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ShRNA screen of factors involved in Aire-sensitive gene expression on their 3'UTR lengthening

ABSTRACT: shRNA screen of factors involved in Aire-sensitive gene expression on their 3'UTR lengthening

PROVIDER: PRJNA592171 | ENA |

REPOSITORIES: ENA

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shRNA screen of factors involved in Aire-sensitive gene expression on their 3'UTR lengthening

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Cigarette Smoking-Associated Isoform Switching and 3’ UTR Lengthening Via Alternative Polyadenylation

Project description:Cigarette Smoking-Associated Isoform Switching and 3’ UTR Lengthening Via Alternative Polyadenylation

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Progressive lengthening of 3' untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development

Project description:The 3' untranslated regions (3' UTRs) of mRNAs contain cis-acting elements for posttranscriptional regulation of gene expression. Here, we report that mouse genes tend to express mRNAs with longer 3' UTRs as embryonic development progresses. This global regulation is controlled by alternative polyadenylation and coordinates with initiation of organogenesis and aspects of embryonic development, including morphogenesis, differentiation, and proliferation. Using myogenesis of C2C12 myoblast cells as a model, we recapitulated this process in vitro and found that 3' UTR lengthening is likely caused by weakening of mRNA polyadenylation activity. Because alternative 3' UTR sequences are typically longer and have higher AU content than constitutive ones, our results suggest that lengthening of 3' UTR can significantly augment posttranscriptional control of gene expression during embryonic development, such as microRNA-mediated regulation. Two biological replicates of C2C12 growth and differentiation conditions, repesctively

2010-08-31 | E-GEOD-23871 | biostudies-arrayexpress

Progressive lengthening of 3' untranslated regions of mRNAs by alternative polyadenylation during C2C12 differentiation

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Project title: Endogenous AIRE-immunoprecipitation from primary human neutrophils

Project description:Autoimmune regulator (AIRE) is a transcriptional regulator. We here assess the role for AIRE in primary human neutrophils. We found that the functional role for AIRE in neutrophils is to regulate the extrinsic apoptotic pathway involving the Fas/TNFR death receptors and Cathepsin G and the expression of unique immune mediators.

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RNA-sequencing of Aire-ILC3 cells from wild-type and Aire-deficient mice

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Acute molecular responses to lengthening vs shortening muscle contractions

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