MicroRNA-dependent localization of targeted mRNAs to mammalian P-bodies
By Jidong Liu, M. A. Valencia-Sanchez, Gregory J. Hannon, R. Parker. Nature Cell Biology, 2005
1,341 citations recorded by the source corpus.
Subfields: Cancer Research, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/787de4c8a5558ddca3a024bbb8025bf0a43a04bd
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In Cancer Research
- David P. Bartel
- Xuemei Chen
- M. Jones-Rhoades
- Phillip D. Zamore
- Alexander Stark
- David Baltimore
- W. Filipowicz
- D. Rao
In Molecular Biology
- David P. Bartel
- Xuemei Chen
- Jian‐Kang Zhu
- Phillip D. Zamore
- R. Parker
- Elisa Izaurralde
- Gregory J. Hannon
- W. Filipowicz
Citations in the corpus
- RNA silencing: Methods and protocols (2006, positive): “Specific circulating miRNA profiles have previously been described in patients with chronic heart failure (CHF).[5-9] A few studies have examined miRNAs in acute heart failure (AHF).”
- P-Body Formation Is a Consequence, Not the Cause, of RNA-Mediated Gene Silencing (2007, background): “... mRNA decay (NMD), a pathway that degrades mRNAs harboring premature translation termination codons (or nonsense codons) (22, 45, 52); (ii) proteins with roles in AU-rich element (ARE)mediated mRNA decay, a pathway that degrades mRNAs containing AU-rich elements in their 3 untranslated regions (U”
- Many roads to maturity: microRNA biogenesis pathways and their regulation (2009, background): “P-bodies are sites of accumulation of untranslated mRNAs and of multiple enzymes involved in mRNA turnover and translational repression, including Ago proteins and miRNA”
- MicroRNAS and their regulatory roles in plants. (2006, background): “This suggests that miRNA binding directs the message to the P body, where it can be sequestered from the translation machinery and destabilized (77, 120).”
- General translational repression by activators of mRNA decapping. (2005, background): “ore recently, the demonstration that mRNAs translaionally repressed by miRNAs accumulate in P bodies uggests that miRNA based translational repression ight also interact with this general translation represion machinery (Liu et al., 2005).”
- A role for the P-body component GW182 in microRNA function (2005, background): “Recently, Argonaute proteins, which are key RNAi effector components, and their target mRNAs were shown to localize to cytoplasmic foci known as P-bodies or GW-bodie”
- Biogenesis, Turnover, and Mode of Action of Plant MicroRNAs[OPEN] (2013, background): “…Processing Body Processing (P)-bodies are cytoplasmic ribonucleoprotein aggregates where translationally repressed mRNAs, including miRNA targets, accumulate (Teixeira et al., 2005; Liu et al., 2005), prior to either degradation or reinitiation of translation (reviewed in Eulalio et al., 2007a).”
- How do microRNAs regulate gene expression? (2008, background): “The interactions with Dcp1/2 and GW182 still occurred with Ago mutants deficient in RNA binding that did not localize to P-bodies ( 54 , 67), and the interaction with p54 still occurred in cells depleted of Lsm1 (a protein found in P-bodies and implicated in RNA processing), which dispersed the foci”