The 5' untranslated region of mRNA for ribosomal protein S19 is involved in its translational regulation during Xenopus development.

Translation Embryo, Nonmammalian Transcription, Genetic Zygote Messenger Restriction Mapping Xenopus laevi animal cell Xenopus laevis Cloning, Molecular Non-U.S. Gov't Settore BIO/11 - BIOLOGIA MOLECOLARE 0303 health sciences Nonmammalian article Prokaryota priority journal Ribonucleoproteins Polyribosome Female Support Anura Transcription Ribosomal Proteins messenger rna Molecular Sequence Data embryo messenger rna; ribosome protein; age; animal cell; article; embryo; embryo development; nonhuman; priority journal; rna translation; toad; translation regulation; Animal; Base Sequence; Cloning, Molecular; DNA; Embryo, Nonmammalian; Female; Gene Expression Regulation; Genes, Structural; Molecular Sequence Data; Polyribosomes; Restriction Mapping; Ribonucleoproteins; Ribosomal Proteins; RNA, Messenger; Support, Non-U.S. Gov't; Transcription, Genetic; Translation, Genetic; Xenopus laevis; Zygote; Animalia; Anura; Felis catus; Prokaryota translation regulation Ribosomal Protein 03 medical and health sciences ribosome protein Structural Genetic Animalia Animals RNA, Messenger rna translation nonhuman Base Sequence Animal Molecular embryo development Ribonucleoprotein DNA toad age Gene Expression Regulation Genes Polyribosomes Protein Biosynthesis RNA Felis catu Cloning
DOI: 10.1128/mcb.10.2.816 Publication Date: 2015-10-01T21:52:04Z
ABSTRACT
During Xenopus development, the synthesis of ribosomal proteins is regulated at the translational level. To identify the region of the ribosomal protein mRNAs responsible for their typical translational behavior, we constructed a fused gene in which the upstream sequences (promoter) and the 5' untranslated sequence (first exon) of the gene coding for Xenopus ribosomal protein S19 were joined to the coding portion of the procaryotic chloramphenicol acetyltransferase (CAT) gene deleted of its own 5' untranslated region. This fused gene was introduced in vivo by microinjection into Xenopus fertilized eggs, and its activity was monitored during embryogenesis. By analyzing the pattern of appearance of CAT activity and the distribution of the S19-CAT mRNA between polysomes and messenger ribonucleoproteins, it was concluded that the 35-nucleotide-long 5' untranslated region of the S19 mRNA is able to confer to the fused S19-CAT mRNA the translational behavior typical of ribosomal proteins during Xenopus embryo development.
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