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Journal Article

New microRNAs from mouse and human

MPS-Authors

Lagos-Quintana,  M.
Max Planck Society;

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Rauhut,  R.
Department of Cellular Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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Meyer,  J.
Research Group of Combinatorical Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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Tuschl,  T.
Research Group of Combinatorical Biochemistry, MPI for biophysical chemistry, Max Planck Society;

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641886.pdf
(Publisher version), 181KB

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Citation

Lagos-Quintana, M., Rauhut, R., Meyer, J., Borkhardt, A., & Tuschl, T. (2003). New microRNAs from mouse and human. RNA, 9(2), 175-179. Retrieved from http://rnajournal.cshlp.org/content/9/2/175.full.pdf+html.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-94EA-2
Abstract
MicroRNAs (miRNAs) represent a new class of noncoding RNAs encoded in the genomes of plants, invertebrates, and vertebrates. MicroRNAs regulate translation and stability of target mRNAs based on (partial) sequence complementarity. Although the number of newly identified miRNAs is still increasing, target mRNAs of animal miRNAs remain to be identified. Here we describe 31 novel miRNAs that were identified by cloning from mouse tissues and the human Saos-2 cell line. Fifty-three percent of all known mouse and human miRNAs have homologs in Fugu rubripes (pufferfish) or Danio rerio (zebrafish), of which almost half also have a homolog in Caenorhabditis elegans or Drosophila melanogaster. Because of the recurring identification of already known miRNAs and the unavoidable background of ribosomal RNA breakdown products, it is believed that not many more miRNAs may be identified by cloning. A comprehensive collection of miRNAs is important for assisting bioinformatics target mRNA identification and comprehensive genome annotation.