Please describe the procedure / two effects of alternative splicing.
Process of Splicing (two steps):
5 critical bases: 5’ donor SS (GU), branch point (A), 3’ acceptor SS (AG)
first step:
cleavage at the 5’ SS
joining of the 5′ end of the intron to an A within the intron (the branch point)
—> lariat-like (lasso) intermediate —> intron forms a loop
second step:
cleavage at the 3′ splice site and ligation of the exons
—> result: excision of the intron as a lariat-like structure
Effects of AS:
multiple isoforms of a gene —> Protein diversity
Tissue-specific regulation of gene expression
What are the consequences if the protein product becomes larger as a result?
Larger product:
Change protein stability
Change enzymatic/ signaling activity
Explain positive and negative control of AS.
Negative control
repressor protein binds to the primary RNA in tissue 2
prevents intron removal by the splicing machinery
Positive control
splicing machinery needs activator protein to remove intron sequence efficiently
How many genes are included in the human genome? How much percent of them are estimated to undergo AS?
~ 25.000 genes
> 35% undergo AS
List different types of AS.
What are the two types of alternative splicing?
constitutive:
always > 1 isoform per pre-mRNA
regulated:
splicing forms depends on tissue/condition/time
What are the roles of AS?
add protein parts: 75% of AS in CDS —> change structure
stability (e.g., inclusion of cleavage sites)
alter enzymatic or signaling activities
alter protein binding (e.g., receptor/ligand)
alter 5’ / 3’ UTR regions:
RNA either degraded or not
RNA in cytoplasm or exported
regulation of biological events:
Cell differentiation
Neuron development
Apoptosis
What is an EST?
Expressed sequence tag
cDNA -> RNA that start from either
5’ -> 5’ EST
3’ -> 3’ EST
Explain an approach to computational AS detection.
Insertion and deletion in Expressed Sequence Tags (ESTs) relative to mRNA
two splice sites are mutually exclusive —> check donor/acceptor site (are highly conserved, 99.24% of introns have a GT-AG at their 5′ and 3′ ends)
—> heavily depends on ESTs
How can you experimentally detect AS?
—> analyzing RNA isoforms
using RT-PCR with primers that flank the alternatively spliced region → different lengths of PCR product
using microarrays (high-throughput approach) with exon-exon junction probes
Explain a measure of dissimilarity between mRNA isoforms.
Computation of splice junction difference ratio (SJD)
—> 0 = the same, 1 = completely different
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