Characterization of the Role of Macoilin in Dugesia japonica

Loading...
Thumbnail Image

Persistent link to this item

Statistics
View Statistics

Journal Title

Journal ISSN

Volume Title

Title

Characterization of the Role of Macoilin in Dugesia japonica

Published Date

2016-01

Publisher

Type

Thesis or Dissertation

Abstract

Praziquantel, the anti-schistosomiasis drug, is known to induce the bipolar (2-head) phenotypes in regenerative planarian flatworm Dugesia japonica, yet actual mechanism behind this head-instead-of-tail phenotype remains unclear. Previous studies has shown a specific voltage-gated calcium channel subtype, Cav1B, potentiates the bipolar phenotypes among regenerative planarians induced by praziquantel. Here I identify a new transmembrane protein, macoilin, in planarian that has the identical effects to that of Cav1B by RNAi methods. I have shown that by inhibiting the mRNA of macoilin, the regenerative worm under the exposure of praziquantel has a significant increase of bipolar phenotype penetrance compared to the naïve worms. Experimental data has also shown that the macoilin RNAi worms acquire defects in motility after regeneration. These results indicate a possible protein (macoilin) involved in praziquantel-induced signaling pathway that may bring light to the future studies of the mechanism of praziquantel.

Description

University of Minnesota M.S. thesis. January 2016. Major: Pharmacology. Advisor: Jonathan Marchant. 1 computer file (PDF); vi, 35 pages.

Related to

Replaces

License

Series/Report Number

Funding information

Isbn identifier

Doi identifier

Previously Published Citation

Suggested citation

Ren, Ruodi. (2016). Characterization of the Role of Macoilin in Dugesia japonica. Retrieved from the University Digital Conservancy, https://hdl.handle.net/11299/178919.

Content distributed via the University Digital Conservancy may be subject to additional license and use restrictions applied by the depositor. By using these files, users agree to the Terms of Use. Materials in the UDC may contain content that is disturbing and/or harmful. For more information, please see our statement on harmful content in digital repositories.