<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(22)</volume><submitter>Semotok JL</submitter><pubmed_abstract>SMAUG (SMG) is an RNA-binding protein that functions as a key component of a transcript degradation pathway that eliminates maternal mRNAs in the bulk cytoplasm of activated Drosophila melanogaster eggs. We previously showed that SMG destabilizes maternal Hsp83 mRNA by recruiting the CCR4-NOT deadenylase to trigger decay; however, the cis-acting elements through which this was accomplished were unknown. Here we show that Hsp83 transcript degradation is regulated by a major element, the Hsp83 mRNA instability element (HIE), which maps to a 615-nucleotide region of the open reading frame (ORF). The HIE is sufficient for association of a transgenic mRNA with SMG protein as well as for SMG-dependent destabilization. Although the Hsp83 mRNA is translated in the early embryo, we show that transl</pubmed_abstract><journal>Molecular and cellular biology</journal><pagination>6757-72</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2573300</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Drosophila maternal Hsp83 mRNA destabilization is directed by multiple SMAUG recognition elements in the open reading frame.</pubmed_title><pmcid>PMC2573300</pmcid><pubmed_authors>Semotok JL</pubmed_authors><pubmed_authors>Cooperstock RL</pubmed_authors><pubmed_authors>Vari HK</pubmed_authors><pubmed_authors>Luo H</pubmed_authors><pubmed_authors>Smibert CA</pubmed_authors><pubmed_authors>Karaiskakis A</pubmed_authors><pubmed_authors>Lipshitz HD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Drosophila maternal Hsp83 mRNA destabilization is directed by multiple SMAUG recognition elements in the open reading frame.</name><description>SMAUG (SMG) is an RNA-binding protein that functions as a key component of a transcript degradation pathway that eliminates maternal mRNAs in the bulk cytoplasm of activated Drosophila melanogaster eggs. We previously showed that SMG destabilizes maternal Hsp83 mRNA by recruiting the CCR4-NOT deadenylase to trigger decay; however, the cis-acting elements through which this was accomplished were unknown. Here we show that Hsp83 transcript degradation is regulated by a major element, the Hsp83 mRNA instability element (HIE), which maps to a 615-nucleotide region of the open reading frame (ORF). The HIE is sufficient for association of a transgenic mRNA with SMG protein as well as for SMG-dependent destabilization. Although the Hsp83 mRNA is translated in the early embryo, we show that transl</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Nov</publication><modification>2025-04-05T15:59:14.934Z</modification><creation>2019-03-27T00:19:04Z</creation></dates><accession>S-EPMC2573300</accession><cross_references><pubmed>18794360</pubmed><doi>10.1128/MCB.00037-08</doi><doi>10.1128/mcb.00037-08</doi></cross_references></HashMap>