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Printable Handouts
Navigable Slide Index
- Introduction
- What are collagens?
- Collagen family and structure
- Outline of presentation
- Collagen biosynthesis
- Human collagen nomenclature
- Type I collagen domains
- Type I collagen genes
- Collagen structural types
- OI, EDS and chondrodysplasias
- Osteogenesis imperfecta (OI)
- Epiphyseal dysplasias
- Corneal dystrophy and dysplasia
- Chondrodysplasias - summary
- Alport syndrome
- Bethlem myopathy; Ullrich MD
- Knobloch; pigment dispersion
- Epidermolysis bullosa (DEB)
- Epidermolysis bullosa (JEB)
- The Ehlers-Danlos syndrome
- Historical EDS
- Ehlers-Danlos syndrome: clinical hallmarks
- Ehlers-Danlos syndrome: common findings
- Ehlers-Danlos syndrome: types and occurrence
- Hypermobility - Beighton scale
- Genetic and molecular basis
- EDS types linked to mutated collagens
- Fibrillar collagens and EDS
- Classical (EDS I and II)
- Vascular (EDS IV)
- Arthrochalasia (EDS VIIA, B)
- Arthrochalasia - mutations in type I collagen
- EDS and enzyme deficiency (AR)
- Dermatosparaxis (EDS VIIC)
- Dermatosparaxis - biochemical analysis
- Abnormal fibrils in EDS VIIC
- Dermatosparaxis - mutations
- Kyphoscoliotic type (EDS VI)
- Overview - EDS VI
- What does lysyl hydroxylase (LH) do?
- Importance of hydroxylysines
- LH isoforms
- Characteristics of EDS VIA (1)
- Characteristics of EDS VIA (2)
- Confirmation of EDS VIA: cultured fibroblasts
- Confirmation of EDS VIA: in dermis
- Confirmation of EDS VIA: in urine
- Mutational analysis of LH1 gene
- Mutations in LH1 gene
- Common mutation in LH1 gene
- PCR detects duplicated allele
- EDS VIB - subclass of EDS VI
- Linkage of EDS VIB to LH2/LH3
- Other genes linked to EDS VIB phenotype
- Alternative splicing of LH2
- Exon 13A - alternative exon
- Tissue distribution of LH2 isoforms
- Function of LH2 transcripts?
- Collagen disorders - summary
- Acknowledgments
Topics Covered
- Collagen biosynthesis
- Collagen structural assemblies
- Linkage of disorders to collagen mutations
- Linkage of Ehlers-Danlos syndromes (EDS) to either collagen mutations or enzyme deficiencies
- Kyphoscoliotic type (EDS VIA) and Lysyl Hydroxylase (LH) deficiency
- Mutational analysis of LH1 gene
- EDS VIB
- LH isoforms
- LH2 splicing
Links
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Talk Citation
Yeowell, H. (2017, May 29). Heritable disorders of collagen [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/LVKU9260.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Heather Yeowell has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
This presentation on heritable disorders of collagen,
has been prepared by Heather Yeowell,
of Duke University Medical Center, Division of Dermatology.
0:11
Firstly, what are collagens?
They comprise of family of
extracellular matrix proteins that has tremendous tensile strength,
and play a dominant role in maintaining the structure of various tissues.
Other important functions are their involvement in
cell adhesion, chemotaxis and migration,
and their dynamic interplay with cells to regulate tissue remodeling during growth,
differentiation, morphogenesis and wound healing.
0:44
In regard to the collagen family and structure,
the collagen family now includes at least 28 distinct members,
with 46 different alpha chains.
There were more than 20 additional proteins that have collagen-like domains.
Collagens are the main extracellular proteins,
that for instance comprise over 70 percent of dry weight of dermis.
The basic structure of the collagens,
is that they consist of three polypeptide or alpha chains,
wound in a triple helix.
The chains may be identical or different.
For example, the molecule can contain two or even three different alpha chains.
The chains contain a triple helical domain of repeating Gly-X-Y sequence.
The smallest amino acid glycine,
is in the interior of the helix,
and is thus essential to maintain the structure of the triple helix.
Any other amino acid can occupy the X-Y position,
but proline is often at position X,
and hydroxyProline, or hydroxyLysine,
are only found at position Y.
The collagen presentation will begin with