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Printable Handouts
Navigable Slide Index
- Introduction
- The Pyle Lab
- What is an intron?
- Introns are not always junk...
- Different classes of introns
- Autocatalytic group I and group II introns
- Discovery of self-splicing
- Converting a self-splicing RNA into an enzyme
- The "Tetrahymena ribozyme" and RNA catalysis
- Tetrahymena ribozyme was a powerful tool
- Tetrahymena ribozyme - mechanistic enzymology
- New insights into molecular recognition of RNA
- Framing the "RNA folding problem"
- Group I intron diversity
- Group I intron structure and catalytic mechanism
- Group I intron mobility and reverse-splicing
- Group I intron applications
- Group II introns and the big picture
- First glimpse of the group II introns
- Discovery of self-splicing by group II introns
- Chemical mechanism of group II intron reactions
- Important reactions catalyzed by group II introns
- Group II introns are retroelements
- Conservation of group II intron secondary structure
- What is so interesting about group II introns?
- Catalytic engines for driving eukaryotic evolution
- Three classes of group II introns
- Functional anatomy of a group II intron
- Group II introns are strikingly modular
- Probing the transition-state with group II ribozymes
- Explaining specificity of group II ribozymes
- A model systems for RNA folding
- Suitable contruct for folding studies
- Evidence of group II folding
- RNA can have a complex folding landscape
- D135 ribozyme folds directly to native state
- Conclusions for the folding pathway
- A model systems for RNA tertiary structure
- Group II introns can react in pieces
- Domain 5: the heart of the active-site
- Different functions for two sides of domain 5
- Nuclotide analog interference mapping (1)
- Nuclotide analog interference mapping (2)
- Current map of important atoms
- Nucelotide analog interference suppression (1)
- Nucelotide analog interference suppression (2)
- The lamda-lamda prime interaction
- Where is the branch point in the catalytic core?
- Network of functional - knits the intron together
- A three-dimensional model of the ai5-gamma intron
- Close-up view of the active site
- Group II introns: the future
- Generalitiy of "branching reactions"
- Group II introns as tools and therapeutics
- Group II introns and the proteins that love them
- Special thanks
Topics Covered
- Different classes of introns
- Autocatalytic group I and group II introns
- Discovery of self-splicing
- Converting a self-splicing RNA into a multiple-turnover enzyme
- The "tetrahymena ribozyme" and discovery of RNA catalysis
- New insights into molecular recognition of RNA
- Group I intron structure and catalytic mechanism
- Group I intron applications
- Group II introns and the big picture
- Discovery of self-splicing by group II introns
- Chemical mechanism of group II intron reactions
- Catalytic engines for driving eukaryotic evolution
- Explaining specificity of group II ribozymes
- Group II intron ribozymes as model systems for RNA folding
- Group II ribozymes as model systems for RNA tertiary structure
- Nucleotide analog interference mapping
- Current map of important atoms
- Nucleotide analog interference suppression
- Lambda-lambda interaction
- 3D model of ai5gamma intron
- Group II introns as tools and therapeutics
Talk Citation
Pyle, A.M. (2016, January 19). Self-splicing intron RNAs: ribozymes, parasites and agents of genomic change [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/IKTS8261.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Anna Marie Pyle has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Self-splicing intron RNAs: ribozymes, parasites and agents of genomic change
A selection of talks on Cell Biology
Transcript
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0:00
In this talk, we'll be going over the characteristics of the self-splicing intron RNAs,
which include the group one and the group two introns,
and hopefully by the end,
you'll see what kinds of properties they have as ribozymes, as folded RNAs,
and see what kind of context they have biologically
as parasites and agents of genomic change.
0:22
The latter part of the talk will
include experiments that were done primarily in my own lab,
and your narrator is indicated by the yellow arrow in this picture.
But it's important to say that much of the talk will also be about group
one introns and I worked on those as a postdoc in Tom Cech's lab.
0:41
Before we review the specifics of group one and group two introns,
it's important to review what an intron actually is.
When a gene is actually transcribed into RNA,
there are regions of the RNA that contain information
that is not supposed to make its way into the functional product.
And these intervening regions of sequence,
which I've shown here in blue are called introns.
The functional regions of the RNA are called exons,
shown here as exon 1 and exon 2.
Through the process of splicing,
introns are removed and discarded and
the exons are stitched together again to create a functional gene.
It's important to point out that a typical gene,
encoding one of your proteins, i.e.
a eukaryotic gene, is highly complex and requires
the splicing of many exons and removal of many introns.
So splicing is a fundamental process in gene expression, particularly in eukaryotes.
1:34
So what happens with these discarded introns?
Well, sometimes they are indeed junk that requires recycling,
but sometimes introns are innately useful,
and they serve other functions in a cell.
They can encode proteins,
they can encode small regulatory RNAs such as micro RNAs or small RNAs involved in RNAi.
The splicing of introns and the sequence
of splicing can be contribution to gene expression,
but more pertinent to today's talk is that some introns are genomic parasites.
Group one and group two introns are mobile genetic elements,
that can hop from place to place within a genome or hop
from genome to genome, thereby affecting evolution.
There are four major categories of intron and each of
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