Authors
M R Bezerra2; E R Freire2; F B Holetz1; J Zamudio3; A M Rezende2; D M Moura2; N Sturm3; D Campbell3; O P de-Melo-Neto2;
1 Fiocruz ParanĂ¡, Brazil; 2 Fiocruz Pernambuco, Brazil; 3 University of California, United States
Discussion
It
is well known that the control of gene expression in Trypanosomatids is primarily
mediated by post-transcriptional processes that regulate, among other events, the
recruitment of mRNAs for translation. In other eukaryotes, mRNA recruitment is
mediated by the mRNA cap binding protein, eIF4E, part of the eIF4F complex. In
trypanosomatids, six eIF4E homologues were identified, with two of those
(EIF4E3 and EIF4E4) implicated during translation initiation. Their potential
to selective recruit distinct mRNA populations for translation, however, remain
undefined. The aim of this study then was to investigate which mRNA populations
bind to EIF4E3 and EIF4E4 in Trypanosoma
brucei. Independent experiments were carried out using the native or
ectopically expressed tagged proteins in immunoprecipitation assays which were
followed by RNA extraction and SOLiD or Illumina next generation sequencing,
respectively. The Gene Ontology molecular function annotation was then used to
identify the different mRNA populations. The results indicate that although
there are mRNAs co-precipitating with both proteins, EIF4E4 seems to associate
preferentially with mRNAs encoding abundant housekeeping proteins with
structural roles, such as the ribosomal proteins. In contrast, mRNAs bound to EIF4E3
are enriched in those coding for proteins with catalytic and binding
activities. A complementary profile can then be observed, consistent with
different populations of mRNAs bound to each protein.