Specific inactivation of inhibitory sequences in the 5′ end of the human papillomavirus type 16 L1 open reading frame results in production of high levels of L1 protein in human epithelial cells

被引:75
作者
Collier, B [1 ]
Öberg, D [1 ]
Zhao, XM [1 ]
Schwartz, S [1 ]
机构
[1] Uppsala Univ, BMC, Dept Med Biochem & Microbiol, S-75123 Uppsala, Sweden
关键词
D O I
10.1128/JVI.76.6.2739-2752.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The expression of human papillomavirus type 16 late genes encoding virus capsid proteins L1 and L2 is restricted to terminally differentiated epithelial cells in the superficial layers of the squamous epithelium. We wish to understand the molecular mechanisms that determine the levels of expression of the human papillomavirus type 16 late genes. We have previously shown that the L1 coding region contains inhibitory sequences. Here we extend previous findings to show that the 5' end of the L1 gene contains strong inhibitory sequences but that the 3' end does not. We show that the first 514 nucleotides of the L1 coding region contain multiple inhibitory elements that act independently of one another and that the major inhibitory element is located within the first 129 nucleotides of the L1 gene. Introduction of point mutations in the inhibitory elements in the 5' end of the L1 gene which altered the RNA sequence without affecting the protein sequence specifically inactivated the inhibitory elements and resulted in production of high levels of human papillomavirus type 16 L1 mRNA and protein in human epithelial cells. Furthermore, we show that inhibitory sequences are present in the L1 coding regions of multiple human papillomavirus types, demonstrating that these elements are conserved among the human papillomaviruses, and suggest that they have an important function in the viral life cycle.
引用
收藏
页码:2739 / 2752
页数:14
相关论文
共 58 条
[1]  
BAKER CC, 1997, HUMAN PAPILLOMAVIRUS, P11
[2]   DIFFERENTIATION-SPECIFIC ALTERNATIVE SPLICING OF BOVINE PAPILLOMAVIRUS LATE MESSENGER-RNAS [J].
BARKSDALE, SK ;
BAKER, CC .
JOURNAL OF VIROLOGY, 1995, 69 (10) :6553-6556
[3]  
BARKSDALE SK, 1995, MOL CELL BIOL, V15, P2962
[4]   Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases [J].
Blencowe, BJ .
TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) :106-110
[5]   A NOVEL BIPARTITE SPLICING ENHANCER MODULATES THE DIFFERENTIAL PROCESSING OF THE HUMAN FIBRONECTIN EDA EXON [J].
CAPUTI, M ;
CASARI, G ;
GUENZI, S ;
TAGLIABUE, R ;
SIDOLI, A ;
MELO, CA ;
BARALLE, FE .
NUCLEIC ACIDS RESEARCH, 1994, 22 (06) :1018-1022
[6]   Inhibitory activity of the human papillomavirus type 1 AU-rich element correlates inversely with the levels of the elav-like HuR protein in the cell cytoplasm [J].
Carlsson, A ;
Schwartz, S .
ARCHIVES OF VIROLOGY, 2000, 145 (03) :491-503
[7]   MESSENGER-RNA TRANSPORT AND HIV REV REGULATION [J].
CHANG, DD ;
SHARP, PA .
SCIENCE, 1990, 249 (4969) :614-615
[8]   2 CELLULAR PROTEINS BIND SPECIFICALLY TO A PURINE-RICH SEQUENCE NECESSARY FOR THE DESTABILIZATION FUNCTION OF A C-FOS PROTEIN-CODING REGION DETERMINANT OF MESSENGER-RNA INSTABILITY [J].
CHEN, CYA ;
YOU, Y ;
SHYU, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (12) :5748-5757
[9]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470
[10]   Translational inhibition in vitro of human papillomavirus type 16 L2 mRNA mediated through interaction with heterogenous ribonucleoprotein K and Poly(rC)-binding proteins 1 and 2 [J].
Collier, B ;
Goobar-Larsson, L ;
Sokolowski, M ;
Schwartz, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22648-22656