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    Isolation and Phylogeny of HERV-W pol Fragments in Human monochromosomes

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    https://www.riss.kr/link?id=A3364755

    • 저자

      Jeon,Seung Heui (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Yi,Joo Mi (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Shin,Kyung Mi (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Lee,Ji Won (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Hong,Kyung Won (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Huh,Jae Won (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Jung,A Ram (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Choi,Jin (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Lee,Won Ho (Division of Biological Sciences,College of Natural Sciences,Pusan National University) ;  Kim,Heui Soo (Division of Biological Sciences,College of Natural Sciences,Pusan National University)

    • 발행기관
    • 학술지명
    • 권호사항
    • 발행연도

      2001

    • 작성언어

      English

    • KDC

      470.000

    • 자료형태

      학술저널

    • 발행기관 URL
    • 수록면

      98-98(1쪽)

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    다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

    A new human endogenous retroviral family (HERV-W) has recently been described that is related to multiple sclerosis-associated retrovirus (MSRV) sequences that have been identified in particles recovered from monocyte cultures from patients with multiple sclerosis. Using the PCR approach with human monochromosomal somatic cell hybrid DNA panel, twenty-four pol fragments of HERV-W family from chromosomes 2, 3, 4, 5, 6, 7, 8, 10, 11, 12, 13, 14, 15, 20, 21, X, and Y were identified and analyzed. They showed a high degree of nucleotide sequence similarity (89.3-91.3%) with that of the HERV-W. Translation of the pol fragments showed no frameshift and termination codon by deletion/insertion or point mutation in some clones, HWP4-1; HWP4-2 from chromosome 4, and HWPX-1 from chromosome X. Phylogenetic analysis from the HERV-W family indicates that the pol fragments has evolved independently among chromosomes or represent integration events separately during primate evolution.
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    A new human endogenous retroviral family (HERV-W) has recently been described that is related to multiple sclerosis-associated retrovirus (MSRV) sequences that have been identified in particles recovered from monocyte cultures from patients with multi...

    A new human endogenous retroviral family (HERV-W) has recently been described that is related to multiple sclerosis-associated retrovirus (MSRV) sequences that have been identified in particles recovered from monocyte cultures from patients with multiple sclerosis. Using the PCR approach with human monochromosomal somatic cell hybrid DNA panel, twenty-four pol fragments of HERV-W family from chromosomes 2, 3, 4, 5, 6, 7, 8, 10, 11, 12, 13, 14, 15, 20, 21, X, and Y were identified and analyzed. They showed a high degree of nucleotide sequence similarity (89.3-91.3%) with that of the HERV-W. Translation of the pol fragments showed no frameshift and termination codon by deletion/insertion or point mutation in some clones, HWP4-1; HWP4-2 from chromosome 4, and HWPX-1 from chromosome X. Phylogenetic analysis from the HERV-W family indicates that the pol fragments has evolved independently among chromosomes or represent integration events separately during primate evolution.

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