Downregulation of Histone Methyltransferase Genes SUV39H1 and SUV39H2 Increases Telomere Length in Embryonic Stem-like Cells and Embryonic Fibroblasts in Pigs

Telomere is a nucleoprotein structure at the ends of chromosomes that helps to protect the ends of chromosomes from being fused with other chromosomes. Knockout of histone methyltransferases Suv39h1 and Suv39h2 increases the telomere length in murine cells, whereas downregulation of SUV39H1 and SUV3...

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Veröffentlicht in:Journal of Reproduction and Development 2013, Vol.59(1), pp.27-32
Hauptverfasser: DANG-NGUYEN, Thanh Quang, HARAGUCHI, Seiki, FURUSAWA, Tadashi, SOMFAI, Tamas, KANEDA, Masahiro, WATANABE, Shinya, AKAGI, Satoshi, KIKUCHI, Kazuhiro, TAJIMA, Atsushi, NAGAI, Takashi
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Sprache:eng
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Zusammenfassung:Telomere is a nucleoprotein structure at the ends of chromosomes that helps to protect the ends of chromosomes from being fused with other chromosomes. Knockout of histone methyltransferases Suv39h1 and Suv39h2 increases the telomere length in murine cells, whereas downregulation of SUV39H1 and SUV39H2 genes decreases the telomere length in human cells, suggesting that telomere biology is different among mammalian species. However, epigenetic regulation of the telomere has not been studied in mammals other than the human and mouse. In the present study, the effect of knockdown of SUV39H1 and SUV39H2 genes on telomere length was examined in porcine embryonic stem-like cells (pESLCs) and porcine embryonic fibroblasts (PEFs). The telomeres in SUV39H1 and SUV39H2 knockdown (SUV39KD) pESLCs (37.1 ± 0.9 kb) were longer (P
ISSN:0916-8818
1348-4400
DOI:10.1262/jrd.2012-118