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Journal of Virology, July 2001, p. 6121-6134, Vol. 75, No. 13
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.13.6121-6134.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
p21cip1 Degradation in Differentiated Keratinocytes Is Abrogated
by Costabilization with Cyclin E Induced by Human Papillomavirus
E7
Francisco
Noya,
Wei-Ming
Chien,
Thomas R.
Broker, and
Louise T.
Chow*
Department of Biochemistry and Molecular
Genetics, University of Alabama at Birmingham, Birmingham, Alabama
35294-0005
Received 2 April 2001/Accepted 9 April 2001
The human papillomavirus (HPV) E7 protein promotes S-phase reentry
in a fraction of postmitotic, differentiated keratinocytes. Here we
report that these cells contain an inherent mechanism that opposes
E7-induced DNA replication. In organotypic raft cultures of primary
human keratinocytes, neither cyclin E nor p21cip1 is detectable in
situ. However, E7-transduced differentiated cells not in S phase
accumulate abundant cyclin E and p21cip1. We show that normally p21cip1
protein is rapidly degraded by proteasomes. In the presence of E7 or
E6/E7, p21cip1, cyclin E, and cyclin E2 proteins were all up-regulated.
The accumulation of p21cip1 protein is a posttranscriptional event, and
ectopic cyclin E expression was sufficient to trigger it. In constract,
cdk2 and p27kip1 were abundant in normal differentiated cells and were
not significantly affected by E7. Cyclin E, cdk2, and p21cip1 or
p27kip1 formed complexes, and relatively little kinase activity was
found associated with cyclin E or cdk2. In patient papillomas and E7
raft cultures, all p27kip1-positive cells were negative for
bromodeoxyuridine (BrdU) incorporation, but only some also contained
cyclin E and p21cip1. In contrast, all cyclin E-positive cells also
contained p27kip1. When the expression of p21cip1 was reduced by
rottlerin, a PKC
inhibitor, p27kip1- and BrdU-positive cells
remained unchanged. These observations show that high levels of
endogenous p27kip1 can prevent E7-induced S-phase reentry. This
inhibition then leads to the stabilization of cyclin E and p21cip1.
Since efficient initiation of viral DNA replication requires cyclin E
and cdk2, its inhibition accounts for heterogeneous viral activities in productively infected lesions.
*
Corresponding author. Mailing address: Department of
Biochemistry and Molecular Genetics, University of Alabama at
Birmingham, 510 McCallum Basic Health Sciences Bldg., 1918 University
Blvd., Birmingham, AL 35294-0005. Phone: (205) 975-8300. Fax: (205)
975-6075. E-mail: ltchow{at}uab.edu.
Journal of Virology, July 2001, p. 6121-6134, Vol. 75, No. 13
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.13.6121-6134.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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