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Updated: Aug 9, 2026

Activation of Apoptosis by Cytoplasmic Microinjection of Cytochrome c
Published on: June 29, 2011
Initiation factor modifications in the preapoptotic phase
S J Morley1, M J Coldwell, M J Clemens
1Department of Biochemistry, School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QG, UK. s.j.morley@sussex.ac.uk
Abstract:
Recent studies have identified several mechanistic links between the regulation of translation and the process of apoptosis. Rates of protein synthesis are controlled by a wide range of agents that induce cell death, and in many instances, the changes that occur to the translational machinery precede overt apoptosis and loss of cell viability. The two principal ways in which factors required for translational activity are modified prior to and during apoptosis involve (i) changes in protein phosphorylation and (ii) specific proteolytic cleavages. In this review, we summarise the principal targets for such regulation, with particular emphasis on polypeptide chain initiation factors eIF2 and eIF4G and the eIF4E-binding proteins. We indicate how the functions of these factors and of other proteins with which they interact may be altered as a result of activation of apoptosis and we discuss the potential significance of such changes for translational control and cell growth regulation.
Insights
Cell death involves changes in protein synthesis regulation. Key translation factors like eIF2 and eIF4G are modified by phosphorylation and cleavage during apoptosis, impacting cell growth.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Emerging evidence links translation regulation to apoptosis.
- Protein synthesis rates are modulated by cell death inducers.
- Changes in translational machinery often precede observable apoptosis.
Purpose of the Study:
- To review mechanistic links between translation control and apoptosis.
- To highlight key regulatory modifications of translation factors.
- To discuss the implications for cell growth regulation.
Main Methods:
- Literature review of studies on translation and apoptosis.
- Focus on protein phosphorylation and proteolytic cleavage.
- Analysis of specific translation initiation factors (eIF2, eIF4G) and eIF4E-binding proteins.
Main Results:
- Identified phosphorylation and cleavage as primary mechanisms regulating translation during apoptosis.
- Detailed how eIF2, eIF4G, and eIF4E-binding proteins are affected.
- Showcased altered functions of these factors and interacting proteins.
Conclusions:
- Apoptosis involves significant alterations in translational control.
- These changes in translation factors are crucial for regulating cell death and growth.
- Understanding these mechanisms offers insights into cell fate determination.
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