divisions constantly have to maintain telomere lengths above a critical level. This is accomplished either through expression of telomerase or the alternative recombination pathway (ALT). In the present study, we analyzed telomere dynamics of the telomerase positive human pancreatic tumor cell line MIAPaCa-2. The cells demonstrated genomic instability with a high frequency of chromosomal aberrations resulting in differences between individual karyotypes within the same cell population. The telomeres were short when compared with normal human fibroblasts, and about 39% of the chromosome ends did not have detectable telomere repeats as demonstrated by PNA-FISH. In many cases telomere signals were missing even when sister chromatids were strongly labeled. In addition, we used an internal PNA probe specific for the X chromosome, present in a single copy in these cells, in order to follow telomere dynamics on individual chromatids. High heterogeneity in telomere signals among individual X chromosomes as well as between their sister chromatids suggested sudden and stochastic loss or gain of telomere repeats. Such constant genomic instability often results in apoptosis and death of a fraction of cells present in the culture at all times. We discuss possible molecular mechanisms that may explain this observed telomere heterogeneity and possible adaptive repair mechanisms by which these cells maintain their chromosomes in order to survive such extreme and permanent genomic instability.

Telomere ; Telomerase ; MIAPaCa-2 ; genome stability

Rad je kao poster prezentiran na skupu 2007 Meeting on telomeres and telomerase, održanom od 02.-06.05.2007., Cold Spring Harbor, New York, SAD ; sažetak objavljen u Knjizi sažetaka, Joachim Lingner, Victoria Lundbland i Dorothy Shippen (ur.) ; 2007., str 171-171.

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

119 (1-2)

2007.

60-67

objavljeno

1424-8581

1424-859X

10.1159/000109620

Povezanost rada

Biologija

Poveznice
Indeksiranost