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  Sequence and expression differences underlie functional specialization of Arabidopsis microRNAs miR159 and miR319

Palatnik, J., Wollmann, H., Schommer, C., Schwab, R., Boisbouvier, J., Rodriguez, R., et al. (2007). Sequence and expression differences underlie functional specialization of Arabidopsis microRNAs miR159 and miR319. Developmental Cell, 13(1), 115-125. doi:10.1016/j.devcel.2007.04.012.

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Palatnik, JF1, Autor           
Wollmann, H1, Autor           
Schommer, C1, Autor           
Schwab, R1, Autor           
Boisbouvier, J, Autor
Rodriguez, R, Autor
Warthmann, N1, Autor           
Allen, E, Autor
Dezulian, T, Autor
Huson, D, Autor           
Carrington , JC, Autor
Weigel, D1, Autor           
Affiliations:
1Department Molecular Biology, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3375790              

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 Zusammenfassung: Many microRNAs (miRNAs) are encoded by small gene families. In a third of all conserved Arabidopsis miRNA families, members vary at two or more nucleotide positions. We have focused on the related miR159 and miR319 families, which share sequence identity at 17 of 21 nucleotides, yet affect different developmental processes through distinct targets. MiR159 regulates MYB mRNAs, while miR319 predominantly acts on TCP mRNAs. In the case of miR319, MYB targeting plays at most a minor role because miR319 expression levels and domain limit its ability to affect MYB mRNAs. In contrast, in the case of miR159, the miRNA sequence prevents effective TCP targeting. We complement these observations by identifying nucleotide positions relevant for miRNA activity with mutants recovered from a suppressor screen. Together, our findings reveal that functional specialization of miR159 and miR319 is achieved through both expression and sequence differences.

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 Datum: 2007-07
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: -
 Identifikatoren: DOI: 10.1016/j.devcel.2007.04.012
PMID: 17609114
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Titel: Developmental Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 13 (1) Artikelnummer: - Start- / Endseite: 115 - 125 Identifikator: ISSN: 1534-5807
CoNE: https://pure.mpg.de/cone/journals/resource/111006902714134