Controlling the elongation phase of transcription with P-TEFb

被引:888
作者
Peterlin, B. Matija [1 ]
Price, David H.
机构
[1] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
[2] Univ Calif San Francisco, Rosalind Russell Med Res Ctr, Dept Med Microbiol & Immunol, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.molcel.2006.06.014
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
The positive transcription elongation factor b(P-TEFb) is a cyclin-dependent kinase that controls the elongation phase of transcription by RNA polymerase II (RNAPII). This process is made possible by the reversal of effects of negative elongation factors that include NELF and DSIF. In complex organisms, elongation control is critical for the regulated expression of most genes. In those organisms, the function of P-TEFb is influenced negatively by HEXIM proteins and 7SK snRNA and positively by a variety of recruiting factors. Phylogenetic analyses of the components of the human elongation control machinery indicate that the number of mechanisms utilized to regulate P-TEFb function increased as organisms developed more complex developmental patterns.
引用
收藏
页码:297 / 305
页数:9
相关论文
共 98 条
  • [11] CHODOSH LA, 1989, J BIOL CHEM, V264, P2250
  • [12] Transcription-dependent association of multiple positive transcription elongation factor units to a HEXIM multimer
    Dulac, C
    Michels, AA
    Fraldi, A
    Bonnet, F
    Nguyen, VT
    Napolitano, G
    Lania, L
    Bensaude, O
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (34) : 30619 - 30629
  • [13] Myc recruits P-TEFb to mediate the final step in the transcriptional activation of the cad promoter
    Eberhardy, SR
    Farnham, PJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (42) : 40156 - 40162
  • [14] Regulation of polymerase II transcription by 7SK snRNA: Two distinct RNA elements direct P-TEFb and HEXIM1 binding
    Egloff, S
    Van Herreweghe, E
    Kiss, T
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (02) : 630 - 642
  • [15] Relief of two built-in autoinhibitory mechanisms in P-TEFb is required for assembly of a multicomponent transcription elongation complex at the human immunodeficiency virus type 1 promoter
    Fong, YW
    Zhou, Q
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (16) : 5897 - 5907
  • [16] Stimulatory effect of splicing factors on transcriptional elongation
    Fong, YW
    Zhou, Q
    [J]. NATURE, 2001, 414 (6866) : 929 - 933
  • [17] Cyclin K functions as a CDK9 regulatory subunit and participates in RNA polymerase II transcription
    Fu, TJ
    Peng, JM
    Lee, G
    Price, DH
    Flores, O
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) : 34527 - 34530
  • [18] Dynamics of human immunodeficiency virus transcription: P-TEFb phosphorylates RD and dissociates negative effectors from the transactivation response element
    Fujinaga, K
    Irwin, D
    Huang, YH
    Taube, R
    Kurosu, T
    Peterlin, BM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (02) : 787 - 795
  • [19] CDK9 autophosphorylation regulates high-affinity binding of the human immunodeficiency virus type 1 Tat-P-TEFb complex to TAR RNA
    Garber, ME
    Mayall, TP
    Suess, EM
    Meisenhelder, J
    Thompson, NE
    Jones, KA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (18) : 6958 - 6969
  • [20] The interaction between HIV-1 Tat and human cyclin T1 requires zinc and a critical cysteine residue that is not conserved in the murine CycT1 protein
    Garber, ME
    Wei, P
    KewalRamani, VN
    Mayall, TP
    Herrmann, CH
    Rice, AP
    Littman, DR
    Jones, KA
    [J]. GENES & DEVELOPMENT, 1998, 12 (22) : 3512 - 3527