The alternative splicing factor hnRNP A1 is up-regulated during virus-infected epithelial cell differentiation and binds the human papillomavirus type 16 late regulatory element

• Published in: Virus research Vol. 131; no. 2; pp. 189 - 198
• Main Authors: Cheunim, Thanaporn, Zhang, Jingxin, Milligan, Steven G., McPhillips, Maria G., Graham, Sheila V.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-02-2008; Elsevier Science
• Subjects: Alternative splicing; Cell Line; DNA, Viral - metabolism; Electrophoretic Mobility Shift Assay; Epithelial Cells - virology; Heterogeneous Nuclear Ribonucleoprotein A1; Heterogeneous-Nuclear Ribonucleoprotein Group A-B - biosynthesis; Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism; hnRNP A1; HPV16; Human papillomavirus 16; Human papillomavirus 16 - genetics; Humans; Organ Culture Techniques; Protein Binding; Regulatory Elements, Transcriptional; RNA processing; Up-Regulation; Alternative splicing; ESS; hnRNP A1; GST; SF2/ASF; U1snRNP; HPV16; NHK; SR proteins; 3′ UTR; RBD; EMSA; CAT; RNA processing; LRE
• ISSN: 0168-1702; 1872-7492
• DOI: 10.1016/j.virusres.2007.09.006

Human papillomavirus type 16 (HPV16) infects anogenital epithelia and is the etiological agent of cervical cancer. We showed previously that HPV16 infection regulates the key splicing/alternative splicing factor SF2/ASF and that virus late transcripts are extensively alternatively spliced. hnRNP A1 is the antagonistic counterpart of SF2/ASF in alternative splicing. We show here that hnRNP A1 is also up-regulated during differentiation of virus-infected epithelial cells in monolayer and organotypic raft culture. Taken together with our previous data on SF2/ASF, this comprises the first report of HPV-mediated regulation of expression of two functionally related cellular proteins during epithelial differentiation. Further, using electrophoretic mobility shift assays and UV crosslinking we demonstrate that hnRNP A1 binds the HPV16 late regulatory element (LRE) in differentiated HPV16 infected cells. The LRE has been shown to be important in temporally controlling virus late gene expression during epithelial differentiation. We suggest that increased levels of these cellular RNA processing factors facilitate appropriate alternative splicing necessary for production of virus late transcripts in differentiated epithelial cells.