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  Heterologous reporter expression in the planarian Schmidtea mediterranea through somatic mRNA transfection

Hall, R. N., Weill, U., Drees, L., Leal-Ortiz, S., Li, H., Khariton, M., et al. (2022). Heterologous reporter expression in the planarian Schmidtea mediterranea through somatic mRNA transfection. Cell Reports: Methods, 2(10): 100298. doi:10.1016/j.crmeth.2022.100298.

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 Creators:
Hall, Richard Nelson, Author
Weill, Uri1, Author           
Drees, Leonard1, Author           
Leal-Ortiz, Sergio, Author
Li, Hongquan, Author
Khariton, Margarita, Author
Chai, Chew, Author
Xue, Yuan, Author
Rosental, Benyamin, Author
Quake, Stephen R., Author
Alvarado, Alejandro Sánchez, Author
Melosh, Nicholas A., Author
Fire, Andrew Z., Author
Rink, Jochen Christian1, Author           
Wang, Bo, Author
Affiliations:
1Department of Tissue Dynamics and Regeneration, Max Planck Institute for Multidisciplinary Sciences, Max Planck Society, Göttingen, DE, ou_3350274              

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 Abstract: Planarians have long been studied for their regenerative abilities. Moving forward, tools for ectopic expression of non-native proteins will be of substantial value. Using a luminescent reporter to overcome the strong autofluorescence of planarian tissues, we demonstrate heterologous protein expression in planarian cells and live animals. Our approach is based on the introduction of mRNA through several nanotechnological and chemical transfection methods. We improve reporter expression by altering untranslated region (UTR) sequences and codon bias, facilitating the measurement of expression kinetics in both isolated cells and whole planarians using luminescence imaging. We also examine protein expression as a function of variations in the UTRs of delivered mRNA, demonstrating a framework to investigate gene regulation at the post-transcriptional level. Together, these advances expand the toolbox for the mechanistic analysis of planarian biology and establish a foundation for the development and expansion of transgenic techniques in this unique model system.

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Language(s): eng - English
 Dates: 2022-08-252022-09-202022-10-24
 Publication Status: Issued
 Pages: -
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 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.crmeth.2022.100298
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Project name : We thank K. Lei and C. Kuhn for stimulating discussion and E. Liu, D. Burghardt, Y. Lim, and T. Boothe for technical assistance. R.N.H. is supported by an NSF Graduate Research Fellowship. U.W. is supported by an EMBO Long-Term Fellowship. B.W. is a Beckman Young Investigator. U.W., L.D., and J.C.R. are supported by the Max Planck Society. A.Z.F. is supported by an NIH grant (R35GM130366). B.W. and B.R. appreciate the support from an HFSP grant (RGY0085/2019). This work was initiated through a Stanford Bio-X Interdisciplinary Initiative seed grant (IIP9-64) to B.W., A.Z.F., and N.A.M. and later supported by an NSF EDGE grant (IOS-1923534) to B.W., A.S.A., and N.A.M., and a Volkswagen Foundation grant (Az.-99498) to J.C.R. and B.W.
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Title: Cell Reports: Methods
Source Genre: Journal
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Publ. Info: Amsterdam : Elsevier
Pages: - Volume / Issue: 2 (10) Sequence Number: 100298 Start / End Page: - Identifier: Other: ISSN
CoNE: https://pure.mpg.de/cone/journals/resource/2667-2375