FELINE IMMUNODEFICIENCY VIRUS GENE-EXPRESSION - ANALYSIS OF THE RNA SPLICING PATTERN AND THE MONOCISTRONIC REV MESSENGER-RNA

被引:29
作者
TOMONAGA, K
SHIN, YS
FUKASAWA, M
MIYAZAWA, T
ADACHI, A
MIKAMI, T
机构
[1] UNIV TOKYO,FAC AGR,DEPT VET MICROBIOL,BUNKYO KU,TOKYO 113,JAPAN
[2] NAGASAKI UNIV,INST TROP MED,DEPT PREVENT MED,NAGASAKI 852,JAPAN
[3] KYOTO UNIV,INST VIRUS RES,DEPT VIRAL ONCOL,SAKYO KU,KYOTO 606,JAPAN
关键词
D O I
10.1099/0022-1317-74-11-2409
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The transcription pattern of the feline immunodeficiency virus (FIV) genome in a feline CD4+ cell line was examined. In addition to the genomic RNA (9.2 kb), at least five FIV-specific transcripts [5-2, 4.4 (doublet), 1-7 and 1.4 kb] were detected by using subgenomic restriction enzyme fragments of an FIV molecular clone or FIV-specific oligonucleotides as probes. Among these transcripts, the 9.2, 5.2 and 4.4 (doublet) kb mRNAs were not expressed in the cytoplasm of cells transfected with a rev- mutant. To determine the location of splice junctions in the FIV genome, we used PCR to amplify and clone cDNAs corresponding to the viral mRNAs from infected cells. The region between pol and env was found to contain at least two splice donor and three splice acceptor sites. Two splice acceptor sites were detected in the 3' region of env. By hybridization analysis and sequencing of cDNA clones, it was revealed that the medium sized mRNAs are derived from a single splice event, with different splice acceptor sites, and that the two smaller transcripts are doubly or triply spliced mRNAs. Our results demonstrate a complex pattern of alternative splicing of FIV mRNAs. Furthermore, we identified monocistronic rev mRNA species that employ a unique splice acceptor site.
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页码:2409 / 2417
页数:9
相关论文
共 34 条
[1]   PRODUCTION OF ACQUIRED IMMUNODEFICIENCY SYNDROME-ASSOCIATED RETROVIRUS IN HUMAN AND NONHUMAN CELLS TRANSFECTED WITH AN INFECTIOUS MOLECULAR CLONE [J].
ADACHI, A ;
GENDELMAN, HE ;
KOENIG, S ;
FOLKS, T ;
WILLEY, R ;
RABSON, A ;
MARTIN, MA .
JOURNAL OF VIROLOGY, 1986, 59 (02) :284-291
[3]   A NOVEL HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEIN, TEV, SHARES SEQUENCES WITH TAT, ENV, AND REV PROTEINS [J].
BENKO, DM ;
SCHWARTZ, S ;
PAVLAKIS, GN ;
FELBER, BK .
JOURNAL OF VIROLOGY, 1990, 64 (06) :2505-2518
[4]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[5]   REGULATORY PATHWAYS GOVERNING HIV-1 REPLICATION [J].
CULLEN, BR ;
GREENE, WC .
CELL, 1989, 58 (03) :423-426
[6]   CHARACTERIZATION OF A CDNA CLONE ENCODING THE VISNA VIRUS TRANSACTIVATING PROTEIN [J].
DAVIS, JL ;
CLEMENTS, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (02) :414-418
[7]   VISNA VIRUS EXHIBITS A COMPLEX TRANSCRIPTIONAL PATTERN - ONE ASPECT OF GENE-EXPRESSION SHARED WITH THE ACQUIRED-IMMUNODEFICIENCY-SYNDROME RETROVIRUS [J].
DAVIS, JL ;
MOLINEAUX, S ;
CLEMENTS, JE .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1325-1331
[8]   REV ACTIVATES EXPRESSION OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 VIF-GENE AND VPR-GENE PRODUCTS [J].
GARRETT, ED ;
TILEY, LS ;
CULLEN, BR .
JOURNAL OF VIROLOGY, 1991, 65 (03) :1653-1657
[9]  
ISHIDA T, 1989, J AM VET MED ASSOC, V194, P221
[10]   IDENTIFICATION OF FELINE IMMUNODEFICIENCY VIRUS REV GENE ACTIVITY [J].
KIYOMASU, T ;
MIYAZAWA, T ;
FURUYA, T ;
SHIBATA, R ;
SAKAI, H ;
SAKURAGI, JI ;
FUKASAWA, M ;
MAKI, N ;
HASEGAWA, A ;
MIKAMI, T ;
ADACHI, A .
JOURNAL OF VIROLOGY, 1991, 65 (08) :4539-4542