Nuclear processing and export of microRNAs in Arabidopsis.

By M. Park, Gang Wu, Alfredo Gonzalez-Sulser, H. Vaucheret, R. Poethig. Proceedings of the National Academy of Sciences of the United States of America, 2005

705 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/03275bba28334eac9f8fd78cb9d0c6783638a59d

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Citations in the corpus

Molecular mechanisms of flower development: an armchair guide (2005, background): “Mutations in these genes affect the expression of a number of targets, including AG (Ref”
microRNA-directed phasing during trans-acting siRNA biogenesis in plants. (2005, background): “…miRNA-defective dcl1-7, hen1-1, and hyl1-2 (Park et al., 2002; Schauer et al., 2002; Vazquez et al., 2004a), which were shown to reduce or eliminate accumulation of miRNAs, and a new insertion mutant, hst15, with defects in nucleocytoplasmic transport of miRNA precursors (Park et al., 2005).”
MicroRNA biogenesis: coordinated cropping and dicing (2005, background): “A recent study showed that loss-of-function mutants in HST reduced the accumulation of most miRNAs, indicating that HST functions as a nuclear export recepto”
Plant microRNA: a small regulatory molecule with big impact. (2006, background): “, 2003; Bartel, 2004), then the duplex is translocated into the cytoplasm by HASTY, the plant orthologue of exportin 5 (Park et al., 2005).”
The control of developmental phase transitions in plants (2011, background): “Experimental evidence that the miRNA recognition elements (MREs) of these transcripts are indeed responsive and functional is diverse and convincing (Franco-Zorrilla et al., 2007; Martin et al., 2010b; Park et al., 2005; Schwab et al., 2005; Shikata et al., 2009; Usami et al., 2009; Wang et al., 200”
Functions of microRNAs and related small RNAs in plants (2006, background): “thaliana mutant impaired in the ortholog of Exp-5, but it is unknown whether miRNA duplexes or mature miRNAs are exported by HASTY to the cytoplas”
Temporal regulation of shoot development in Arabidopsis thaliana by miR156 and its target SPL3 (2006, background): “We chose hst-6 because this mutation specifically affects miRNAs, produces a significant decrease in miR156 (Park et al., 2005) and has a precocious vegetative phenotype (Telfer and Poethig, 1998).”
Biogenesis, Turnover, and Mode of Action of Plant MicroRNAs[OPEN] (2013, background): “of miRNAs is unchanged in hst mutants (Park et al., 2005).”
MicroRNAS and their regulatory roles in plants. (2006, background): “None of the other three Dicerlike enzymes in Arabidopsis is required for miRNA biogenesis (41, 142), suggesting that DCL1 also makes the second set of cuts.”
microPrimer: the biogenesis and function of microRNA (2005, background): “The resulting miRNA/miRNA* duplex is exported from the nucleus by HASTY (HST), the plant ortholog of Exportin 5, and completes its assembly into the RISC in the cytoplasm (Peragine et al., 2004; Park et al., 2005).”
Origin, biogenesis, and activity of plant microRNAs. (2009, neutral): “hasty mutants show decreased accumulation of only some miRNAs, in both nuclear and cytoplasmic fractions (Park et al., 2005), suggesting the existence of HASTY-independent miRNA export systems.”
The timing of developmental transitions in plants. (2006, background): “HST encodes a homolog of the mammalian exportin5 nuclear export receptor and is thought to export miRNA into the cytoplasm (Park et al., 2005).”
Cooperative Regulation of Flavonoid and Lignin Biosynthesis in Plants (2021, background): “Since the first plant MYB gene was isolated (Paz-Ares et al., 1987), research concerning the identification and functional characterization of the MYB gene family has been conducted in plants with the help of available plant genome sequences in various databases (Jiang and Rao, 2020).”