Use of short hairpin RNA expression vectors to study mammalian neural development

Jenn Yah Yu, Tsu Wei Wang, Anne B. Vojtek, Jack M. Parent, David L. Turner

研究成果: 雜誌貢獻文章

15 引文 (Scopus)

摘要

The use of RNA interference (RNAi) in mammalian cells has become a powerful tool for the analysis of gene function. Here we discuss the use of DNA vectors to produce short hairpin RNAs (shRNAs) and inhibit gene expression in mammalian neural progenitors and neurons. Protocols are presented for introducing shRNA vectors into mouse P19 cells differentiated as neurons in vitro and for electroporation of shRNA vectors into primary neural progenitors from the embryonic mouse dorsal telencephalon (prospective cerebral cortex). Transfected primary cortical progenitors can be differentiated in vitro either in dissociated culture or organotypic slice culture. The use of shRNA vectors for RNAi provides a versatile approach to understand gene function during mammalian neural development.

原文英語
頁(從 - 到)186-199
頁數14
期刊Methods in Enzymology
392
DOIs
出版狀態已發佈 - 2005 一月 24

指紋

Small Interfering RNA
RNA Interference
Neurons
Genes
RNA
Telencephalon
Electroporation
Gene expression
Cerebral Cortex
Cells
Gene Expression
DNA
In Vitro Techniques

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology

引用此文

Use of short hairpin RNA expression vectors to study mammalian neural development. / Yu, Jenn Yah; Wang, Tsu Wei; Vojtek, Anne B.; Parent, Jack M.; Turner, David L.

於: Methods in Enzymology, 卷 392, 24.01.2005, p. 186-199.

研究成果: 雜誌貢獻文章

Yu, Jenn Yah ; Wang, Tsu Wei ; Vojtek, Anne B. ; Parent, Jack M. ; Turner, David L. / Use of short hairpin RNA expression vectors to study mammalian neural development. 於: Methods in Enzymology. 2005 ; 卷 392. 頁 186-199.
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