MLL histone methylases in gene expression, hormone signaling and cell cycle

被引:42
作者
Ansari, Khairul I. [1 ]
Mishra, Bibhu P. [1 ]
Mandal, Subhrangsu S. [1 ]
机构
[1] Univ Texas Arlington, Gene Regulat & Dis Lab, Dept Chem & Biochem, Arlington, TX 76019 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
关键词
Mixed lineage leukemia; histone methyltransferase; gene regulation; hormone signaling; cell cycle; Hox genes; Review; CPG-BINDING-PROTEIN; METHYLTRANSFERASE COMPLEX; SACCHAROMYCES-CEREVISIAE; H3; LYSINE-4; ESTROGEN-RECEPTOR; HOMEOBOX GENES; TARGET GENES; CHROMOSOMAL TRANSLOCATION; DIFFERENTIAL EXPRESSION; MAMMALIAN TRITHORAX;
D O I
10.2741/3466
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
Histone methyl-transferases (HMTs) are key enzymes that post-translationally methylate nuclear histone proteins and play critical roles in gene expression, epigenetic regulation and diseases in eukaryotic organisms. Mixed lineage leukemias (MLLs) are human HMTs that specifically methylate histone H3 at lyisine-4 and regulate gene activation. MLLs are also well known to be rearranged often in acute myeloid and lymphoid leukemias. Human encodes several MLLs that have similar enzymatic activities but diverse functions. Herein, we have reviewed the recent advances in understanding the diverse functions of MLL family of HMTs in gene regulation, hormone signaling and cell cycle regulation in human.
引用
收藏
页码:3483 / 3495
页数:13
相关论文
共 93 条
  • [61] QIAN K, 2005, SHENG LI XUE BAO, V57, P498
  • [62] Compromised HOXA5 function can limit p53 expression in human breast tumours
    Raman, V
    Martensen, SA
    Reisman, D
    Evron, E
    Odenwald, WF
    Jaffee, E
    Marks, J
    Sukumar, S
    [J]. NATURE, 2000, 405 (6789) : 974 - 978
  • [63] Gene regulation - Code of silence
    Rice, JC
    Allis, CD
    [J]. NATURE, 2001, 414 (6861) : 258 - +
  • [64] The Saccharomyces cerevisiae Set1 complex includes an Ash2 homologue and methylates histone 3 lysine 4
    Roguev, A
    Schaft, D
    Shevchenko, A
    Pijnappel, WWMP
    Wilm, M
    Aasland, R
    Stewart, AF
    [J]. EMBO JOURNAL, 2001, 20 (24) : 7137 - 7148
  • [65] MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia
    Ruault, M
    Brun, ME
    Ventura, M
    Roizès, G
    De Sario, A
    [J]. GENE, 2002, 284 (1-2) : 73 - 81
  • [66] Histone H3 recognition and presentation by the WDR5 module of the MLL1 complex
    Ruthenburg, Alexander J.
    Wang, Wooikoon
    Graybosch, Daina M.
    Li, Haitao
    Allis, C. David
    Patel, Dinshaw J.
    Verdine, Gregory L.
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (08) : 704 - 712
  • [67] Methylation of histone H3K4 mediates association of the Isw1p ATPase with chromatin
    Santos-Rosa, H
    Schneider, R
    Bernstein, BE
    Karabetsou, N
    Morillon, A
    Weise, C
    Schreiber, SL
    Mellor, J
    Kouzarides, T
    [J]. MOLECULAR CELL, 2003, 12 (05) : 1325 - 1332
  • [68] DIFFERENTIAL EXPRESSION OF HOMEOBOX GENES IN FUNCTIONALLY DISTINCT CD34(+) SUBPOPULATIONS OF HUMAN BONE-MARROW CELLS
    SAUVAGEAU, G
    LANSDORP, PM
    EAVES, CJ
    HOGGE, DE
    DRAGOWSKA, WH
    REID, DS
    LARGMAN, C
    LAWRENCE, HJ
    HUMPHRIES, RK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) : 12223 - 12227
  • [69] Histone H2B ubiquitylation controls processive methylation but not monomethylation by Dot1 and Set1
    Shahbazian, MD
    Zhang, KL
    Grunstein, M
    [J]. MOLECULAR CELL, 2005, 19 (02) : 271 - 277
  • [70] A requirement for the Saccharomyces cerevisiae Paf1 complex in snoRNA 3′ end formation
    Sheldon, KE
    Mauger, DM
    Arndt, KM
    [J]. MOLECULAR CELL, 2005, 20 (02) : 225 - 236