SEQUENCES HOMOLOGOUS TO 5' SPLICE SITES ARE REQUIRED FOR THE INHIBITORY ACTIVITY OF PAPILLOMAVIRUS LATE 3' UNTRANSLATED REGIONS

被引:129
作者
FURTH, PA
CHOE, WT
REX, JH
BYRNE, JC
BAKER, CC
机构
[1] NCI, TUMOR VIRUS BIOL LAB, BETHESDA, MD 20892 USA
[2] UNIV MARYLAND, SCH MED, DEPT MED, DIV INFECT DIS, BALTIMORE, MD 21201 USA
关键词
D O I
10.1128/MCB.14.8.5278
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of bovine papillomavirus type 1 (BPV-1) tate genes is limited to terminally differentiated keratinocytes in an infected epithelium. We have previously shown that although the BPV-1 late polyadenylation site is functional in nonpermissive cells, a 53-nucleotide (nt) fragment of the late 3' untranslated region acts posttranscriptionally to reduce polyadenylated cytoplasmic RNA levers. This 53-nt fragment does not appear to function by destabilizing polyadenylated cytoplasmic RNA (P. A. Furth and C. C. Baker, J. Virol. 65:5806-5812, 1991). In this study, we used site-directed mutagenesis and deletion analysis to demonstrate that the sequence AAG/GUAAGU, which is identical to the consensus 5' splice site sequence, was both necessary and sufficient for the inhibitory activity of the 53-nt fragment. Furthermore, base pairing between the 5' end of the U1 small nuclear RNA and this 5' splice site-like sequence was shown to be required for the inhibitory activity in vivo. We have also further mapped the human papillomavirus type 16 late 3' inhibitory element (I. M. Kennedy, J. K. Haddow, and J. B. Clements, J. Virol. 65:2093-2097, 1991) to a 51-nt region containing four overlapping sequence motifs with partial homology to 5' splice sites. Mutation of each of these motifs demonstrated that only one of these motifs is required for the inhibitory activity. However, the presence of the other motifs may contribute to the full inhibitory activity of the element. No BPV-1 or human papillomavirus type 16 mRNAs which are spliced by using the potential 5' splice sites present in the viral late 3' untranslated regions have been identified. This suggests that the primary function of these 5' splice site-like sequences is the inhibition of late gene expression. The most likely mechanism of action of these elements is reduction of polyadenylation efficiency, perhaps through interference with 3'-terminal exon definition.
引用
收藏
页码:5278 / 5289
页数:12
相关论文
共 87 条
  • [71] SPALHOLZ BA, 1989, ADV VIRAL ONCOL, V8, P27
  • [72] MESSENGER-RNAS FROM THE TRANSFORMING REGION OF BOVINE PAPILLOMA-VIRUS TYPE-I
    STENLUND, A
    ZABIELSKI, J
    AHOLA, H
    MORENOLOPEZ, J
    PETTERSSON, U
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1985, 182 (04) : 541 - 554
  • [73] EFFECT OF 5' SPLICE SITE MUTATIONS ON SPLICING OF THE PRECEDING INTRON
    TALERICO, M
    BERGET, SM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) : 6299 - 6305
  • [74] CHARACTERIZATION OF THE MOUSE BETA-MAJ GLOBIN TRANSCRIPTION TERMINATION REGION - A SPACING SEQUENCE IS REQUIRED BETWEEN THE POLY(A) SIGNAL SEQUENCE AND MULTIPLE DOWNSTREAM TERMINATION ELEMENTS
    TANTRAVAHI, J
    ALVIRA, M
    FALCKPEDERSEN, E
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) : 578 - 587
  • [75] THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 POLYADENYLYLATION SIGNAL - A 3' LONG TERMINAL REPEAT ELEMENT UPSTREAM OF THE AAUAAA NECESSARY FOR EFFICIENT POLYADENYLYLATION
    VALSAMAKIS, A
    ZEICHNER, S
    CARSWELL, S
    ALWINE, JC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) : 2108 - 2112
  • [76] ELEMENTS UPSTREAM OF THE AAUAAA WITHIN THE HUMAN-IMMUNODEFICIENCY-VIRUS POLYADENYLATION SIGNAL ARE REQUIRED FOR EFFICIENT POLYADENYLATION INVITRO
    VALSAMAKIS, A
    SCHEK, N
    ALWINE, JC
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (09) : 3699 - 3705
  • [77] A COMPLEX SECONDARY STRUCTURE IN U1A PREMESSENGER RNA THAT BINDS 2 MOLECULES OF U1A PROTEIN IS REQUIRED FOR REGULATION OF POLYADENYLATION
    VANGELDER, CWG
    GUNDERSON, SI
    JANSEN, EJR
    BOELENS, WC
    POLYCARPOUSCHWARZ, M
    MATTAJ, IW
    VANVENROOIJ, WJ
    [J]. EMBO JOURNAL, 1993, 12 (13) : 5191 - 5200
  • [78] ASSOCIATION WITH TERMINAL EXONS IN PREMESSENGER RNAS - A NEW ROLE FOR THE U1 SNRNP
    WASSARMAN, KM
    STEITZ, JA
    [J]. GENES & DEVELOPMENT, 1993, 7 (04) : 647 - 659
  • [79] EFFECT OF SODIUM-BUTYRATE ON INDUCTION OF CELLULAR AND VIRAL-DNA SYNTHESES IN POLYOMA VIRUS-INFECTED MOUSE KIDNEY-CELLS
    WAWRA, E
    POCKL, E
    MULLNER, E
    WINTERSBERGER, E
    [J]. JOURNAL OF VIROLOGY, 1981, 38 (03) : 973 - 981
  • [80] POLY(A) SITE EFFICIENCY REFLECTS THE STABILITY OF COMPLEX-FORMATION INVOLVING THE DOWNSTREAM ELEMENT
    WEISS, EA
    GILMARTIN, GM
    NEVINS, JR
    [J]. EMBO JOURNAL, 1991, 10 (01) : 215 - 219