VIRUS-ENCODED CYCLIN

被引:118
作者
JUNG, JU
STAGER, M
DESROSIERS, RC
机构
[1] New England Reg. Primate Res. Center, Harvard Medical School, Southborough
[2] New England Reg. Primate Res. Center, Harvard Medical School, Southborough, MA 01772-9102, One Pine Hill Dr.
关键词
D O I
10.1128/MCB.14.11.7235
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
Herpesvirus saimiri contains an open reading frame called eclf2 with homology to the cellular type D cyclins. We now show that the eclf2 gene product is a novel virus-encoded cyclin (v-cyclin). The protein encoded by the v-cyclin gene of this oncogenic herpesvirus was found to have an apparent molecular size of 29 kDa in transformed cells. v-Cyclin protein was found to be associated with cdk6, a cellular cyclin-dependent kinase known to interact with cellular type D cyclins. cdk6/v-cyclin complexes strongly phosphorylated Rb fusion protein and histone H1 as substrates in vitro. Mutational analyses showed that highly conserved amino acids in the cyclin box of v-cyclin were important for association with cdk6 and for activation of cdk6 kinase activity. Thus, v-cyclin resembles cellular type D cyclins in primary sequence, in its association with cdk6, by its ability to activate protein kinase activity, and by the presence of functional cyclin box sequences. v-Cyclin exhibited a selective preference for association with cdk6 over other cyclin-dependent kinases and a high level of kinase activation. The properties of v-cyclin suggest a likely role in oncogenic transformation by this T-lymphotropic herpesvirus.
引用
收藏
页码:7235 / 7244
页数:10
相关论文
共 45 条
  • [1] PRIMARY STRUCTURE OF THE HERPESVIRUS SAIMIRI GENOME
    ALBRECHT, JC
    NICHOLAS, J
    BILLER, D
    CAMERON, KR
    BIESINGER, B
    NEWMAN, C
    WITTMANN, S
    CRAXTON, MA
    COLEMAN, H
    FLECKENSTEIN, B
    HONESS, RW
    [J]. JOURNAL OF VIROLOGY, 1992, 66 (08) : 5047 - 5058
  • [2] BATES S, 1994, ONCOGENE, V9, P71
  • [3] STABLE GROWTH TRANSFORMATION OF HUMAN LYMPHOCYTES-T BY HERPESVIRUS SAIMIRI
    BIESINGER, B
    MULLERFLECKENSTEIN, I
    SIMMER, B
    LANG, G
    WITTMANN, S
    PLATZER, E
    DESROSIERS, RC
    FLECKENSTEIN, B
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (07) : 3116 - 3119
  • [4] CULLEN BR, 1987, METHOD ENZYMOL, V152, P684
  • [5] NONONCOGENIC DELETION MUTANTS OF HERPESVIRUS SAIMIRI ARE DEFECTIVE FOR INVITRO IMMORTALIZATION
    DESROSIERS, RC
    SILVA, DP
    WALDRON, LM
    LETVIN, NL
    [J]. JOURNAL OF VIROLOGY, 1986, 57 (02) : 701 - 705
  • [6] PHYSICAL INTERACTION OF THE RETINOBLASTOMA PROTEIN WITH HUMAN D-CYCLINS
    DOWDY, SF
    HINDS, PW
    LOUIE, K
    REED, SI
    ARNOLD, A
    WEINBERG, RA
    [J]. CELL, 1993, 73 (03) : 499 - 511
  • [7] ASSOCIATION OF HUMAN CYCLIN-E WITH A PERIODIC G(1)-S PHASE PROTEIN-KINASE
    DULIC, V
    LEES, E
    REED, SI
    [J]. SCIENCE, 1992, 257 (5078) : 1958 - 1961
  • [8] FUNCTIONAL INTERACTIONS OF THE RETINOBLASTOMA PROTEIN WITH MAMMALIAN D-TYPE CYCLINS
    EWEN, ME
    SLUSS, HK
    SHERR, CJ
    MATSUSHIME, H
    KATO, JY
    LIVINGSTON, DM
    [J]. CELL, 1993, 73 (03) : 487 - 497
  • [9] FLECKENSTEIN B, 1982, HERPESVIRUSES, V1, P253
  • [10] A 60 KD CDC2-ASSOCIATED POLYPEPTIDE COMPLEXES WITH THE E1A PROTEINS IN ADENOVIRUS-INFECTED CELLS
    GIORDANO, A
    WHYTE, P
    HARLOW, E
    FRANZA, BR
    BEACH, D
    DRAETTA, G
    [J]. CELL, 1989, 58 (05) : 981 - 990