The three as: Alternative splicing, alternative polyadenylation and their impact on apoptosis in immune function.
Davia BlakeKristen W LynchPublished in: Immunological reviews (2021)
The latest advances in next-generation sequencing studies and transcriptomic profiling over the past decade have highlighted a surprising frequency of genes regulated by RNA processing mechanisms in the immune system. In particular, two control steps in mRNA maturation, namely alternative splicing and alternative polyadenylation, are now recognized to occur in the vast majority of human genes. Both have the potential to alter the identity of the encoded protein, as well as control protein abundance or even protein localization or association with other factors. In this review, we will provide a summary of the general mechanisms by which alternative splicing (AS) and alternative polyadenylation (APA) occur, their regulation within cells of the immune system, and their impact on immunobiology. In particular, we will focus on how control of apoptosis by AS and APA is used to tune cell fate during an immune response.
Keyphrases
- cell cycle arrest
- immune response
- oxidative stress
- cell death
- protein protein
- endoplasmic reticulum stress
- cell fate
- binding protein
- induced apoptosis
- endothelial cells
- genome wide
- single cell
- amino acid
- bioinformatics analysis
- cell proliferation
- pi k akt
- transcription factor
- microbial community
- risk assessment
- toll like receptor
- circulating tumor