Mesoderm
Middle of the three germ layers
Diploblastic - no mesoderm
Eg. jellyfish, coral, sea anemones
Caudal dysgenesis (sirenomelia)
Insufficient mesoderm formed
Defects in lower limbs, urogenital system, vertebrae
Brachyury mutant mice
Brachyury required for mesoderm differentiation
Homozygotes lack a trunk and tail and die around embryonic day 10
Heterozygotes - short tail and abnormal vertebrae
Embryonic origin of mesoderm
Forms during gastrulation
Epithelial to mesenchymal transition (EMT)
Cell adhesion molecules down-regulated
Chick mesoderm formation
Types of mesoderm
Derivatives of the mesoderm
Chordamesoderm: the Notochord
Early forming midline structure
Transient
Signalling centre / organiser
Blue = notochord
Green = somites
Red = intermediate mesoderm
Structures notochord patterns include:
Neural tube (ectoderm)
Somites (mesoderm)
Expressed signalling molecule = Sonic hedgehog (Shh)
Zebrafish notail (ntl) mutants lack a notochord:
Abnormal neural tube
Abnormal somites / muscle
Somites
Form from paraxial mesoderm
Form in pairs
Characteristic number for each species
Form anterior to posterior
Bud off from anterior end of presomitic mesoderm
Specification of the somite forming region (paraxial mesoderm)
Somite formation (chick)
Regulation of somite formation
Clock and wave front model
Expressed at the posterior of the post-somitic mesoderm and moves forward - the cells do not move - only the expression does
More than one oscillation going on at once
Fgf8 gradient from the posterior of the presomitic mesoderm (PSM)
Somites form at a specific (low) level of Fgf8
Antagonised by retinoic acid (RA) from somites
The clock - controls somite segmentation
Expression of Notch pathway targets (eg. hairy) oscillates in the PSM
Each oscillation organises pre somitic mesoderm (PSM) cell into pairs of somites
Chick:
Clock and wave front model
Integrated - the clock only functions to form somites at specific (low) levels of Fgf8
Anterior - posterior specification of somites
Somites are specialised along AP axis
AP identity specified by Hox code
Experimental evidence
Change in Hox gene expression patterns lead to changes in segment identity
Eg. Hox10 KO mouse
Lumbar to thoracic identity
Homeotic mutations - Transform one tissue type into another
Changes in expression of ‘Master control’ genes that confer identity to individual segments
Flies exhibiting homeotic transformations
→ Adult fly heads: wild type and antennapedia
(Antp - antennae transformed to 2nd thoracic leg)
→ Adult flies: wild type and bithorax mutant (haltere transformed to wings; transformation of 3rd thoracic segment to 2nd thoracic segment)
Changes in expression of two genes in two complexes
Hox gene conservation from flies to vertebrates
Changes in Hox gene expression lead to changes in neck length
→ The chick has twice as many and cervical (neck) vertebrae as the mouse
→ Caused by changes in Hox gene expression
Loss of snake forelimbs
Hoxc6 expanded - inhibits forelimb development
Different mechanism for posterior limb loss
Summary
Specification of presomitic mesoderm - Noggin v Bmp
Specification of somite identity along the AP axis - HOXs - homeosis
Formation of somites - Clock and wave front model