MicroRNA biogenesis and cancer

被引:525
作者
Gregory, RI
Shiekhattar, R
机构
[1] Wistar Inst Anat & Biol, Gene Express & Regulat Program, Philadelphia, PA 19104 USA
[2] Wistar Inst Anat & Biol, Mol Cellular & Oncogenesis Program, Philadelphia, PA 19104 USA
关键词
D O I
10.1158/0008-5472.CAN-05-0298
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNA) are a recently discovered family of short non-protein-coding RNAs that negatively regulate gene expression. Recent studies of miRNAs highlight a requirement for cell viability. Posttranscriptional silencing of target genes by miRNAs occurs either by targeting specific cleavage of homologous mRNAs, or by targeting specific inhibition of protein synthesis. We recently identified a multisubunit protein complex termed Microprocessor that is necessary and sufficient for processing miRNA precursor RNAs. Microprocessor contains Drosha, an RNase III endonuclease, and DGCR8, a gene deleted in DiGeorge syndrome. We consider recent findings that link miRNA perturbation to cancer.
引用
收藏
页码:3509 / 3512
页数:4
相关论文
共 22 条
  • [1] Human microRNAs are processed from capped, polyadenylated transcripts that can also function as mRNAs
    Cai, XZ
    Hagedorn, CH
    Cullen, BR
    [J]. RNA, 2004, 10 (12) : 1957 - 1966
  • [2] Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia
    Calin, GA
    Dumitru, CD
    Shimizu, M
    Bichi, R
    Zupo, S
    Noch, E
    Aldler, H
    Rattan, S
    Keating, M
    Rai, K
    Rassenti, L
    Kipps, T
    Negrini, M
    Bullrich, F
    Croce, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) : 15524 - 15529
  • [3] Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers
    Calin, GA
    Sevignani, C
    Dan Dumitru, C
    Hyslop, T
    Noch, E
    Yendamuri, S
    Shimizu, M
    Rattan, S
    Bullrich, F
    Negrini, M
    Croce, CM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) : 2999 - 3004
  • [4] Processing of primary microRNAs by the Microprocessor complex
    Denli, AM
    Tops, BBJ
    Plasterk, RHA
    Ketting, RF
    Hannon, GJ
    [J]. NATURE, 2004, 432 (7014) : 231 - 235
  • [5] The Microprocessor complex mediates the genesis of microRNAs
    Gregory, RI
    Yan, KP
    Amuthan, G
    Chendrimada, T
    Doratotaj, B
    Cooch, N
    Shiekhattar, R
    [J]. NATURE, 2004, 432 (7014) : 235 - 240
  • [6] The Drosha-DGCR8 complex in primary microRNA processing
    Han, JJ
    Lee, Y
    Yeom, KH
    Kim, YK
    Jin, H
    Kim, VN
    [J]. GENES & DEVELOPMENT, 2004, 18 (24) : 3016 - 3027
  • [7] The human DiGeorge syndrome critical region gene 8 and its D-melanogaster homolog are required for miRNA biogenesis
    Landthaler, M
    Yalcin, A
    Tuschl, T
    [J]. CURRENT BIOLOGY, 2004, 14 (23) : 2162 - 2167
  • [8] The nuclear RNase III Drosha initiates microRNA processing
    Lee, Y
    Ahn, C
    Han, JJ
    Choi, H
    Kim, J
    Yim, J
    Lee, J
    Provost, P
    Rådmark, O
    Kim, S
    Kim, VN
    [J]. NATURE, 2003, 425 (6956) : 415 - 419
  • [9] MicroRNA genes are transcribed by RNA polymerase II
    Lee, Y
    Kim, M
    Han, JJ
    Yeom, KH
    Lee, S
    Baek, SH
    Kim, VN
    [J]. EMBO JOURNAL, 2004, 23 (20) : 4051 - 4060
  • [10] MicroRNA maturation: stepwise processing and subcellular localization
    Lee, Y
    Jeon, K
    Lee, JT
    Kim, S
    Kim, VN
    [J]. EMBO JOURNAL, 2002, 21 (17) : 4663 - 4670