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In vivo visualization of alternative splicing

01.28.08 | Cold Spring Harbor Laboratory

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The February 1 cover of G&D features an unprecedented use of fluorescent proteins to visualize developmentally regulated alternative mRNA splicing in a living organism. Dr. Hidehito Kuroyanagi and colleagues at the Tokyo Medical and Dental University engineered a transgenic alternative splicing reporter system to monitor the developmentally regulated switching of let-2 alternative splicing in live C. elegans worms. The splicing of let-2 changes during the lifetime of the worm: Embryos and early larvae express exon 9, while adult worms express exon 10. By linking exons 9 and 10 with differently colored fluorescent proteins (green and red, respectively).

Drs. Kuroyanagi & Hagiwara's team was able to visually monitor let-2 splicing patterns during the life of an individual worm. “The reporter system enables experimental analysis of regulation mechanisms underlying the developmental or cell-type-specific profiles of alternative splicing in living organisms. We are coming to realize that the molecular mechanisms of alternative splicing are highly conserved throughout metazoan evolution,” explains Dr. Kuroyanagi.

Genes & Development

Keywords

Article Information

Contact Information

Heather Cosel
coselpie@cshl.edu

How to Cite This Article

APA:
Cold Spring Harbor Laboratory. (2008, January 28). In vivo visualization of alternative splicing. Brightsurf News. https://www.brightsurf.com/news/1GN3ZRXL/in-vivo-visualization-of-alternative-splicing.html
MLA:
"In vivo visualization of alternative splicing." Brightsurf News, Jan. 28 2008, https://www.brightsurf.com/news/1GN3ZRXL/in-vivo-visualization-of-alternative-splicing.html.