The Orphan Nuclear Receptor TLX/NR2E1 in Neural Stem Cells and Diseases

The human TLX gene encodes an orphan nuclear receptor predominantly expressed in the central nervous system. Tailess and Tlx, the TLX homologues in Drosophila and mouse, play essential roles in body-pattern formation and neurogenesis during early embryogenesis and perform crucial functions in mainta...

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Published in:Neuroscience bulletin Vol. 32; no. 1; pp. 108 - 114
Main Authors: Wang, Tao, Xiong, Jian-Qiong
Format: Journal Article
Language:English
Published: Singapore Springer Singapore 01-02-2016
Springer
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Summary:The human TLX gene encodes an orphan nuclear receptor predominantly expressed in the central nervous system. Tailess and Tlx, the TLX homologues in Drosophila and mouse, play essential roles in body-pattern formation and neurogenesis during early embryogenesis and perform crucial functions in maintaining stemness and controlling the differentiation of adult neural stem cells in the central nervous system, especially the visual system. Multiple target genes and signaling pathways are regulated by TLX and its homologues in specific tissues during various developmental stages. This review aims to sum- marize previous studies including many recent updates from different aspects concerning TLX and its homologues in Drosophila and mouse.
Bibliography:31-1975/R
TLX ; Neural stem cell ; Neurogenesis
The human TLX gene encodes an orphan nuclear receptor predominantly expressed in the central nervous system. Tailess and Tlx, the TLX homologues in Drosophila and mouse, play essential roles in body-pattern formation and neurogenesis during early embryogenesis and perform crucial functions in maintaining stemness and controlling the differentiation of adult neural stem cells in the central nervous system, especially the visual system. Multiple target genes and signaling pathways are regulated by TLX and its homologues in specific tissues during various developmental stages. This review aims to sum- marize previous studies including many recent updates from different aspects concerning TLX and its homologues in Drosophila and mouse.
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ISSN:1673-7067
1995-8218
DOI:10.1007/s12264-015-0004-7