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Printable Handouts
Navigable Slide Index
- Introduction
- Typical eukaryotic gene
- Typical eukaryotic intron
- Spliceosomal catalysis
- Group II self splicing intron
- Splicing cycle
- Step 2 snRNAs
- snRNAs and group II introns
- Spliceosome: the largest known cellular machine
- Spliceosome complexity
- Results from splicing mistakes
- Splicing and disease
- Alternative splicing
- Types of alternative splicing
- Extent of alternative splicing
- Overview of splicing regulatory mechanisms
- Exon junction complex
- Nonsense mediated decay
- Summary
Topics Covered
- Recognition of splice junction sequences by components of the spliceosome
- Spliceosome assembly, catalysis and disassembly
- Roles of snRNPs as well as non-snRNP components
- RNA dependent ATPases
- Splicing in creating multiple mRNAs
Talk Citation
Nilsen, T. (2015, July 23). Pre-mRNA splicing [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/OOTD7214.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Timothy Nilsen has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Pre-mRNA splicing
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
The focus of this presentation
is Nuclear Pre-mRNA Splicing.
Splicing is an essential
step in the expression
of almost all genes
and higher eukaryotes.
We will begin by discussing
the phenomenon of splicing
and then discuss the
mechanism by which it occurs.
We will then shift to a discussion
of how splicing, specifically
alternative splicing, contributes
to proteomic diversity.
Finally, we will briefly discuss
the role of splicing in messenger
RNA surveillance
and quality control.
0:32
This slide illustrates the
structure of a typical higher
eukaryotic protein coding gene.
The transcribed region is
shown in green and yellow,
and the flanking regions
are shown in red.
The actual coding sequence,
comprised of multiple exons,
is shown in dark green.
This sequence is interrupted by
multiple intervening sequences,
or introns, which
are shown in yellow.
Upon transcription, a
pre-mRNA is produced which
contains all of the
exons and introns.
To produce a functional
messenger RNA,
the introns must be
removed by splicing,
and the exons must be
fused together in the order
in which they were transcribed.
1:14
Here is a representation of
a typical pre-mRNA intron.
The intron contains three
important sequence elements.
Two of these elements, the five
prime and three prime splice sites,
define the boundaries of the intron.
The third element, which resides
just upstream of the three
prime splice site, is
called the branch point.
As we will see in a
moment, the branch point
is essential for the
chemistry of splicing.
Comparison of the sequences
of many thousands of introns
has revealed that each of the
three important intronic sites
is characterized by
a consensus sequence.
However, with the exception of
the first and last two nucleotides
of the intron in the branch point
itself, which are nearly invariant,
considerable variation is
allowed at all three sites.
We will come back
to this variability
in splicing signals later.