Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

Identification and phytogeny of the human endogenous retrovirus HERV-W LTR Family in Cancer Cells

Animal Cells and Systems 2002³â 6±Ç 2È£ p.167 ~ 170
ÀÌÁÖ¹Ì, ±èȯ¹¬, ±èÈñ¼ö,
¼Ò¼Ó »ó¼¼Á¤º¸
ÀÌÁֹ̠( Yi Joo-Mi ) - Pusan National University College of Natural Sciences Division of Biological Sciences
±èȯ¹¬ ( Kim Hwan-Mook ) - Korea Research Institute of Bioscience and Biotechnology
±èÈñ¼ö ( KIM HEUI-SOO ) - Pusan National University College of Natural Sciences Division of Biological Sciences

Abstract


The long terminal repeats (LTRs) of human endogenous retrovirus (HERV) have been found to be coexpressed with sequences of closely located genes. It has been suggested that the LTR elements have contributed to the structural change or genetic variation of human genome connected to various diseases and evolution. We examined the HERV?W LTR elements in various cancer cells (2F7, A431, A549, HepG2, MIA?PaCa?2, PC?3, RT4, SiHa, U?937, and UO?31). Using genomic DNA from the cancer cells, we performed PCR amplification and identified twelve new HERV?W LTR elements. Those LTR elements showed a high degree of sequence similarity (88?99%) with HERV?W LTR (A F072500). A phylogenetic tree obtained by the neighbor?joining method revealed that HERV?W LTR elements could be mainly divided into two groups through evolutionary divergence. Three HERV?W LTR elements (RT4?2, A431?1, and UO31?2) belonged to Group I, whereas nine LTR elements (2F7?2, A549?1, A549?3, HepG2?3, MP2?2, PC3?1, SiHa?8, SiHa?10, and U937?1) belonged to Group D. Taken together, our new sequence data of the HERV?W LTR elements may contribute to an understanding of tissue?specific cancer by genomic instability of LTR integration.

Ű¿öµå

Cancer cells; HERV?W; LTR elements; Phylogeny

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

µîÀçÀú³Î Á¤º¸