Control of leaf morphogenesis by microRNAs

By Javier F. Palatnik, Edwards Allen, Xuelin Wu, C. Schommer, R. Schwab, James C. Carrington, Detlef Weigel. Nature, 2003

1,789 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/dcff85288cdc805bf30b9b9014b8c6db790c5c34

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Citations in the corpus

Highly Specific Gene Silencing by Artificial MicroRNAs in Arabidopsis[W][OA] (2006, background): “Second, because miRNA-insensitive variants can be generated that do not differ in the encoded protein sequence of targets (Palatnik et al., 2003), mutant defects of amiRNAexpressing plants can be complemented, which is not easily possible with RNAi plants.”
The miRNA156/157 recognition element in the 3' UTR of the Arabidopsis SBP box gene SPL3 prevents early flowering by translational inhibition in seedlings. (2007, background): “In addition, expression arrays have been used to show target level reduction in response to miRNA expression (Palatnik et al., 2003; Schwab et al., 2005).”
Viral RNA silencing suppressors inhibit the microRNA pathway at an intermediate step. (2004, background): “In plants, miRNAs target a wide range of mRNAs encoding transcription factors required for development (Park et al. 2002; Rhoades et al. 2002; Palatnik et al. 2003).”
A CRISPR/Cas9 Toolbox for Multiplexed Plant Genome Editing and Transcriptional Regulation1[OPEN] (2015, background): “Vol. 169, 2015 Borevitz et al., 2000) and miR319 (a microRNA; Weigel et al., 2000; Palatnik et al., 2003).”
Computational prediction of miRNAs in Arabidopsis thaliana. (2005, background): “The mRNA transcript sequences that may be targets of these miRNAs have previously been suggested (Rhoades et al. 2002; Palatnik et al. 2003) and some confirmed experimentally (Llave et al.”
Human embryonic stem cells express a unique set of microRNAs. (2004, background): “In plants, miRNAs show a high degree of complementarity to transcription factors that are significant in development (Aukerman and Sakai, 2003; Chen, 2003; Llave et al., 2002b; Palatnik et al., 2003; Rhoades et al., 2002).”
The Balance between the MIR164A and CUC2 Genes Controls Leaf Margin Serration in Arabidopsis[W] (2006, background): “A similar leaf phenotype is observed in Arabidopsis plants overexpressing miR-JAW, a microRNA (miRNA) targeting several transcripts of the TCP family of transcription factors related to CIN in Antirrhinum (Palatnik et al., 2003).”
Post-transcriptional small RNA pathways in plants: mechanisms and regulations. (2006, background): “GENES & DEVELOPMENT 765 to cell via plasmodesmata and at long distance through the vascular tissues (Palauqui et al. 1997; Voinnet et al. 1998).”
Plant microRNA: a small regulatory molecule with big impact. (2006, background): “Overexpression of miRJAW resulted in low levels of all tested TCP mRNAs and caused jaw-D phenotypes, including uneven leaf shape and curvature (Palatnik et al., 2003).”
Differentially Expressed miRNAs Potentially Involved in the Regulation of Defense Mechanism to Drought Stress in Maize Seedlings (2009, methodology): “The content of hormone ABA was measured by indirect enzyme-linked immunosorbent assay (ELISA; Ross et al. 1987).”
Role of miRNAs and siRNAs in biotic and abiotic stress responses of plants (2011, neutral): “In related studies, increased or decreased levels of ARF10 altered GH3-like gene expression and led to severe developmental defects, miR160-resistant ARF plants were found to have dramatic developmental abnormalities, and ARF10 was found to regulate floral organ identity and to be involved in seed g”
Conservation and divergence of plant microRNA genes. (2006, background): “miR-JAW mutants caused uneven leaf shape and leaf curvature in Arabidopsis thaliana and in maize by decreasing a subset of TCP (TBI, CYC, PCF) gene expression (Llave et al., 2002; Palatnik et al., 2003).”