Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease

被引:227
作者
Mehler, Mark F. [1 ]
Mattick, John S.
机构
[1] Albert Einstein Canc Ctr, Dept Neurol & Neurol Sci, Inst Brain Disorders & Neural Regenerat, Bronx, NY 10461 USA
[2] Albert Einstein Canc Ctr, Dept Psychiat & Behav Sci, Inst Brain Disorders & Neural Regenerat, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Rose F Kennedy Ctr Res Mental Retardat & Dev Disa, Bronx, NY 10461 USA
[4] Univ Queensland, Inst Mol Biosci, ARC Special Res Ctr Funct & Appl Genom, St Lucia, Qld, Australia
关键词
D O I
10.1152/physrev.00036.2006
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Mehler MF, Mattick JS. Noncoding RNAs and RNA Editing in Brain Development, Functional Diversification, and Neurological Disease. Physiol Rev 87: 799-823, 2007; doi:10.1152/physrev.00036.2006.-The progressive maturation and functional plasticity of the nervous system in health and disease involve a dynamic interplay between the transcriptome and the environment. There is a growing awareness that the previously unexplored molecular and functional interface mediating these complex gene-environmental interactions, particularly in brain, may encompass a sophisticated RNA regulatory network involving the twin processes of RNA editing and multifaceted actions of numerous subclasses of non-protein-coding RNAs. The mature nervous system encompasses a wide range of cell types and interconnections. Long-term changes in the strength of synaptic connections are thought to underlie memory retrieval, formation, stabilization, and effector functions. The evolving nervous system involves numerous developmental transitions, such as neurulation, neural tube patterning, neural stem cell expansion and maintenance, lineage elaboration, differentiation, axonal path finding, and synaptogenesis. Although the molecular bases for these processes are largely unknown, RNA-based epigenetic mechanisms appear to be essential for orchestrating these precise and versatile biological phenomena and in defining the etiology of a spectrum of neurological diseases. The concerted modulation of RNA editing and the selective expression of non-protein-coding RNAs during seminal as well as continuous state transitions may comprise the plastic molecular code needed to couple the intrinsic malleability of neural network connections to evolving environmental influences to establish diverse forms of short and long-term memory, context-specific behavioral responses, and sophisticated cognitive capacities.
引用
收藏
页码:799 / 823
页数:25
相关论文
共 316 条
  • [101] Phylogenetic reconstruction of orthology, paralogy, and conserved synteny for dog and human
    Goodstadt, Leo
    Ponting, Chris P.
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2006, 2 (09) : 1134 - 1150
  • [102] Sex-linked period genes in the silkmoth, Antheraea pernyi:: Implications for circadian clock regulation and the evolution of sex chromosomes
    Gotter, AL
    Levine, JD
    Reppert, SM
    [J]. NEURON, 1999, 24 (04) : 953 - 965
  • [103] 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
  • [104] Regulation of heterochromatin by histone methylation and small RNAs
    Grewal, SIS
    Rice, JC
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (03) : 230 - 238
  • [105] Negative regulation of neural stem/progenitor cell proliferation by the Pten tumor suppressor gene in vivo
    Groszer, M
    Erickson, R
    Scripture-Adams, DD
    Lesche, R
    Trumpp, A
    Zack, JA
    Kornblum, HI
    Liu, X
    Wu, H
    [J]. SCIENCE, 2001, 294 (5549) : 2186 - 2189
  • [106] ALU-ring elements in the primate genomes
    Grover, D
    Kannan, K
    Brahmachari, SK
    Mukerji, M
    [J]. GENETICA, 2005, 124 (2-3) : 273 - 289
  • [107] FMR2 function: insight from a mouse knockout model
    Gu, Y
    Nelson, DL
    [J]. CYTOGENETIC AND GENOME RESEARCH, 2003, 100 (1-4) : 129 - 139
  • [108] Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island
    Gu, YH
    Shen, Y
    Gibbs, RA
    Nelson, DJ
    [J]. NATURE GENETICS, 1996, 13 (01) : 109 - 113
  • [109] Recent advances in fragile X: a model for autism and neurodegeneration
    Hagerman, RJ
    Ono, MY
    Hagerman, PJ
    [J]. CURRENT OPINION IN PSYCHIATRY, 2005, 18 (05) : 490 - 496
  • [110] Hardiman KE, 2002, GENETICS, V161, P231