Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2

被引:139
作者
Meijer, Dimphna H. [1 ,2 ]
Kane, Michael F. [1 ,2 ]
Mehta, Shwetal [1 ,2 ]
Liu, Hongye [3 ]
Harrington, Emily [4 ,5 ]
Taylor, Christopher M. [1 ,2 ,6 ]
Stiles, Charles D. [1 ,2 ]
Rowitch, David H. [4 ,5 ]
机构
[1] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02215 USA
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA
[3] Childrens Hosp, Informat Program, Boston, MA 02115 USA
[4] Univ Calif San Francisco, Dept Pediat, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Neurol Surg, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[6] EMD Serono Res Inst, Billerica, MA 01821 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR OLIG2; NEURAL STEM-CELLS; OLIGODENDROCYTE PRECURSORS; PROGENITOR CELLS; BRAIN-INJURY; SPINAL-CORD; SUBVENTRICULAR ZONE; GENE-EXPRESSION; NUCLEAR EXPORT; BHLH PROTEINS;
D O I
10.1038/nrn3386
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The basic helix-loop-helix transcription factors oligodendrocyte transcription factor 1 (OLIG1) and OLIG2 are structurally similar and, to a first approximation, coordinately expressed in the developing CNS and postnatal brain. Despite these similarities, it was apparent from early on after their discovery that OLIG1 and OLIG2 have non-overlapping developmental functions in patterning, neuron subtype specification and the formation of oligodendrocytes. Here, we summarize more recent insights into the separate roles of these transcription factors in the postnatal brain during repair processes and in neurological disease states, including multiple sclerosis and malignant glioma. We discuss how the unique functions of OLIG1 and OLIG2 may reflect their distinct genetic targets, co-regulator proteins and/or post-translational modifications.
引用
收藏
页码:819 / 831
页数:13
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