Abstract
Transient transfection of COS-1 cells with an expression vector for NIPP-1, a nuclear subunit of protein phosphatase-1, did not result in an overexpression of NIPP-1 protein, although the levels of mRNA encoding NIPP- 1 increased dramatically. Moreover, high concentrations of NIPP-1 mRNA inhibited the translation in reticulocyte lysates of various unrelated mRNAs. This inhibition of translation was caused by the NIPP-1 messenger and not by the translation product, since mutation of the start codon abolished NIPP-1 protein production, but had no influence on the translational inhibition. Analysis of deletion mutants showed that the inhibition was mediated by a 0.5-kb fragment in the 5' -end of the NIPP- 1 mRNA. This region, when inserted in the 5'-untranslated region c,f the β-galactosidase messenger, inhibited the translation of β-galactosidase mRNA in COS-1 cells. A predicted highly stable secondary structure ΔG = -239.5 kJ/mol) is present between residues 300 and 500 of NIPP-1 mRNA. The possible importance of this structure in the translational inhibition is discussed.
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Wera, S., Van Eynde, A., Stalmans, W., & Bollen, M. (1997). Inhibition of translation by mRNA encoding NIPP-1, a nuclear inhibitor of protein phosphatase-1. European Journal of Biochemistry, 247(1), 411–415. https://doi.org/10.1111/j.1432-1033.1997.00411.x
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