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Transcript Regulation of the Recoded Archaeal α-l-Fucosidase In Vivo.

Authors :
De Lise, Federica
Iacono, Roberta
Strazzulli, Andrea
Giglio, Rosa
Curci, Nicola
Maurelli, Luisa
Avino, Rosario
Carandente, Antonio
Caliro, Stefano
Tortora, Alessandra
Lorenzini, Fabio
Di Donato, Paola
Moracci, Marco
Cobucci-Ponzano, Beatrice
Saladino, Raffaele
Phylactou, Leonidas A.
Source :
Molecules; Apr2021, Vol. 26 Issue 7, p1861, 1p
Publication Year :
2021

Abstract

Genetic decoding is flexible, due to programmed deviation of the ribosomes from standard translational rules, globally termed "recoding". In Archaea, recoding has been unequivocally determined only for termination codon readthrough events that regulate the incorporation of the unusual amino acids selenocysteine and pyrrolysine, and for −1 programmed frameshifting that allow the expression of a fully functional α-l-fucosidase in the crenarchaeon Saccharolobus solfataricus, in which several functional interrupted genes have been identified. Increasing evidence suggests that the flexibility of the genetic code decoding could provide an evolutionary advantage in extreme conditions, therefore, the identification and study of interrupted genes in extremophilic Archaea could be important from an astrobiological point of view, providing new information on the origin and evolution of the genetic code and on the limits of life on Earth. In order to shed some light on the mechanism of programmed −1 frameshifting in Archaea, here we report, for the first time, on the analysis of the transcription of this recoded archaeal α-l-fucosidase and of its full-length mutant in different growth conditions in vivo. We found that only the wild type mRNA significantly increased in S. solfataricus after cold shock and in cells grown in minimal medium containing hydrolyzed xyloglucan as carbon source. Our results indicated that the increased level of fucA mRNA cannot be explained by transcript up-regulation alone. A different mechanism related to translation efficiency is discussed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14203049
Volume :
26
Issue :
7
Database :
Complementary Index
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
149715615
Full Text :
https://doi.org/10.3390/molecules26071861