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Human CytomegalovirusÀÇ ÇüÁúÀüȯÀ¯ÀüÀÚ(mtr¥±) Morphological Transformation Region ¥±(mtr¥±) of Human Cytomegalovirus

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½Å¿¬¸í/Yeon Myung Shin ¼Õ¼ö»ó/°­Áß½Å/À强ÀÍ/ÀÌÀÎȯ/Soo Sang Sohn/Joong Shin Kang/Sung Ik Chang/In Hwan Lee

Abstract

¼­·Ð
Herpes ¹ÙÀÌ·¯½º°è´Â µÎ °¡´ÚÀÇ DNA·Î ±¸¼ºµÇ´Â ¼±»ó±¸Á¶·Î¼­ 120¡­230 kbÀÇ Å©±â·Î
À̽ʸéü ÇÇ°¢¼Ó¿¡ ÇÇ°³ ¹× ¿ÜÇÇ·Î µÑ·¯½Î¿© ÀÖ´Ù À̵éÀº ¼÷ÁÖÀÇ Á¾·ù, ¼¼Æ÷º´¸®, »ý½ÄÁÖ±â
ÀÇ ±æÀÌ ¹× Àẹ °¨¿°µÇ´Â ¼¼Æ÷ÀÇ Á¾·ù¿¡ µû¶ó ºÐ·ùµÇ¸ç herpes simplex 1Çü°ú 2Çü(HSV-1,
HSV-2), varicella zoster virus(VZV), Epstein Barr virus(EBV), human cytomegalovirus
(ÀÌÇÏ HCMV), human B lymphotrophic virus(HBLV) ¹× human herpes virus 7Çü(HHV-7)
ÀÌÀÌ¿¡ ¼ÓÇÑ´Ù. HCMV´Â »õ·Î¿î ¸í¸í¹ý¿¡ µû¶ó HHV-5·Î ºÒ¸®¿öÁö±âµµ ÇÑ´Ù. HCMV´Â
1956³â ¼¼Æ÷ºñ´ë¼ººÀÀÔüº´ ȯÀÚÀÇ Ä§»ù¿¡¼­ ºÐ¸®µ¿Á¤µÇ¾úÀ¸¸ç, °¨¿° Ãʱ⿡´Â ÀϹÝÀûÀ¸·Î
Áõ»óÀÌ ¾ø´Â °æ¿ì°¡ º¸ÅëÀ̳ª ´Ü±¸Áõ Áõ»óÀÌ ÀÖÀ» ¼ö ÀÖ´Ù. ÀÌ ¹ÙÀÌ·¯½ºÀÇ °¨¿°Àº ¾î¸± ¶§
ºÎÅÍ ÀϾ¸ç ÀϹÝÀÎÀÇ 40¡­100%¿¡¼­ º¸Ã¼°áÇÕÇ×ü¸¦ °¡Á® °ú°Å°¨¿°ÀÇ ÈçÀûÀ» º¸ÀδÙ.
230 kbÀÇ Å©±â¿¡ ÇØ´çÇÏ´Â HCMV´Â ¥â-herpesvirinase¿¡ ¼ÓÇÏ¸ç ´ÊÀº »ý½ÄÁֱ⸦ °¡Áø
´Ù. ¶Ç ¹Ýº¹¼­¿­(repeat sequence)ÀÇ Æ¯Â¡À¸·Î ¿ªÀ§(inverted repeat)ÀÎ terminal repeat
long(TRL)°ú infernal repeat long(IRL)À» °¡Á® HSV-1°ú HSV-2¿Í ÇÔ²² ¼¼ ¹ø° ±º¿¡ ¼ÓÇÑ
´Ù. HCMV¿¡ °¨¿°µÈ ÈÄ Àẹ±â¿¡´Â ºÐºñ¼±(secretory gland), ¸²ÇÁ¸Á»ó¼¼Æ÷, ½ÅÀåµî¿¡¼­ ¹ß
°ßµÇ¸ç, À¯°üÇÑ Á¾¾çÀ¸·Î´Â ÀڱðæºÎ¾Ï, Àü¸³¼± ¼±Á¾, ´ëÀåÀÇ ¼±Á¾ ¹× Kaposi¾¾ À°Á¾ µîÀÌ
¾Ë·ÁÁ® ÀÖ´Ù. ƯÈ÷ Kaposi¾¾ À°Á¾ÀÇ °æ¿ì ȯÀÚ¿¡¼­ anti-HCMV Ç×ü°¡ ¾ÆÁÖ ³ô°Ô ÃøÁ¤µÇ¾î
HCMV°¡ ÀÌ À°Á¾ÀÇ ¹ÙÀÌ·¯½º º¸Á¶ÀÎÀÚ·Î ¿©°ÜÁö°í ÀÖ´Ù. ƯÈ÷ ¿©±â¼­ ºÐ¸®µÈ K9V Á¾ÁÖ´Â
»ç¶÷ÀÇ Ç÷°ü³»ÇǼ¼Æ÷¸¦ ÇüÁúÀüȯ½Ãų¼ö ÀÖ´Â °ÍÀ¸·Î º¸°íµÇ¾î ÀÖ¾î Kaposi¾¾ À°Á¾ Çü¼º¿¡
Áß¿äÇÑ ÀÎÀÚ·Î ¾Ë·ÁÁ® ÀÖ´Ù. ±× ¹ÛÀÇ Á¾¾ç¿¡¼­µµ ¹ÙÀÌ·¯½º°¡ ºÐ¸®µÇ°Å³ª HCMVÀÇ DNA °¡
´ÚÀÌ Southern blot hybridizationÀ¸·Î µ¿Á¤µÇ¾ú´Ù.
ÀÌ ¹ÙÀÌ·¯½ºÀÇ ÇüÁúÀüȯ¿¡ °üÇÑ º¸°í·Î´Â ¿©·¯ ¼³Ä¡·ù ¹× »ç¶÷ÀÇ ¼¼Æ÷¹è¾ç¿¡¼­ ÀÌ·ç¾îÁ³
´Ù Àڿܼ±À¸·Î ºÒÈ°¼ºÈ­ ½ÃŲ HCMV Á¾ÁÖ C-87Àº hamster embryoÀÇ ¼¶À¯¾Æ¼¼Æ÷¸¦ ¹ÌºÐ
È­µÈ ¾Ç¼º À°Á¾À¸·Î ÇüÁúÀüȯ½ÃÄ×À¸¸ç, Á¾ÁÖ Mj´Â ÅÂ¾Æ Æó¼¼Æ÷ ¹è¾ç¿¡¼­ ÇüÁúÀüȯÀ» ÀÏÀ¸ÄÑ
nude mice¿¡¼­ Á¾¾ç ¹ß»ý´ÉÀ» º¸¿´´Ù. ±×·¯³ª ¹è¾ç¼¼Æ÷¿¡¼­ ÇüÁúÀüȯµÈ ¼¼Æ÷°¡ º¯È­µÈ ¸ð¾ç
À» °è´ë¹è¾çÀ» ÅëÇØ °è¼Ó À¯ÁöÇÏ´Â ¹Ý¸é¿¡ HCMVÀÇ Æ¯ÀÌÇ¥Áö, Áïviral-specific DNA,
HCMV-encoded antigen µîÀÌ ¼Ò½ÇµÇ¾î HCMVÀÇ °¨¿°°ú ÇüÁúÀüȯ°úÁ¤ÀÇ ¿¬°è¼³¸íÀÌ ½±Áö
¾Ê´Ù. 1982³â NelsonµîÀº HCMV strain AD 169 DNA¸¦ Hind¥² ȤÀº Xba I È¿¼Ò·Î Àý´ÜÇÑ
µÚ ¼¼Æ÷¿¡ µµÀÔÇÏ¿© ÇüÁúÀüȯÀ» À¯µµÇÏ¿´´Ù. Áï È¿¼Ò¿¡ ÀÇÇØ Àý´ÜµÈ ¹ÙÀÌ·¯½º DNA ÀýÆíÀÌ
ÇüÁúÀüȯ´ÉÀ» °è¼Ó °¡Áø´Ù´Â °ÍÀÌ ÀÔÁõµÇ¾ú´Ù. 2.9kb Xbal/Hind¥² DNA ÀýÆíÀÌ cosmid
vector¿Í ¼¼Æ÷³»¿¡ µµÀԵǸé ÇüÁúÀüȯ´ÉÀ» °¡Áö°ÔµÇ¾î ÇüÅÂÀüȯ¿µ¿ª I(morphological
transforming region I;ÀÌÇÏ mtrI)·Î ¸í¸íÇÏ¿´´Ù(Fig. 1). ±×·¯³ª mtrlÀ¸·Î ÀÎÇÑ ´Ü¹éÁúÀÌ ¾ø
À¸¸ç º¯ÇüµÈ ¼¼Æ÷³ª Á¾¾ç¿¡¼­ À¯·¡µÈ ¼¼Æ÷ÁÖ¿¡¼­ mtrIÀÇ DNA ¹è¿­ÀÌ ¹ß°ßµÇÁö ¾Ê¾Æ mtrI
Àº ¼¼Æ÷¾ÏÀ¯ÀüÀÚÀÇ Àü»ç¸¦ Áõ°­½ÃÅ°°Å³ª ¼¼Æ÷ DNA¿¡ »ðÀÔµÊÀ¸·Î¼­ ÀϾ´Â º¯ÀÌ·Î ¾Ë·Á
Á³´Ù. HCMVÀÇ µÎ¹ø° ÇüÅÂÀüȯ¿µ¿ª(mtr¥±)Àº TowneÁ¾ÁÖ¿¡¼­ ºÐ¸®µÇ¾úÀ¸¸ç Xbal È¿¼Òó
¸®¿¡¼­ EÀýÆí¿¡ ÇØ´çµÈ´Ù(Fig. 1). ÀÌ XbaI-EÀýÆíÀº 20kb Á¤µµÀ̸ç hamster ¹è¾Æ¼¼Æ÷¸¦ ºÒ
¸êÈ­ ½ÃÅ°¸ç NIH3T3 ¼¼Æ÷¸¦ ÇüÁúÀüȯ½ÃÄ×´Ù. ±×ÈÄÀÌ E ÀýÆÝÀº µÎ°³ÀÇ ÇüÅÂÀüȯ¿µ¿ªÀ» °¡
Áö´Â °ÍÀÌ ¾Ë·ÁÁ® XbaI/BamHI 3.0 kb EM ÀýÆíÀ» mtr¥±, BamHI/ XbaI 7.6 kb EM ÀýÆíÀ»
mtr¥²À¸·Î À̸§ Áö¿öÁ³´Ù. ±×·¯³ª mtr¥²Àº HCMVÆí À¯·¡µÈ ¼¼Æ÷ÁÖ È¤Àº Á¾¾ç¿¡¼­ mtr¥²ÀÇ
Àü»ç¼­¿­ÀÌ ¾ø¾î Á÷Á¢ÀûÀÎ ÇüÅÂÀüȯ¿µ¿ªÀÎÁö´Â ºÒÈ®½ÇÇÏ´Ù.
À̷μ­ HCMV·Î À¯µµ·Î ºÒ¸êÈ­µÈ ¼¼Æ÷ÁÖ¿¡¼­ mtr¥±ÀÇ Á¸Àç°¡ º¯ÇüÀ» À¯ÁöÇϴµ¥ Áß¿äÀÎ
ÀÚ·Î ¿©°ÜÁö¸ç subclone ºÐ¼®À¸·Î´Â ÃÖ¼Ò¿µ¿ªÀ¸·Î 980bpÀÇ Ban¥±/XhoI ÀýÆíÀÌ º¸°íµÇ¾ú´Ù.
ÀÌ Ban¥±/XhoI ÀýÆíÀ» ¼­¿­ºÐ¼®ÇÏ¸é ¼¼°³ÀÇ open reading frame (ÀÌÇÏ ORF)ÀÌ ÀÖÀ¸¸ç ÀÌ
´Â °¢°¢ 79, 83, 34°³ÀÇ ¾Æ¹Ì³ë»êÀ» ¸¸µé¾î ³»°í(coding) ÀÖ¾î 790RF, 830RF, 340RF¶ó ĪÇÑ
´Ù(Fig. 2).
980 bp Å©±âÀÇ Ban¥±/Xhoi ÀýÆíÀÎ mtr¥±Àº Bgl¥² È¿¼Ò·Î Àý´ÜµÇ´Â À§Ä¡°¡ ÀÖÀ¸¸ç ÀÌ°Í
Àº 790RF DNA¼Ó¿¡ À־ mtr¥± DNA¸¦ ÀÌ È¿¼Ò·Î Àý´ÜÇÏ¸é µÎ°³ÀÇ DNA ÀýÆíÀÌ ¾ò¾îÁö
´Âµ¥ ¿ÂÀüÇÑ °Í°ú µÎ ÀýÆíÀ» NIH3T3 ¼¼Æ÷¿¡ µµÀÔÇÏ¿© 790RFÀÇ º¯Çü´ÉÀ» È®ÀÎÇÏ°íÀÚ ÇÏ¿´
´Ù.
#ÃÊ·Ï#
Purpose : Human herpesviruses have been associated with the etiology of several
human cancers. The role of these viruses in carcinogenesis has not yet been clarified.
This study focused on identifying and characterizing the transforming potential of cloned
DNA fragments from human cytomegalovirus (HCMV).
Materials and Methods : Multiple DNA fragments of HCMV were applied to cells for
transformation. Morphological transforming region ¥±(mtr¥±) of HCMV strain Towne has
been identified to a 3.0kb XbaI-BamHl DNA fragment which was retained in
transformed cells. The transforming activity was induced by a 980 bp Ball-B(ho I
subfragment(pBS980) containing both promoter/regulatory elements as well as three open
reading frames(ORFs), i.e.,790RF, 830RF, and 340RF. The ORFs have been evaluated for
transforming potential in NIH3T3 cells.
Results : Mtr¥±(pBS980) has Bg¥² restriction enzyme site which divides into two
subfragments, pBS440 and pBS540, the latter has whole 830RF, 340RF, and fragment of
790RF, the former has only fragment of 790RF. Among three ORFs, 830RF and 340RF
were not functional in transformation, because in pBS540 these ORFs were not
truncated.
Conclusion : The 790RF(79-aa transforming peptide) has allowed a better approach to
determine the role of HCMV in human carcinogenesis.

Å°¿öµå

Human cytomegalovirus; Morphological transformation region(mar);

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