26 research outputs found

    Mouse Apolipoprotein B Editing Complex 3 (APOBEC3) Is Expressed in Germ Cells and Interacts with Dead-End (DND1)

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    encoded protein, DND1, is able to bind to the 3′-untranslated region (UTR) of messenger RNAs (mRNAs) to displace micro-RNA (miRNA) interaction with mRNA. Thus, one function of DND1 is to prevent miRNA mediated repression of mRNA. We report that DND1 interacts specifically with APOBEC3. APOBEC3 is a multi-functional protein. It inhibits retroviral replication. In addition, recent studies show that APOBEC3 interacts with cellular RNA-binding proteins and to mRNA to inhibit miRNA-mediated repression of mRNA.Here we show that DND1 specifically interacts with another cellular protein, APOBEC3. We present our data which shows that DND1 co-immunoprecipitates APOBEC3 from mammalian cells and also endogenous APOBEC3 from mouse gonads. Whether the two proteins interact directly remains to be elucidated. We show that both DND1 and APOBEC3 are expressed in germ cells and in the early gonads of mouse embryo. Expression of fluorescently-tagged DND1 and APOBEC3 indicate they localize to the cytoplasm and when DND1 and APOBEC3 are expressed together in cells, they sequester near peri-nuclear sites.The 3′-UTR of mRNAs generally encode multiple miRNA binding sites as well as binding sites for a variety of RNA binding proteins. In light of our findings of DND1-APOBEC3 interaction and taking into consideration reports that DND1 and APOBEC3 bind to mRNA to inhibit miRNA mediated repression, our studies implicate a possible role of DND1-APOBEC3 interaction in modulating miRNA-mediated mRNA repression. The interaction of DND1 and APOBEC3 could be one mechanism for maintaining viability of germ cells and for preventing germ cell tumor development

    Restricting retrotransposons: a review

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    Performance of cork and ceramic matrix composite joints for re-entry thermal protection structures

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    In view of spacecraft re-entry applications into planetary atmospheres, hybrid thermal protection systems based on cork and ceramic matrix composites are investigated. Joints of NORCOAT LIÈGE cork with C/Csingle bondSiC ceramic matrix composite were fabricated using a) high temperature commercial inorganic adhesives and b) in-situ polymerization of the cork on top of the CMC. Mechanical shear tests under ambient conditions and in liquid nitrogen are carried out. The ultimate shear strength of all the adhesive joints at room temperature varies between 0.52 and 0.78 MPa and is similar to that of the in-situ joints. At liquid nitrogen temperature the shear strength is enhanced by up to 80%, but the ultimate shear strain decreases up to 55%. The failure mode is discussed for the two types of the fabrication procedure.FP7 framework, European Project ‘‘HYDRA’’ (G.A. n. 283797), European Commission
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