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Printable Handouts
Navigable Slide Index
- The Regulation of Pre-messenger RNA Splicing
- mRNAs are transcribed as precursor molecules
- mRNA must undergo RNA processing reactions
- Pre-mRNA splicing
- The signals for splicing RNA are at the intron ends
- Splicing proceeds by a two-step pathway
- Splicing chemistry
- Pre-mRNAs contain multiple exons and introns
- The spliceosome
- Structures of the spliceosomal snRNAs
- The spliceosome assembles from snRNPs
- The mature catalytic spliceosome
- Minor class introns
- Two features that affect splice site choice
- The early choice of splice sites to pair
- Additional controls on spliceosome assembly
- A typical mammalian gene
- Exon definition
- SR proteins
- SR proteins mediate the activity of ESEs
- Mutations in splice sites
- Human disease mutations that alter splicing
- Alternative splicing can produce diverse proteins
- Complex transcription units
- The fibronectin gene
- Patterns of alternative splicing
- Alternative splicing generates protein diversity
- The Drosophila DSCAM receptor
- Gene number and complexity of the organism
- More than ESE's
- Somatic sexual development in the fruit fly
- Sex-lethal is a sequence-specific RNA BP
- The female Sxl protein regulates itself and Tra
- Tra exon 2 has two possible 3' splice sites.
- The upstream Tra 3' splice site
- The female specific protein Tra is splicing regulator
- Doublesex exon 4 contains a weak 3' splice site
- The doublesex ESEs are dependent on Tra
- Male and female mRNAs of Dsx produce TFs
- Splicing regulation in vertebrates
- Clusters of RNA elements
- Many RNA binding proteins regulate splicing
- Alternative splicing in the nervous system
- The electrical properties of K+ channels
- Cochlear hair cells
- Some splicing regulators are tissue specific
- Widely expressed splicing regulators
- Problems for the future
Topics Covered
- Molecular mechanisms of the basic splicing reaction
- Spliceosome assembly
- Exon definition
- Splicing enhancer and silencer elements
- RNA binding proteins that regulate splicing
- Protein diversity in metazoan organisms
- Tissue specific splicing
- Drosophila sex determination pathway
- Complex regulation of alternative splicing in mammals
Talk Citation
Black, D. (2007, October 1). The regulation of Pre-Messenger RNA splicing [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/AXJP1598.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Douglas Black has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Genetics & Epigenetics
Transcript
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0:00
The regulation of pre-messenger RNA splicing.
The regulation of eukaryotic gene expression is controlled in diverse ways.
In addition to the primary mechanisms that turn the transcription of a gene on and off,
there are many post-transcriptional steps downstream in the gene expression pathway,
where the protein output of a gene can be modulated.
In this talk, I'll describe the regulation of the pre-mRNA splicing reaction,
and how this reaction can be adjusted to produce
multiple mRNAs and hence, protein products from the same gene.
This type of regulation is often called alternative splicing.
0:39
In prokaryotic cells, the primary RNA transcript
of a gene can be directly translated into protein.
However, in eukaryotes, things are much more complex.
In eukaryotic cells, mRNAs are transcribed as long precursor molecules that must undergo
several RNA processing reactions prior to
exportation from the nucleus and translation in the cytoplasm.
1:01
The first processing reaction is the addition of
a special methylated guanosine nucleotide to the five-prime end of the RNA transcript.
This cap nucleotide is connected via special
five-prime to five-prime phosphotriester linkage directly to the first nucleotide of the RNA transcript.
At the other end of the gene,
a two-step processing reaction takes place called cleavage and polyadenylation.
This involves, first, removal of the three-prime end of the RNA by
an endonucleolytic cleavage at a special sequence, the poly(A) site.
After removal of the 3-prime piece, a special enzyme,
the poly(A) polymerase, adds
between 100 and 250 adenosine residues to the new three-prime end,
creating a three-prime poly(A) tail on the RNA.
Both capping and polyadenylation are
coupled to the transcription of the RNA polymerase II
and are important for the subsequent processing, transport,
and translation of the mRNA,
and the maintenance of its stability.
The third RNA processing reaction is pre-mRNA splicing,
which involves the clipping out of internal or, intervening sequences from
the RNA and the joining, or ligation, of the remaining segments together.
The segments that are removed from the RNA are called introns,
and the segments in the sequence that remain in the final mRNA transcript are called exons.
Both cleavage, polyadenylation, and splicing are regulated by similar mechanisms
but, in this talk, we will only discuss splicing.
The most complex RNA processing reaction in the cell is pre-mRNA splicing.