Transverse section of half of a chick embryo of forty-five hours' incubation. The dorsal (back) surface of the embryo is towards the top of this page, while the ventral (front) surface is towards the bottom.
Dorsum of human embryo, 2.11 mm. in length. (The older term 'primitive segments' is used to identify the somites.)
A somite is a division of the body of an animal. In vertebrates this is mainly discernible in the embryo stage, in arthropods it is a characteristic of a hypothetical ancestor.
In the developing vertebrateembryo, somites (or primitive segments in older texts) are masses of mesoderm distributed along the two sides of the neural tube and that will eventually become dermis (dermatome), skeletal muscle (myotome), and vertebrae (sclerotome).
Because the sclerotome differentiates before the other two structures, the term "dermomyotome" is sometimes used to describe the combined dermatome and myotome.[2]
The mesoderm that is lateral (proximal) to the neural tube is called paraxial mesoderm (not the part underneath, that’s chordmesdorm that becomes the notochord)
The paraxial mesoderm is initially called the “segmental plate” in chick or “unsegmented mesoderm” in other vertebrates
As the primitive streak regresses (and neural folds gather, to eventually become the neural plate), the paraxial mesoderm separates into blocks
Number of somites can be used to determine what stage of development the embryo is at (because rates of development can be affected by temperature or other factors, absolute age is not a good indicator of development)
Somites appear on both sides of the neural tube simultaneously
Flipping stuff around has no affect on which ends develop as rostral/caudal, even fully excising the tissue, it will still order itself properly and at the right times
Somite formation can be induced by Noggin-secreting cells
Number of somites is species dependent and independent of embryo size (changed via surgery or genetic engineering)
Chick: 50
Mice: 65
Snake: 500
Notch Signalling
Notch forms the boundaries of the somites
Dll1 and Dll3 are Notch ligands, mutations of which cause various defects
Notch regulates Hairy1 which sets up the caudal half of the somite
Mesp2 induces EphA4 which causes repulsive interaction that separates somites (causes segmentation)
EphA4 is restricted to the boundaries of somites
Ephrin-B2 also important for boundaries
Epithelialization of Somites
Fibronectin and N-cadherin are key to epithelialization
Probably regulated by Paraxis and mesp2
Mesp2 regulated by Notch signaling
Paraxis regulated by processes involving the cytoskeleton
Anterior-Posterior Axis Specification
Hox genes specify which somite becomes which feature
Specification occurs very early
After somites are made, they are set for what they will become, transplantation of somites results in the wrong type of vertebrae forming in the wrong place
The internal cells of the somite are not predestined
Somites Make What?
Rib and vertebrae cartilage
Muscles:
Rib cage
Limbs
Abdominal wall
Back and tongue
Dorsal skin dermis (back skin)
In crustaceans
In crustacean biology, a somite is a segment of the hypothetical primitive crustacean body plan. In current crustaceans, several of those somites may be fused.