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
AUTHORS (2)
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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