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

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)186-199
Number of pages14
JournalMethods in Enzymology
Volume392
DOIs
Publication statusPublished - 2005 Jan 24

Fingerprint

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

Cite this

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.

In: Methods in Enzymology, Vol. 392, 24.01.2005, p. 186-199.

Research output: Contribution to journalArticle

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. In: Methods in Enzymology. 2005 ; Vol. 392. pp. 186-199.
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