Abstract

Control of gene expression in erythropoiesis has to respond to signals that may emerge from intracellular processes or environmental factors. Control of mRNA translation allows for relatively rapid modulation of protein synthesis from the existing transcriptome. For instance, the protein synthesis rate needs to be reduced when reactive oxygen species or unfolded proteins accumulate in the cells, but also when iron supply is low or when growth factors are lacking in the environment. In addition, regulation of mRNA translation can be important as an additional layer of control on top of gene transcription, in which RNA binding proteins (RBPs) can modify translation of a set of transcripts to the cell’s actual protein requirement. The 5′ and 3′ untranslated regions of mRNA (5′UTR, 3′UTR) contain binding sites for general and sequence specific translation factors. They also contain secondary structures that may hamper scanning of the 5′UTR by translation complexes or may help to recruit translation factors. In addition, the term 5′UTR is not fully correct because many transcripts contain small open reading frames in their 5′UTR that are translated and contribute to regulation of mRNA translation. It is becoming increasingly clear that the transcriptome only partly predicts the proteome. The aim of this review is (i) to summarize how the availability of general translation initiation factors can selectively regulate transcripts because the 5′UTR contains secondary structures or short translated sequences, (ii) to discuss mechanisms that control the length of the mRNA poly(A) tail in relation to mRNA translation, and (iii) to give examples of sequence specific RBPs and their targets. We focused on transcripts and RBPs required for erythropoiesis. Whereas differentiation of erythroblasts to erythrocytes is orchestrated by erythroid transcription factors, the production of erythrocytes needs to respond to the availability of growth factors and nutrients, particularly the availability of iron.

Highlights

  • Reviewed by: Eitan Fibach, Hadassah Medical Center, Israel Andrew Charles Perkins, Monash University, Australia Theodosia A

  • GATA1 protein synthesis is reduced in Diamond-Blackfan anemia (DBA), a congenital red cell aplasia caused by reduced biosynthesis of ribosomes, and mutations in GATA1 can cause a DBA-like phenotype (Ludwig et al, 2014; Vlachos et al, 2014; Paolini et al, 2016)

  • Because the recruitment of polyadenylating or deadenylating complexes depends on the context of the transcripts, i.e., on the complexes formed with RNA binding proteins (RBPs) that bind to nearby elements in the 3 UTR, CPEB4 enhances or decreases mRNA translation with transcript-specific regulation

Read more

Summary

RNA Binding Proteins and Regulation of mRNA Translation in Erythropoiesis

The 5 and 3 untranslated regions of mRNA (5 UTR, 3 UTR) contain binding sites for general and sequence specific translation factors. They contain secondary structures that may hamper scanning of the 5 UTR by translation complexes or may help to recruit translation factors. The aim of this review is (i) to summarize how the availability of general translation initiation factors can selectively regulate transcripts because the 5 UTR contains secondary structures or short translated sequences, (ii) to discuss mechanisms that control the length of the mRNA poly(A) tail in relation to mRNA translation, and (iii) to give examples of sequence specific RBPs and their targets.

GENE EXPRESSION AND SIGNAL TRANSDUCTION SET THE STAGE FOR ERYTHROPOIESIS
RNA Binding Proteins in Erythropoiesis
Epo and SCF Controlled Translational Initiation in Erythroblasts
Upstream Open Reading Frames
AUBPs in Hematopoiesis
Alternative Polyadenylation Controls mRNA Stability and Translation
RBPs INVOLVED IN ADDITIONAL CONTROL OF TRANSLATION
Translational Control of Iron Homeostasis
More RBPs and Methods to Decipher Translation Efficiency
CONCLUSION
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call