ANALYSIS OF GENETIC-HETEROGENEITY WITHIN THE TYPE STRAIN OF SATELLITE TOBACCO MOSAIC-VIRUS REVEALS SEVERAL VARIANTS AND A STRONG BIAS FOR G TO A SUBSTITUTION MUTATIONS

被引:43
作者
KURATH, G
REY, MEC
DODDS, JA
机构
[1] Department of Plant Pathology, University of California, Riverside
关键词
D O I
10.1016/0042-6822(92)90699-P
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Satellite tobacco mosaic virus (STMV) is a small plant virus that is dependent for its replication on the presence of a helper tobamovirus. RNase protection analysis of genomic RNA of the STMV type strain revealed that it was composed of two major genome types which differed at a single detectable site near nucleotide 753. Analyses of 42 full-length STMV clones for sequence heterogeneity resulted in the identification of 16 variants distinguishable by unique RNase protection assay patterns. Characterization of these variants confirmed the presence of a major heterogeneity site at nucleotide 751 and identified several sites of sequence micro heterogeneity typical of an RNA quasispecies population. Mapping of the heterogeneity sites revealed an apparently random distribution along the length of the STMV genome, with no significant clustering or preference for noncoding regions. Infectivity experiments in tobacco showed that RNA transcripts of 13 of the 16 variant clones were infectious, indicating that most of the variants represent functional genomes coexisting in the type strain with the two major genome types. Sequence analyses revealed that most of the heterogeneity sites detected, including the major site of heterogeneity, were single base differences. Assessment of all the heterogeneity sites found in the total of 10,545 nt sequenced allowed us to estimate that the RNase protection assays detected approximately 50% of the differences present in the 16 clones studied. The nature of these differences was highly biased in that 18 of the 29 single base differences characterized (62%) were G to A substitutions. © 1992.
引用
收藏
页码:233 / 244
页数:12
相关论文
共 31 条
  • [1] BIASED HYPERMUTATION OF VIRAL-RNA GENOMES COULD BE DUE TO UNWINDING MODIFICATION OF DOUBLE-STRANDED-RNA
    BASS, BL
    WEINTRAUB, H
    CATTANEO, R
    BILLETER, MA
    [J]. CELL, 1989, 56 (03) : 331 - 331
  • [2] BILLETER MA, 1991, PARAMYXOVIRUSES, P323
  • [3] BIRNBOIM HC, 1979, NUCLEIC ACIDS RES, V7, P1513
  • [4] THE QUASISPECIES (EXTREMELY HETEROGENEOUS) NATURE OF VIRAL-RNA GENOME POPULATIONS - BIOLOGICAL RELEVANCE - A REVIEW
    DOMINGO, E
    MARTINEZSALAS, E
    SOBRINO, F
    DELATORRE, JC
    PORTELA, A
    ORTIN, J
    LOPEZGALINDEZ, C
    PEREZBRENA, P
    VILLANUEVA, N
    NAJERA, R
    VANDEPOL, S
    STEINHAUER, D
    DEPOLO, N
    HOLLAND, J
    [J]. GENE, 1985, 40 (01) : 1 - 8
  • [5] Domingo E., 1988, RNA GENETICS, VIII, P3
  • [6] DUNSMUIR P, 1988, PLANT MOL BIOL MANUA, P1
  • [7] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) : 6 - 13
  • [8] BIOLOGICALLY DIVERSE MOLECULAR VARIANTS WITHIN A SINGLE HIV-1 ISOLATE
    FISHER, AG
    ENSOLI, B
    LOONEY, D
    ROSE, A
    GALLO, RC
    SAAG, MS
    SHAW, GM
    HAHN, BH
    WONGSTAAL, F
    [J]. NATURE, 1988, 334 (6181) : 444 - 447
  • [9] GOODENOW M, 1989, J ACQ IMMUN DEF SYND, V2, P344
  • [10] THE GENETIC FATE OF MOLECULARLY CLONED SIMIAN IMMUNODEFICIENCY VIRUS IN EXPERIMENTALLY INFECTED MACAQUES
    JOHNSON, PR
    HAMM, TE
    GOLDSTEIN, S
    KITOV, S
    HIRSCH, VM
    [J]. VIROLOGY, 1991, 185 (01) : 217 - 228