Propagation of the Treacher Collins Syndrome Mouse Model - PowerPoint PPT Presentation

1 / 33
About This Presentation
Title:

Propagation of the Treacher Collins Syndrome Mouse Model

Description:

Propagation of the Treacher Collins Syndrome Mouse Model By Heather Dawn Cross Mentor: Dr. Rita Shiang Grad Student: Michelle Holser What is Treacher Collins A rare ... – PowerPoint PPT presentation

Number of Views:76
Avg rating:3.0/5.0
Slides: 34
Provided by: HeatherD59
Learn more at: https://cbds.vcu.edu
Category:

less

Transcript and Presenter's Notes

Title: Propagation of the Treacher Collins Syndrome Mouse Model


1
Propagation of the Treacher Collins Syndrome
Mouse Model
  • By Heather Dawn Cross
  • Mentor Dr. Rita Shiang
  • Grad Student Michelle Holser

2
Working in the lab Loading a gel
3
Dr. Rita Shiang, my mentor, looking over some
pictures I took.
4
Michelle my grad student mentor
5
What is Treacher Collins
  • A rare genetic disorder
  • Characterized by
  • Abnormal or absent external ear
  • Hearing loss
  • Very small lower jaw
  • Defect in lower eye
  • Cleft palate
  • Breathing problems
  • Down slanting eyes

6
The Genetics
  • The Treacher Collins gene, identified as TCOF1,
    is located on the 5th chromosome, and codes for
    the protein treacle.
  • The disorder is autosomal dominant.
  • The protein, treacle, is involved in craniofacial
    development in embryos

7
Treacher Collins Gene
8
Cre/LoxP System
  • Cre- cyclization recombination,
  • loxP - locus of X-over P1,34 base pairs where Cre
    can bind to recombine the DNA

9
Basic Idea
10
Our Timed Mating Scheme
?
?
Heterozygous for Cre and loxP
1A5-N-1 or 1A5-N-3
11
Our Timed Mating Scheme
These are the homozygous knockout mice that we
are studying.
12
The Timed Matings
  • These timed matings are used for dissections to
    characterize the model.
  • They are dissected at specific time points
  • 8.5 dpc
  • 9.5 dpc
  • 10.5 dpc
  • 11.5 dpc
  • 12.5 dpc

13
Embryos
  • The yolk sac from each embryo is genotyped to
    separate out the homozygous knockouts,
    heterozygous knockouts and wild types.
  • The embryos are collected until there are some
    homozygous knockouts for each developmental
    stage.
  • At this point, various experiments can be
    performed with the embryos.

14
Tcof1 -/- homozygotes Vs. Wildtype
15
Tcof1 -/- homozygotes Vs. Wildtype
16
Mouse Embryos with Tek Staining
Tcof1 -/- homozygotes
Wildtype Embryos
17
B6 Background Transfer
  • Transferring the 1A5-N-1 and the 1A5-N-3 lines
    from a SV/J to a B6 mouse genetic background,
    because the B6 mice show a phenotype similar but
    more severe to Treacher Collins Syndrome.
  • It takes 10 generations for each mouse line to be
    considered transferred.

18
Transfer Mating
1A5-N-1 or 1A5-N-3 generation 1
B6
?
?
?
?
?
?
19
N-1-B6-02 or N-3-B6-02 generation 2
We keep only the positive males to be mated to
female B6 to continue the background transfer.
This will continue till we reach the 10th
generation of mice.
20
Genotyping
  • Each pup or embryo goes through genotyping
  • The DNA is extracted from an ear punch or the
    yolk sac tissue
  • The DNA is amplified by PCR
  • The DNA is then run on a gel forming a set of
    lines that defines the genotype

21
The reason for the fragments in gels
The amplified Cre fragment being the longest
would run the slowest in a gel The addition of
the LoxP sites makes the PCR fragment of the gene
longer so when separated in a gel it would be
slower than the natural gene.
22
Reading the Gel
Cre line
Heterozygous for loxP
Homozygous for loxP
Homozygous for wild type
23
Embryo Gel
24
An Actual Gel, Pups
25
Actual Gel, Embryos
26
Other Gels
27
My Role
  • My responsibilities include helping with
  • the general care of the mice
  • keeping the mouse lines alive and properly mated
  • genotyping the pups and embryos
  • DNA extractions
  • PCR
  • gels
  • timed mating dissections
  • Processing embryos

28
Pictures of Me at Work
29
What Happened
  • During the summer we were able to collect mice
    from
  • 8.5 dpc
  • 9.5 dpc
  • 10.5 dpc
  • 11.5 dpc
  • Due to 2 different false pregnancies in the mice
    we were unable to collect mice from the 12.5 dpc
  • This resulted in the inability to
  • continue on with any further
  • experimentation

30
Something New
  • I was honored enough to see something that Dr.
    Shiang has never seen before in a timed
    dissection.
  • On July 19th while doing a 9.5 dpc dissection, I
    found a set of identical twins in the embryos.
  • Normally each embryo has its own bead and yolk
    sac but there were 2 embryos in one bead
    sharing a yolk sac.

31
This summer
  • This summer I learned a lot about research
  • It doesn't always work
  • Some days are exciting and some are not
  • Working in a lab group is a unique experience
  • Research is something that I could see myself
    doing in the future
  • The mice do not always get
  • pregnant when you want them to!

32
ANY QUESTIONS?
  • Thank you for your time and attention!

33
Sites used for presentation
  • http//mouseworksonline.com/
  • http//phenome.jax.org/pub-cgi/phenome/mpdcgi?rtn
    docs/home
  • http//www.scq.ubc.ca/?p287
  • http//ghr.nlm.nih.gov/genetcof1
  • http//www.nlm.nih.gov/medlineplus/article/001659.
    htm
  • http//www.treachercollins.org/main.html
Write a Comment
User Comments (0)
About PowerShow.com