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
  • [1] Akao Y, 1998, CANCER RES, V58, P3773
  • [2] Proteasome-mediated proteolysis of estrogen receptor: A novel component in autologous down-regulation
    Alarid, ET
    Bakopoulos, N
    Solodin, N
    [J]. MOLECULAR ENDOCRINOLOGY, 1999, 13 (09) : 1522 - 1534
  • [3] Allis C.D., 2006, Epigenetics
  • [4] Human CpG binding protein interacts with MLL1, MLL2 and hSet1 and regulates Hox gene expression
    Ansari, Khairul I.
    Mishra, Bibhu P.
    Maedal, Subhrangsu S.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2008, 1779 (01): : 66 - 73
  • [5] Transformation of myeloid progenitors by MLL oncoproteins is dependent on Hoxa7 and Hoxa9
    Ayton, PM
    Cleary, ML
    [J]. GENES & DEVELOPMENT, 2003, 17 (18) : 2298 - 2307
  • [6] Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins
    Ayton, PM
    Cleary, ML
    [J]. ONCOGENE, 2001, 20 (40) : 5695 - 5707
  • [7] Covalent modifications of histones during development and disease pathogenesis
    Bhaumik, Sukesh R.
    Smith, Edwin
    Shilatifard, Ali
    [J]. NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (11) : 1008 - 1016
  • [8] Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae
    Briggs, SD
    Bryk, M
    Strahl, BD
    Cheung, WL
    Davie, JK
    Dent, SYR
    Winston, F
    Allis, CD
    [J]. GENES & DEVELOPMENT, 2001, 15 (24) : 3286 - 3295
  • [9] p21 is a transcriptional target of HOXA10 in differentiating myelomonocytic cells
    Bromleigh, VC
    Freedman, LP
    [J]. GENES & DEVELOPMENT, 2000, 14 (20) : 2581 - 2586
  • [10] Reduced genomic cytosine methylation and defective cellular differentiation in embryonic stem cells lacking CpG binding protein
    Carlone, DL
    Lee, JH
    Young, SRL
    Dobrota, E
    Butler, JS
    Ruiz, J
    Skalnik, DG
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (12) : 4881 - 4891