CARPEL FACTORY, a Dicer homolog, and HEN1, a novel protein, act in microRNA metabolism in Arabidopsis thaliana.

By Wonkeun Park, Junjie Li, R. Song, J. Messing, Xuemei Chen. Current Biology, 2002

1,297 citations recorded by the source corpus.

Subfields: Cancer Research, Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/e727761c3c8a88f9a4c38273713cc57e48218567

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Citations in the corpus

Endogenous siRNAs Derived from a Pair of Natural cis-Antisense Transcripts Regulate Salt Tolerance in Arabidopsis (2005, neutral): “DCL1 is required for the production of 21-nt miRNAs and trans-acting siRNAs (tasiRNAs) (Park et al., 2002; Peragine et al., 2004; Vazquez et al., 2004b).”
MicroRNA targets in Drosophila (2003, neutral): “Both siRNAs and miRNAs are processed from doublestranded RNA precursors requiring dsRNA-specific RNase III enzymes [26-30].”
Computational identification of plant microRNAs and their targets, including a stress-induced miRNA. (2004, background): “…that search for short segmentsexcised by Dicer-like enzymes (Grishok et al., 2001; Hutof conserved complementarity to the miRNAs are re-vagner et al., 2001; Ketting et al., 2001; Lee et al., 2002, quired to identify metazoan miRNA targets (Enright et2003; Park et al., 2002; Reinhart et al., 2002).”
The control of developmental phase transitions in plants (2011, background): “…in A. thaliana; MIR172b=EARLY ACTIVATION TAGGED (EAT) Aukerman and Sakai, 2003 Axtell and Bowman, 2008 Cuperus et al., 2011 Jung et al., 2007 Park et al., 2002 Schwab et al., 2005 Wu et al., 2009 AP2 A. thaliana At4g36920 Repressor of flowering and floral homeotic gene; a founding member of…”
Photoperiodic flowering of Arabidopsis: integrating genetic and physiological approaches to characterization of the floral stimulus (2005, methodology): “Using an activation-tagging approach, Aukerman & Sakai (2003) and Chen (2004) found that miR172 (Park et al. 2002), which is normally expressed in a temporal manner, causes early flowering and disrupts the specification of floral organ identity when overexpressed in Arabidopsis.”
Novel and Mechanical Stress–Responsive MicroRNAs in Populus trichocarpa That Are Absent from Arabidopsisw⃞ (2005, methodology): “Failure to detect the transcripts of cloned or computationally identifiedmiRNAsby RNA gel blotting has been reported in previous studies (Park et al., 2002; Reinhart et al., 2002; Jones-Rhoades and Bartel, 2004; Sunkar and Zhu, 2004; Wang et al., 2004a, 2004b; Adai et al., 2005).”
The action of ARGONAUTE1 in the miRNA pathway and its regulation by the miRNA pathway are crucial for plant development. (2004, background): “3A), suggesting that AGO1 acts downstream from DCL1, HEN1, and HYL1 in the miRNA pathway to promote cleavage of target mRNAs.”
Microarray-based analysis of stress-regulated microRNAs in Arabidopsis thaliana. (2008, background): “With the discovery of large numbers of miRNAs in both plants and animals, the important roles of these special small RNAs have been widely recognized (Llave et al. 2002; Park et al. 2002; Ambros 2004).”
A pathway for the biogenesis of trans-acting siRNAs in Arabidopsis. (2005, background): “DCL1 is required for the biogenesis of miRNAs (Park et al. 2002) but is not required for PTGS of a hairpin transgene (Finnegan et al. 2003).”
The microRNAs of Caenorhabditis elegans. (2003, methodology): “Because gene-prediction programs had not been developed to identify miRNAs in genomic sequence, miRNA gene identification has been primarily achieved by cloning the small RNAs from size-fractionated RNA samples, sometimes specifically enriching in miRNAs by first immunoprecipitating the miRNP comple”
Evolution of microRNA genes by inverted duplication of target gene sequences in Arabidopsis thaliana (2004, background): “; in plants, multiple steps may be catalyzed by Dicer-like1 (DCL1”