Summary: | <p>Abstract</p> <p>Background</p> <p>Human papillomavirus type 16 (HPV-16) E5 protein co-operates with epidermal growth factor to stimulate mitogenesis of murine fibroblasts. Currently, little is known about which viral amino acids are involved in this process. Using sequence variants of HPV-16 E5 we have investigated their effects upon E5 transcription, cell-cycling and cell-growth of murine fibroblasts.</p> <p>Results</p> <p>We demonstrate that: (i) introduction of Thr<sup>64 </sup>into the reference E5 sequence of HPV-16 abrogates mitogenic activity: both were poorly transcribed in NIH-3T3 cells; (ii) substitution of Leu<sup>44</sup>Val<sup>65 </sup>or, Thr<sup>37</sup>Leu<sup>44</sup>Val<sup>65 </sup>into the HPV-16 E5 reference backbone resulted in high transcription in NIH-3T3 cells, enhanced cell-cycle progression and high cell-growth; and, (iii) inclusion of Tyr<sup>8 </sup>into the Leu<sup>44</sup>Val<sup>65 </sup>backbone inhibited E5 induced cell-growth and repression of p21 expression, despite high transcription levels.</p> <p>Conclusion</p> <p>The effects of HPV-16 E5 variants upon mitosis help to explain why Leu<sup>44</sup>Val<sup>65 </sup>HPV-16 E5 variants are most prevalent in 'wild' pathogenic viral populations in the UK.</p>
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