Part of Xenopus translin is localized in the centrosomes during mitosis

Citation
A. Castro et al., Part of Xenopus translin is localized in the centrosomes during mitosis, BIOC BIOP R, 276(2), 2000, pp. 515-523
Citations number
33
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN journal
0006291X → ACNP
Volume
276
Issue
2
Year of publication
2000
Pages
515 - 523
Database
ISI
SICI code
0006-291X(20000924)276:2<515:POXTIL>2.0.ZU;2-9
Abstract
During oogenesis, maternal mRNAs are synthesised and stored in a translatio nally dormant form due to the presence of regulatory elements at the 3' unt ranslated regions (3'UTR). In Xenopus oocytes, several studies have describ ed the presence of RNA-binding proteins capable to repress maternal-mRNA tr anslation. The testis-brain RNA-binding protein (TB-RBP/Translin) is a sing le-stranded DNA- and RNA-binding protein which can bind the 3' UTR regions (Y and H elements) of stored mRNAs and can suppress in vitro translation of the mRNAs that contain these sequences. Here we report the cloning of the Xenopus homologue of the TB-RBP/Translin protein (X-translin) as well as it s expression, its localisation, and its biochemical association with the pr otein named Translin associated factor X (Trax) in Xenopus oocytes. The fac t that this protein is highly present in the cytoplasm from stage VI oocyte s until 48 h embryos and that it has been described as capable to inhibit p aternal mRNA translation, indicates that it could play an important role in maternal mRNA translation control during Xenopus oogenesis and embryogenes is. Moreover, we investigated X-translin localisation during cell cycle in XTC cells. In interphase, although a weak and diffuse nuclear staining was observed, X-translin was mostly present in the cytoplasm where it exhibited a prominent granular staining. Interestingly, part of X-translin underwent a remarkable redistribution throughout mitosis and associated with centros omes, which may suggest a new unknown role for this protein in cell cycle. (C) 2000 Academic Press.