Protection of p27Kip1 mRNA by quaking RNA binding proteins promotes oligodendrocyte differentiation

[1]  D. Rowitch Glial specification in the vertebrate neural tube , 2004, Nature Reviews Neuroscience.

[2]  T. Schedl,et al.  Translation repression by GLD-1 protects its mRNA targets from nonsense-mediated mRNA decay in C. elegans. , 2004, Genes & development.

[3]  James M. Roberts,et al.  p27Kip1 modulates cell migration through the regulation of RhoA activation. , 2004, Genes & development.

[4]  C. ffrench-Constant,et al.  Mechanisms of glial development , 2004, Current Opinion in Neurobiology.

[5]  S. Reed,et al.  Ratchets and clocks: the cell cycle, ubiquitylation and protein turnover , 2003, Nature Reviews Molecular Cell Biology.

[6]  T. Suda,et al.  Defective smooth muscle development in qkI‐deficient mice , 2003, Development, growth & differentiation.

[7]  G. Almazan,et al.  Inhibition of p38 mitogen-activated protein kinase interferes with cell shape changes and gene expression associated with Schwann cell myelination , 2003, Experimental Neurology.

[8]  L. Hengst,et al.  Cell cycle-dependent translation of p27 involves a responsive element in its 5'-UTR that overlaps with a uORF. , 2003, Human molecular genetics.

[9]  M. Greenberg,et al.  Basic Helix-Loop-Helix Factors in Cortical Development , 2003, Neuron.

[10]  Yue Feng,et al.  Tyrosine phosphorylation of QKI mediates developmental signals to regulate mRNA metabolism , 2003, The EMBO journal.

[11]  P. Casaccia‐Bonnefil,et al.  Relationship between cell cycle molecules and onset of oligodendrocyte differentiation , 2003, Journal of neuroscience research.

[12]  P. Jin,et al.  New insights into fragile X syndrome: from molecules to neurobehaviors. , 2003, Trends in biochemical sciences.

[13]  S. Richard,et al.  Nuclear Retention of MBP mRNAs in the Quaking Viable Mice , 2002, Neuron.

[14]  M. Raff,et al.  Posttranscriptional regulation of p18 and p27 Cdk inhibitor proteins and the timing of oligodendrocyte differentiation. , 2002, Developmental biology.

[15]  N. Perrone-Bizzozero,et al.  Role of HuD and other RNA‐binding proteins in neural development and plasticity , 2002, Journal of neuroscience research.

[16]  H. Okano,et al.  Musashi: a translational regulator of cell fate. , 2002, Journal of cell science.

[17]  C. Cepko,et al.  Ectopic expression of Olig1 promotes oligodendrocyte formation and reduces neuronal survival in developing mouse cortex , 2001, Nature Neuroscience.

[18]  T. Schedl,et al.  Identification of in vivo mRNA targets of GLD-1, a maxi-KH motif containing protein required for C. elegans germ cell development. , 2001, Genes & development.

[19]  C. Cepko,et al.  p27Kip1 and p57Kip2 Regulate Proliferation in Distinct Retinal Progenitor Cell Populations , 2001, The Journal of Neuroscience.

[20]  C. Cepko,et al.  Regulating proliferation during retinal development , 2001, Nature Reviews Neuroscience.

[21]  I. Duncan,et al.  Cytoskeletal Reorganization during the Formation of Oligodendrocyte Processes and Branches , 2001, Molecular and Cellular Neuroscience.

[22]  Yue Feng,et al.  Distinct molecular mechanisms lead to diminished myelin basic protein and 2′,3′‐cyclic nucleotide 3′‐phosphodiesterase in qkv dysmyelination , 2001, Journal of neurochemistry.

[23]  S. Richard,et al.  Nuclear translocation controlled by alternatively spliced isoforms inactivates the QUAKING apoptotic inducer. , 2001, Genes & development.

[24]  G. Fishell,et al.  Sonic hedgehog contributes to oligodendrocyte specification in the mammalian forebrain. , 2001, Development.

[25]  Yue Feng,et al.  Destabilization and Mislocalization of Myelin Basic Protein mRNAs in quaking Dysmyelination Lacking the QKI RNA-Binding Proteins , 2000, The Journal of Neuroscience.

[26]  K. Artzt,et al.  The STAR protein QKI-6 is a translational repressor. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[27]  Daniel H. Turnbull,et al.  A method for rapid gain-of-function studies in the mouse embryonic nervoussystem , 1999, Nature Neuroscience.

[28]  James M. Roberts,et al.  CDK inhibitors: positive and negative regulators of G1-phase progression. , 1999, Genes & development.

[29]  J. Keene,et al.  ELAV tumor antigen, Hel-N1, increases translation of neurofilament M mRNA and induces formation of neurites in human teratocarcinoma cells. , 1999, Genes & development.

[30]  E. B. Goodwin,et al.  The STAR protein, GLD‐1, is a translational regulator of sexual identity in Caenorhabditis elegans , 1999, The EMBO journal.

[31]  Natalie A. Lissy,et al.  Transduction of full-length TAT fusion proteins into mammalian cells: TAT-p27Kip1 induces cell migration , 1998, Nature Medicine.

[32]  R. Hardy QKI expression is regulated during neuron‐glial cell fate decisions , 1998, Journal of neuroscience research.

[33]  P. Seth,et al.  Ectopic expression of p27Kip1 in oligodendrocyte progenitor cells results in cell-cycle growth arrest. , 1998, Journal of neurobiology.

[34]  S. Richard,et al.  Structure-Function Analysis of Qk1: a Lethal Point Mutation in Mouse quaking Prevents Homodimerization , 1998, Molecular and Cellular Biology.

[35]  C. Cepko,et al.  Lineage analysis using retroviral vectors. , 1998, Current topics in developmental biology.

[36]  K. Artzt,et al.  STAR, a gene family involved in signal transduction and activation of RNA. , 1997, Trends in genetics : TIG.

[37]  W. K. Miskimins,et al.  Cyclin‐dependent kinase inhibitor P27kip1 is expressed at high levels in cells that express a myelinating phenotype , 1997, Journal of neuroscience research.

[38]  H. Kiyokawa,et al.  Oligodendrocyte precursor differentiation is perturbed in the absence of the cyclin-dependent kinase inhibitor p27Kip1. , 1997, Genes & development.

[39]  M. Raff,et al.  Accumulation of the cyclin‐dependent kinase inhibitor p27/Kip1 and the timing of oligodendrocyte differentiation , 1997, The EMBO journal.

[40]  K. Artzt,et al.  Neural Cell Type-Specific Expression of QKI Proteins Is Altered in quakingviable Mutant Mice , 1996, The Journal of Neuroscience.

[41]  L. Tsai,et al.  The brain-specific activator p35 allows Cdk5 to escape inhibition by p27Kip1 in neurons. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[42]  M. Justice,et al.  The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins , 1996, Nature Genetics.

[43]  G. Almazan,et al.  Phosphorylation and disruption of intermediate filament proteins in oligodendrocyte precursor cultures treated with calyculin A , 1993, Journal of neuroscience research.

[44]  B. Trapp,et al.  Immunocytochemical studies of quaking mice support a role for the myelin-associated glycoprotein in forming and maintaining the periaxonal space and periaxonal cytoplasmic collar of myelinating Schwann cells , 1984, The Journal of cell biology.

[45]  R. Sidman,et al.  Mutant Mice (Quaking and Jimpy) with Deficient Myelination in the Central Nervous System , 1964, Science.

[46]  R. Darnell Paraneoplastic neurologic disorders: windows into neuronal function and tumor immunity. , 2004, Archives of neurology.

[47]  E. Hogan,et al.  Animal Models of Genetic Disorders of Myelin , 1984 .