Translational control by CPEB: a means to the end

By R. Méndez, Joel D. Richter. Nature reviews. Molecular cell biology, 2001

646 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/72c236ae946a70b8b1c4c3ace767ea9ffbff53b3

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

Citations in the corpus

Dendritic mRNA: transport, translation and function (2007, background): “CPEB1-mediated translation is activated when CPEB1 is phosphorylated at two crucial residues (Thr171 and Ser177 in mouse”
Patterns, mechanisms, and functions of translation regulation in mammalian spermatogenic cells (2004, background): “Widely diverse animals from Drosophila to mammals activate translation of mRNAs containing a U-rich cytoplasmic polyadenylation element (CPE) located slightly upstream of the AAUAAA polyadenylation signal during female meiosis, oocyte maturation and early development (Mendez and Richter, 2001).”
Translational regulatory mechanisms in persistent forms of synaptic plasticity. (2004, neutral): “Rapamycin also inhibits polyadenylation (Mendez and Richter, 2001).”
Extensive Association of Functionally and Cytotopically Related mRNAs with Puf Family RNA-Binding Proteins in Yeast (2004, background): “Iron regulatory proteins (IRPs) bind to and regulate translation of five different mRNAs encoding proteins involved in iron metabolism (Eisenstein and Ross 2003), and a cytoplasmic poly(A) polymerase regulates multiple mRNAs in early development (Mendez and Richter 2001).”
Molecular mechanisms of translational control (2004, background): “This protein binds to a uridinerich sequence -the cytoplasmic polyadenylation element (CPE) -that is located in the 3′ UTR of target mRNAs and promotes both silencing of the mRNA before oocyte maturation as well as subsequent cytoplasmic polyadenylation and translational activation 29 .”
The endoplasmic reticulum: structure, function and response to cellular signaling (2015, background): “Given the timing of each of these reorganizations, it seems likely that they are related to increases in cyclinB:cdk1 activity that occurs upon oocyte maturation [136].”
Codon identity regulates mRNA stability and translation efficiency during the maternal‐to‐zygotic transition (2016, neutral): “…with the median indicated with a thick black line and vertical lines indicate the variability outside the upper and lower quartiles. activation, fertilization, or zygotic genome activation, depending on the specific mRNA (Mendez & Richter, 2001; Clark et al, 2007; Yartseva & Giraldez, 2015).”
Human MicroRNA Targets (2004, methodology): “We used a search pattern using four criteria: (1) presence of the CPE motif UUUUAU, (2) presence of the hexanucleotide AAUAAA, (3) the CPE and the hexanucleotide motif being within 100 nucleotides of each other, and (4) the conservation of these motifs and the positions of the motifs in the mouse or”