Moving messages in the developing brain-emerging roles for mRNA transport and local translation in neural stem cells

被引:20
|
作者
Pilaz, Louis-Jan [1 ]
Silver, Debra L. [1 ,2 ,3 ,4 ]
机构
[1] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Regenerat Next, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Duke Inst Brain Sci, Durham, NC USA
来源
FEBS LETTERS | 2017年 / 591卷 / 11期
关键词
neurogenesis; RNA localization; translation; RADIAL GLIAL-CELLS; FRAGILE-X-SYNDROME; BASEMENT-MEMBRANE INTEGRITY; DEVELOPING CEREBRAL-CORTEX; OUTER SUBVENTRICULAR ZONE; CYCLIN-DEPENDENT KINASES; BINDING-PROTEIN STAUFEN2; PROGENITOR CELLS; IN-VIVO; MAMMALIAN NEUROGENESIS;
D O I
10.1002/1873-3468.12626
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian cerebral cortex is a complex brain structure integral to our higher cognition. During embryonic cortical development, radial glial progenitors (RGCs) produce neurons and serve as physical structures for migrating neurons. Recent discoveries highlight new roles for RNA localization and local translation in RGCs, both at the cell body and at distal structures called basal endfeet. By implementing technologies from the field of RNA research to brain development, investigators can manipulate RNA-binding proteins as well as visualize single-molecule RNAs, live movement of mRNAs and their binding proteins, and translation. Going forward, these studies establish a framework for investigating how post-transcriptional RNA regulation helps shape RGC function and triggers neurodevelopmental diseases.
引用
收藏
页码:1526 / 1539
页数:14
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