9 research outputs found

    Isolation and Characterization of Two Novel, Cytoplasmically Polyadenylated, Oocyte-Specific, Mouse Maternal RNAs

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    AbstractDuring early development in mouse andXenopus,translational activation of stored maternal mRNAs by cytoplasmic polyadenylation requires both the nuclear polyadenylation signal AAUAAA and U-richcis-acting adenylation control elements (ACEs), also termed cytoplasmic polyadenylation elements, located in the 3′ UTR. Using an ACE-based PCR strategy (Salléset al.,1992) we have isolated two novel cDNAs from mouse oocytes: OM2a and OM2b (for Oocyte Maturation). Each message contains an ACE consensus sequence upstream of AAUAAA, is specifically transcribed in the growing oocyte, and is cytoplasmically polyadenylated upon oocyte maturation. Comparison of the mouse and rat homologs reveals considerable nucleotide sequence homology and conservation of overall gene organization. However, the predicted open reading frames are far less conserved, suggesting that these genes may not be functioning as proteins. The tissue specificity and tight temporal regulation of the RNAs suggest a role for these genes during early development

    72nd Congress of the Italian Society of Pediatrics

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    Dissociation of mRNA cytoplasmic polyadenylation from translational activation by structural modification of the 5’-UTR

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    Evolutionary conservation of sequence elements controlling cytoplasmic polyadenylylation

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    Nanos and pumilio establish embryonic polarity in Drosophila by promoting posterior deadenylation of hunchback mRNA

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    Role of glycine-82 as a pivot point during the transition from the inactive to the active form of the yeast Ras2 protein

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    RAS residues that are distant from the GDP binding site play a critical role in dissociation factor-stimulated release of GDP

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