Cargando…

Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids

Trypanosomatids are ancient eukaryotic parasites that migrate between insect vectors and mammalian hosts, causing a range of diseases in humans and domestic animals. Trypanosomatids feature a multitude of unusual molecular features, including polycistronic transcription and subsequent processing by...

Descripción completa

Detalles Bibliográficos
Autores principales: Zinoviev, Alexandra, Shapira, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399392/
https://www.ncbi.nlm.nih.gov/pubmed/22829751
http://dx.doi.org/10.1155/2012/813718
_version_ 1782238404016078848
author Zinoviev, Alexandra
Shapira, Michal
author_facet Zinoviev, Alexandra
Shapira, Michal
author_sort Zinoviev, Alexandra
collection PubMed
description Trypanosomatids are ancient eukaryotic parasites that migrate between insect vectors and mammalian hosts, causing a range of diseases in humans and domestic animals. Trypanosomatids feature a multitude of unusual molecular features, including polycistronic transcription and subsequent processing by trans-splicing and polyadenylation. Regulation of protein coding genes is posttranscriptional and thus, translation regulation is fundamental for activating the developmental program of gene expression. The spliced-leader RNA is attached to all mRNAs. It contains an unusual hypermethylated cap-4 structure in its 5′ end. The cap-binding complex, eIF4F, has gone through evolutionary changes in accordance with the requirement to bind cap-4. The eIF4F components in trypanosomatids are highly diverged from their orthologs in higher eukaryotes, and their potential functions are discussed. The cap-binding activity in all eukaryotes is a target for regulation and plays a similar role in trypanosomatids. Recent studies revealed a novel eIF4E-interacting protein, involved in directing stage-specific and stress-induced translation pathways. Translation regulation during stress also follows unusual regulatory cues, as the increased translation of Hsp83 following heat stress is driven by a defined element in the 3′ UTR, unlike higher eukaryotes. Overall, the environmental switches experienced by trypanosomatids during their life cycle seem to affect their translational machinery in unique ways.
format Online
Article
Text
id pubmed-3399392
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-33993922012-07-24 Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids Zinoviev, Alexandra Shapira, Michal Comp Funct Genomics Review Article Trypanosomatids are ancient eukaryotic parasites that migrate between insect vectors and mammalian hosts, causing a range of diseases in humans and domestic animals. Trypanosomatids feature a multitude of unusual molecular features, including polycistronic transcription and subsequent processing by trans-splicing and polyadenylation. Regulation of protein coding genes is posttranscriptional and thus, translation regulation is fundamental for activating the developmental program of gene expression. The spliced-leader RNA is attached to all mRNAs. It contains an unusual hypermethylated cap-4 structure in its 5′ end. The cap-binding complex, eIF4F, has gone through evolutionary changes in accordance with the requirement to bind cap-4. The eIF4F components in trypanosomatids are highly diverged from their orthologs in higher eukaryotes, and their potential functions are discussed. The cap-binding activity in all eukaryotes is a target for regulation and plays a similar role in trypanosomatids. Recent studies revealed a novel eIF4E-interacting protein, involved in directing stage-specific and stress-induced translation pathways. Translation regulation during stress also follows unusual regulatory cues, as the increased translation of Hsp83 following heat stress is driven by a defined element in the 3′ UTR, unlike higher eukaryotes. Overall, the environmental switches experienced by trypanosomatids during their life cycle seem to affect their translational machinery in unique ways. Hindawi Publishing Corporation 2012 2012-07-08 /pmc/articles/PMC3399392/ /pubmed/22829751 http://dx.doi.org/10.1155/2012/813718 Text en Copyright © 2012 A. Zinoviev and M. Shapira. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Zinoviev, Alexandra
Shapira, Michal
Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids
title Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids
title_full Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids
title_fullStr Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids
title_full_unstemmed Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids
title_short Evolutionary Conservation and Diversification of the Translation Initiation Apparatus in Trypanosomatids
title_sort evolutionary conservation and diversification of the translation initiation apparatus in trypanosomatids
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399392/
https://www.ncbi.nlm.nih.gov/pubmed/22829751
http://dx.doi.org/10.1155/2012/813718
work_keys_str_mv AT zinovievalexandra evolutionaryconservationanddiversificationofthetranslationinitiationapparatusintrypanosomatids
AT shapiramichal evolutionaryconservationanddiversificationofthetranslationinitiationapparatusintrypanosomatids