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J Gen Virol 73 (1992), 3147-3153; DOI 10.1099/0022-1317-73-12-3147
© 1992 Society for General Microbiology

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Rearrangements of the upstream regulatory region of human papillomavirus type 6 can be found in both Buschke-Löwenstein tumours and in condylomata acuminata

Albert Rübben1, Sylvie Beaudenon2, Michel Favre2, Wolfgang Schmitz1, Bettina Spelten1 and Elke-Ingrid Grussendorf-Conen1

1 Hautklinik (Department of Dermatology) der RWTH-Aachen, Pauwelsstrasse 30, 5100 Aachen, Germany
and2 Unité des Papillomavirus, Unité de l'Institut National de la Santé et de la Recherche Médicale 190, Institut Pasteur, 75015 Paris, France

Clinically malignant Buschke-Löwenstein tumours and benign condylomata acuminata are caused by human papillomaviruses (HPVs), predominantly HPV-6 and -11. In some cases, the HPV-6 genomes found in Buschke-Löwenstein tumours and in verrucous carcinomas differ from HPV-6b isolated from a benign genital wart, by rearrangements of the upstream regulatory region (URR). To evaluate the frequency and role of mutations of the URR of HPV-6 we analysed 42 condylomata acuminata and four Buschke-Löwenstein tumours by the polymerase chain reaction and restriction enzyme cleavage. Using only four different restriction enzymes we could demonstrate four distinct restriction patterns, indicating that naturally occurring HPV-6 isolates display a high degree of DNA polymorphism within the URR. One Buschke-Löwenstein tumour and two condylomata acuminata yielded rearranged URRs with DNA duplications. All three lesions harboured multiple HPV-6 variants, suggesting that cellular or environmental factors facilitate the development of rearrangements. Therefore, rearrangements of the URR may represent only secondary events in condylomata acuminata and Buschke-Löwenstein tumours which do not necessarily confer a higher malignant potential to the infected cell.

Received 22 July 1992; accepted 24 August 1992.


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R. Kovelman, G. K. Bilter, A. Roman, D. R. Brown, and M. S. Barbosa
Human papillomavirus type 6: classification of clinical isolates and functional analysis of E2 proteins
J. Gen. Virol., September 1, 1999; 80(9): 2445 - 2451.
[Abstract] [Full Text]




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