Abstract
Alternative splicing occurs in over 95% of protein-coding genes and contributes to the diversity of the human proteome. Apolipoprotein E receptor 2 (apoER2) is a critical modulator of neuronal development and synaptic plasticity in the brain and is enriched in cassette exon splicing events, in which functional exons are excluded from the final transcript. These alternative splicing events affect apoER2 function, as individual apoER2 exons tend to encode distinct protein functional domains. Although several apoER2 splice variants have been characterized, much work remains to understand how apoER2 splicing events modulate distinct apoER2 activities, including ligand binding specificity, synapse formation and plasticity. Additionally, little is known about how apoER2 splicing events are regulated. Often, alternative splicing events are regulated through the combinatorial action of RNA-binding proteins and other epigenetic mechanisms, however, the regulatory pathways corresponding to each specific exon are unknown in most cases. In this mini-review, we describe the structure of apoER2, highlight the unique functions of known isoforms, discuss what is currently known about the regulation of apoER2 splicing by RNA-binding proteins and pose new questions that will further our understanding of apoER2 splicing complexity.
Highlights
RNA splicing is the process by which the spliceosome, a large ribonucleoprotein complex, catalyzes the excision of introns and the ligation of exons to form precursor-mRNAs
Neurons (Minami et al, 2010), suggesting that Reelin and apoE binding to Apolipoprotein E receptor 2 (apoER2) modulates intracellular adaptor protein interaction and functions
Several additional APOER2 exons are alternatively spliced in the human brain, such as exon 6 (LDLa repeat 7) and exons 7 and 8 (EGF repeats) (Brandes et al, 1997; Kim et al, 1997; Clatworthy et al, 1999; Myant, 2010)
Summary
RNA splicing is the process by which the spliceosome, a large ribonucleoprotein complex, catalyzes the excision of introns (non-coding regions) and the ligation of exons (coding regions) to form precursor-mRNAs (pre-mRNAs). We discuss what is known regarding function, expression and regulation of each apoER2 alternative splicing event (Table 1). Ex5 is included approximately 50% of the time in total brain RNA (Kim et al, 1997), yet is absent in RNA from fetal brain and adult frontal cortex, hippocampus and cerebellum (Clatworthy et al, 1999), suggesting ex5 splicing is under spatiotemporal regulation.
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