Deep sequencing identifies new and regulated microRNAs in Schmidtea mediterranea (original) (raw)
- Yi-Chien Lu1,
- Magda Smielewska1,
- Dasaradhi Palakodeti1,
- Michael T. Lovci2,
- Stefan Aigner3,
- Gene W. Yeo2 and
- Brenton R. Graveley1
- 1Department of Genetics and Developmental Biology, University of Connecticut Stem Cell Institute, University of Connecticut Health Center, Farmington, Connecticut 06030-3301, USA
- 2Department of Cellular and Molecular Medicine, Stem Cell Program, UCSD Moores Cancer Center, University of California, San Diego, La Jolla, California 92037, USA
- 3Laboratory of Genetics, Salk Institute, La Jolla, California 92037, USA
Abstract
MicroRNAs (miRNAs) play important roles in directing the differentiation of cells down a variety of cell lineage pathways. The planarian Schmidtea mediterranea can regenerate all lost body tissue after amputation due to a population of pluripotent somatic stem cells called neoblasts, and is therefore an excellent model organism to study the roles of miRNAs in stem cell function. Here, we use a combination of deep sequencing and bioinformatics to discover 66 new miRNAs in S. mediterranea. We also identify 21 miRNAs that are specifically expressed in either sexual or asexual animals. Finally, we identified five miRNAs whose expression is sensitive to γ-irradiation, suggesting they are expressed in neoblasts or early neoblast progeny. Together, these results increase the known repertoire of S. mediterranea miRNAs and identify numerous regulated miRNAs that may play important roles in regeneration, homeostasis, neoblast function, and reproduction.
Footnotes
Reprint requests to: Brenton R. Graveley, Department of Genetics and Developmental Biology, University of Connecticut Stem Cell Institute, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030-3301, USA; e-mail: graveley{at}neuron.uchc.edu; fax: (860) 679-8345; or Gene W. Yeo, Department of Cellular and Molecular Medicine, Stem Cell Program, UCSD Moores Cancer Center, University of California, San Diego, 9500 Gilman Drive, MC0695, La Jolla, CA 92037, USA; e-mail:geneyeo{at}ucsd.edu, fax: (858) 822-3249.
Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.1702009.
- Received April 23, 2009.
- Accepted April 29, 2009.
Copyright © 2009 RNA Society
