- Phylotypic stage
- Review
(see figures 5.14 )
- notochord
- neural tube -> brain, spinal cord
- neural crest (table 5.2)
-> connective
tissue of face and pharynx, somatic sensory cranial neurons (CN
V), somatic sensory glial cells, visceral motor neurons
- neurogenic placodes (Table
5.3) -> visceral
sensory cranial neurons (olfactory, otic, lateral lines), somatic
sensory cranial neurons
- somite (paraxial mesoderm)
(Fig. 5.17)
- segmented paraxial mesoderm that is largely postcranial (the first few somites
are actually at the back of the head.
- sclerotome -> vertebral bodies, ribs, arches
- dermatome -> skin connective tissue (dermis)
- myotome -> body wall muscles, limb muscles, body wall connective
tissue
- intermediate mesoderm
(Fig. 5.17) -> urogenital systems
- lateral plate mesoderm
(Fig. 5.17)
- splanchnic -> gut connective tissue, smooth muscle of gut,
smooth muscle and connective tissue of heart and blood vessels,
extraembryonic membranes (chorion, amnion)
- somatic -> connective tissue of limb buds and parietal peritoneum
- coelom (Fig. 5.36)
- Segmentation
- trunk shows conspicuous
segmentation in its organization - that is the repeated pattern
of the same (or slight modifications of) organization. The bone
(vertebrae, ribs), muscles, and nerves all show this segmentation
although the muscle segmentation gets pretty obscured in amniotes
(segmented myotome is much easier to see in fishes in amphibians).
- Is the head segmented?
We will talk about this next week.
- Does the phylotypic stage
really exist or is it just an illusion due to the conspicuous shared
features that one can see externally (pharyngeal pouches, somites,
tail)
- Regulation of Morphology (not
much in your text) - a great deal of the differences in morphology at low
levels (conspecific, congeneric) and high levels (families, classes)
are due to difference in gene regulation. For example:
- Hox gene clusters
- 4 clusters (a-d) each with 13 subgroups (1-13). Each cluster
on a different chromosome.
- A hox protein is a transcription factor that regulates gene expression.
It has a highly conserved homeobox region that binds to DNA
and more variable region that determines where in the DNA it will
bind. This more
variable region can bind to co-factors.
- Hox genes regulate anterior posterior patterning in the animal
embryo
- Hox genes are spatially and temporally collinear. That is, the
order that they are expressed along the axis is the same order
that they are
arranged on the chromosome. And the timing of their expression
is the same as their spatial ordering on the chromosome.
- Hox genes regulate the development of the segments along the
AP axis
- Hox genes and limb growth
- the fore and hind
limbs are associated with different somites in different vertebrates,
a pattern that has always puzzled comparative vertebrate anatomists
(and has caused us to expand our definition of homology)
- It is now known that
HoxC-6 regulates the fore-limb bud and HoxC-8-10 regulate the
hind limb bud. So where HoxC-6 is expressed, a forelimb will
grow
- cervical vertebrate
form anterior to expression of HoxC-6 and the forelimb bud
grows just anterior to the most anterior expression of HoxC-6
- In the python, HoxC-6
is expressed far anteriorly so there is no cervical region
and no fore limb buds
- Some websites for Hox
gene explanations:
- http://www.ucalgary.ca/UofC/eduweb/virtualembryo/hox.html (for
hox intro in general)
- http://biology.uoregon.edu/classes/bi355f02/Topics%2002/topic%2010%2002.html (not as good as an intro but look at the snake story at the end).
- Sonic Hedgehog (SHH)
- SHH regulates AP patterning
in the limb bud. There is a recent new study that shows that the duration
of its expression in the limb bud
of the skink Hemiargis determines how many digits the skin has. Short
duration = 2 digits. Intermediate duration = 3-4 digits. Long duration
= 5 digits. This is a type of heterochrony. There is more to the story
than this too!