eIF4E and Interactors from Unicellular Eukaryotes

eIF4E, the mRNA cap-binding protein, is well known as a general initiation factor allowing for mRNA-ribosome interaction and cap-dependent translation in eukaryotic cells. In this review we focus on eIF4E and its interactors in unicellular organisms such as yeasts and protozoan eukaryotes. In a firs...

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Main Authors: Daniela Ross-Kaschitza, Michael Altmann
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/6/2170
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spelling doaj-030b38ce4a2546b697acf152eccf0a342020-11-25T02:04:10ZengMDPI AGInternational Journal of Molecular Sciences1422-00672020-03-01216217010.3390/ijms21062170ijms21062170eIF4E and Interactors from Unicellular EukaryotesDaniela Ross-Kaschitza0Michael Altmann1Institut für Biochemie und Molekulare Medizin (IBMM), University of Bern, 3012 Bern, SwitzerlandInstitut für Biochemie und Molekulare Medizin (IBMM), University of Bern, 3012 Bern, SwitzerlandeIF4E, the mRNA cap-binding protein, is well known as a general initiation factor allowing for mRNA-ribosome interaction and cap-dependent translation in eukaryotic cells. In this review we focus on eIF4E and its interactors in unicellular organisms such as yeasts and protozoan eukaryotes. In a first part, we describe eIF4Es from yeast species such as <i>Saccharomyces cerevisiae</i>, <i>Candida albicans</i>, and <i>Schizosaccharomyces pombe</i>. In the second part, we will address eIF4E and interactors from parasite unicellular species&#8212;trypanosomatids and marine microorganisms&#8212;dinoflagellates. We propose that different strategies have evolved during evolution to accommodate cap-dependent translation to differing requirements. These evolutive &#8220;adjustments&#8221; involve various forms of eIF4E that are not encountered in all microorganismic species. In yeasts, eIF4E interactors, particularly p20 and Eap1 are found exclusively in Saccharomycotina species such as <i>S. cerevisiae</i> and <i>C. albicans</i>. For protozoan parasites of the Trypanosomatidae family beside a unique cap4-structure located at the 5&#8242;UTR of all mRNAs, different eIF4Es and eIF4Gs are active depending on the life cycle stage of the parasite. Additionally, an eIF4E-interacting protein has been identified in <i>Leishmania major</i> which is important for switching from promastigote to amastigote stages. For dinoflagellates, little is known about the structure and function of the multiple and diverse eIF4Es that have been identified thanks to widespread sequencing in recent years.https://www.mdpi.com/1422-0067/21/6/2170translationeif4eeif4e-interactorsyeastprotozoan parasites
collection DOAJ
language English
format Article
sources DOAJ
author Daniela Ross-Kaschitza
Michael Altmann
spellingShingle Daniela Ross-Kaschitza
Michael Altmann
eIF4E and Interactors from Unicellular Eukaryotes
International Journal of Molecular Sciences
translation
eif4e
eif4e-interactors
yeast
protozoan parasites
author_facet Daniela Ross-Kaschitza
Michael Altmann
author_sort Daniela Ross-Kaschitza
title eIF4E and Interactors from Unicellular Eukaryotes
title_short eIF4E and Interactors from Unicellular Eukaryotes
title_full eIF4E and Interactors from Unicellular Eukaryotes
title_fullStr eIF4E and Interactors from Unicellular Eukaryotes
title_full_unstemmed eIF4E and Interactors from Unicellular Eukaryotes
title_sort eif4e and interactors from unicellular eukaryotes
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2020-03-01
description eIF4E, the mRNA cap-binding protein, is well known as a general initiation factor allowing for mRNA-ribosome interaction and cap-dependent translation in eukaryotic cells. In this review we focus on eIF4E and its interactors in unicellular organisms such as yeasts and protozoan eukaryotes. In a first part, we describe eIF4Es from yeast species such as <i>Saccharomyces cerevisiae</i>, <i>Candida albicans</i>, and <i>Schizosaccharomyces pombe</i>. In the second part, we will address eIF4E and interactors from parasite unicellular species&#8212;trypanosomatids and marine microorganisms&#8212;dinoflagellates. We propose that different strategies have evolved during evolution to accommodate cap-dependent translation to differing requirements. These evolutive &#8220;adjustments&#8221; involve various forms of eIF4E that are not encountered in all microorganismic species. In yeasts, eIF4E interactors, particularly p20 and Eap1 are found exclusively in Saccharomycotina species such as <i>S. cerevisiae</i> and <i>C. albicans</i>. For protozoan parasites of the Trypanosomatidae family beside a unique cap4-structure located at the 5&#8242;UTR of all mRNAs, different eIF4Es and eIF4Gs are active depending on the life cycle stage of the parasite. Additionally, an eIF4E-interacting protein has been identified in <i>Leishmania major</i> which is important for switching from promastigote to amastigote stages. For dinoflagellates, little is known about the structure and function of the multiple and diverse eIF4Es that have been identified thanks to widespread sequencing in recent years.
topic translation
eif4e
eif4e-interactors
yeast
protozoan parasites
url https://www.mdpi.com/1422-0067/21/6/2170
work_keys_str_mv AT danielarosskaschitza eif4eandinteractorsfromunicellulareukaryotes
AT michaelaltmann eif4eandinteractorsfromunicellulareukaryotes
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