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- Introduction
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1. Drosophila genetics - the first 25 years
- Prof. Dan Lindsley
- Establishment of the Primary Body Axes
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2. Homeotic genes in Drosophila's bithorax complex - The legacy of Ed Lewis
- Prof. Francois Karch
- Cell Type Specification and Organ Systems
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4. From germ cell specification to gonad formation
- Prof. Ruth Lehmann
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5. Drosophila stem cells
- Prof. Michael Buszczak
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6. Legacy of drosophila genetics: female germline stem cells
- Prof. Michael Buszczak
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7. Intestinal stem cell-mediated repair in Drosophila 1
- Prof. Tony Ip
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8. Intestinal stem cell-mediated repair in Drosophila 2
- Prof. Tony Ip
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10. Axon guidance in Drosophila
- Prof. John Thomas
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11. Development and physiology of the heart
- Prof. Rolf Bodmer
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12. Identification of host defenses in the Drosophila gut using genome-scale RNAi
- Prof. Dominique Ferrandon
- Genome Organization and Function
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13. The genetic analysis of meiosis in Drosophila melanogaster females
- Prof. R. Scott Hawley
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15. Dorsal-ventral patterning of the Drosophila embryo
- Prof. Mike Levine
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17. Genome-wide pooled CRISPR screen in arthropod cells
- Prof. Norbert Perrimon
- Behavior
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19. Genetics of chemosensory transduction: taste and smell
- Dr. Leslie Vosshall
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20. Cracking the case of circadian rhythms by Drosophila genetics
- Prof. Jeffrey C. Hall
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21. Sleep in Drosophila
- Dr. Ralph Greenspan
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23. Drosophila as a model for drug addiction
- Prof. Ulrike Heberlein
- Mechanism of Human Disease
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24. Cross-genomic analysis of human disease genes
- Prof. Ethan Bier
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25. Human neurodegenerative disease: insights from Drosophila genetics
- Prof. Nancy Bonini
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26. Metastasis of Drosophila tumors
- Prof. Allen Shearn
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27. Rac-enhanced CAR immunotherapy: RaceCAR
- Prof. Denise Montell
- Evolution of Adaptive Novelties
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29. The evolution of morphological novelty
- Prof. Nipam Patel
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30. The genetic architecture of complex traits: lessons from Drosophila
- Prof. Trudy Mackay
- Archived Lectures *These may not cover the latest advances in the field
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31. Using gene expression information to provide insights into patterning and differentiation
- Prof. Angelike Stathopoulos
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32. Regulation of gastrulation in Drosophila
- Prof. Dr. Maria Leptin
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33. microRNA function in stem cells
- Prof. Hannele Ruohola-Baker
Printable Handouts
Navigable Slide Index
- Introduction
- Conserved processes: Hox genes (1)
- Conserved processes: Hox genes (2)
- Diseases associated with defects in Hox genes
- Neural Induction is a conserved process
- Shared mechanisms for developmental disorders
- Common vertebrate and invertebrate ancestor
- Problems in human genetics
- Model genetic organisms
- Using the Homophila web site
- Human disease genes in flies
- Disease genes well suited for study in Drosophila
- Diseases covered in this series
- Closing-the-loop in humans
- The fly wing as genetic assay system
- Angelman syndrome
- Cross-genomic analysis of UBE3A in flies
- The GAL4/UAS expression system
- Pbl is a candidate target of UBE3A
- UBE3A reduces Pbl activity
- Faf and Pbl exert opposing activities
- dUbe3A limits Pbl levels in S2 cells
- UBE3A binds to Pbl/Ect2
- Dosage sensitivity of Ube3a/Pbl pathway
- Pbl/Ect2 misregulated in Ube3a- mice cerebellum
- Pbl/Ect2 is mis-regulated in the hippocampus
- Dosage sensitivity of UBE3A/Pbl in humans?
- Anthrax toxins: LF and EF (1)
- Anthrax toxins: LF and EF (2)
- LF Cleaves Drosophila MKKs
- LF-Toxin blocks dorsal closure
- LF disrupts actin in leading edge cells
- LF blocks dpp activation
- LF causes a hep-like phenotype
- LF suppresses the effect of activated Hep*
- EF toxin
- Hh determines spacing of the L3 and L4 veins
- EF blocks PKA-dependent Hh signaling
- Acknowledgements
Topics Covered
- Systematic cross genomic comparison revealed that 75% of human disease genes have clear homologs in Drosophila and that ≈ 30% are highly conserved sequences
- The fly is an excellent model multicellular organism for examining the mechanistic function of conserved human disease genes involved in developmental or tissue-related processes
- Normal or mutant human disease genes can be mis-expressed in the fly in localized patterns or at specific times using the GAL4-UAS mis-expression system
- Flies were used to identify candidate target proteins that are regulated by Ube3a and may contribute to Angelman syndrome
- Flies were used to examine the function and interaction of two toxins, Lethal Factor (LF) and Edema Factor (EF), that are produced by Bacillus anthracis
- LF cleaves at least two of the four Drosophila MAPKKs and inhibits the function of a third
- EF inhibits PKA dependent Hedgehog signaling in the fly wing
Talk Citation
Bier, E. (2017, September 25). Cross-genomic analysis of human disease genes [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/IPIQ3391.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Ethan Bier, Ownership Interest: Agragene and Synbal start-up companies
A selection of talks on Methods
Transcript
Please wait while the transcript is being prepared...
0:00
Hello, my name is Ethan Bier, and
today I'd like to tell you a little bit
about how fruit flies can be used to
study the mechanisms of human disease.
I refer to this often as cross-genomic
analysis of human disease genes,
that is using model organisms
like fruit flies to understand
the mechanism of human
disease gene action.
Now you might on the surface think how on
earth could you possibly use a fruit fly
which looks so very different from
a human, to study a process which seems so
intrinsically human, like human disease?
I'd like first to give a little bit of
background about how we came to this point
of thinking that this is something one
can do, and then give you some examples
of highlights of what is going to be talks
given by other people in this series
on this topic and some examples
that have come from my own lab.
But first I'd just like to give you
a little bit of the background again,
in terms of why we thought that it might
be possible to use fruit flies to study
the mechanism of human
disease gene action.
1:00
What you're looking at here is a fruit
fly embryo about half the way through
its development, and what you have here
on the left is the nose of the embryo,
then it wraps around a little
like a horseshoe to the tail,
to that tail domain that's in yellow.
And what you see are all these stripe
patterns of genes that start from
the yellow in the tail, go all the way
through the red and the blue and
the orange, green and
purple and blue to the nose.
These genes are genes that
control the identity of
different positions within the body of
the fruit fly, they're called Hox genes.
One of the very interesting things about
Hox genes is that they've been very
highly conserved in their function
during the course of evolution.