Deuterostome


Deuterostomes constitute a superphylum of animals. It is a sister clade of Protostomia, with which it forms the Nephrozoa clade.
Deuterostomia is a subtaxon of the Bilateria branch of the subkingdom Eumetazoa, within Animalia, and are distinguished from protostomes by their deuterostomic embryonic development; in deuterostomes, the first opening becomes the anus, while in protostomes, it becomes the mouth.
Deuterostomes are also known as enterocoelomates because their coelom develops through enterocoely.
There are three major clades of deuterostomes:

History

Initially, Deuterostomia included the phyla Brachiopoda, Bryozoa, Chaetognatha, and Phoronida based on morphological and embryological characteristics. However, Superphylum Deuterostomia was redefined in 1995 based on DNA molecular sequence analyses when the lophophorates were removed from it and combined with other protostome animals to form superphylum Lophotrochozoa. The phylum Chaetognatha may belong here, but molecular studies have placed them in the protostomes more often.

Classification

These are the following phyla/subgroups of the deuterostomes:
Echinodermata and Hemichordata form the clade Ambulacraria. Moreover, there is a possibility that Ambulacraria can be the sister clade to Xenacoelomorpha, and form the Xenambulacraria group.

Notable characteristics

In both deuterostomes and protostomes, a zygote first develops into a hollow ball of cells, called a blastula. In deuterostomes, the early divisions occur parallel or perpendicular to the polar axis. This is called radial cleavage, and also occurs in certain protostomes, such as the lophophorates.
Most deuterostomes display indeterminate cleavage, in which the developmental fate of the cells in the developing embryo are not determined by the identity of the parent cell. Thus, if the first four cells are separated, each cell is capable of forming a complete small larva; and if a cell is removed from the blastula, the other cells will compensate.
In deuterostomes the mesoderm forms as evaginations of the developed gut that pinch off, forming the coelom. This is called enterocoely.
Another feature present in both the Hemichordata and Chordata is pharyngotremy; the presence of spiracles or gill slits into the pharynx, which is also found in some primitive fossil echinoderms. A hollow nerve cord is found in all chordates, including tunicates. Some hemichordates also have a tubular nerve cord. In the early embryonic stage, it looks like the hollow nerve cord of chordates.
Because of the highly modified nervous system of echinoderms, it is not possible to discern much about their ancestors in this matter, but based on different facts it is quite possible that all the present deuterostomes evolved from a common ancestor that had pharyngeal gill slits, a hollow nerve cord, circular and longitudinal muscles and a segmented body.

Formation of mouth and anus

The defining characteristic of the deuterostome is the fact that the blastopore becomes the anus, whereas in protostomes the blastopore becomes the mouth. The deuterostome mouth develops at the opposite end of the embryo from the blastopore and a digestive tract develops in the middle, connecting the two.
In many animals these early development stages later evolved in ways that no longer reflect these original patterns. For instance, humans have already formed a gut tube at the time of formation of the mouth and anus. Then the mouth forms first, during the fourth week of development, and the anus forms four weeks later, temporarily forming a cloaca.

Origins and evolution

The majority of animals more complex than jellyfish and other Cnidarians are split into two groups, the protostomes and deuterostomes. Chordates are deuterostomes. It seems likely that the Kimberella was a member of the protostomes. That implies that the protostome and deuterostome lineages split some time before Kimberella appeared — at least, and hence well before the start of the Cambrian, i.e. during the later part of the Ediacaran Period. The oldest discovered proposed deuterostome is Saccorhytus coronarius, which lived approximately 540 million years ago. The researchers that made the discovery believe that the Saccorhytus is a common ancestor to all previously-known deuterostomes.
Fossils of one major deuterostome group, the echinoderms, are quite common from the start of Series 2 of the Cambrian,. The Mid Cambrian fossil Rhabdotubus johanssoni has been interpreted as a pterobranch hemichordate. Opinions differ about whether the Chengjiang fauna fossil Yunnanozoon, from the earlier Cambrian, was a hemichordate or chordate. Another Chengjiang fossil, Haikouella lanceolata, also from the Chengjiang fauna, is interpreted as a chordate and possibly a craniate, as it shows signs of a heart, arteries, gill filaments, a tail, a neural chord with a brain at the front end, and possibly eyes — although it also had short tentacles round its mouth. Haikouichthys and Myllokunmingia, also from the Chengjiang fauna, are regarded as fish. Pikaia, discovered much earlier but from the Mid Cambrian Burgess Shale, is also regarded as a primitive chordate.
On the other hand, fossils of early chordates are very rare, as non-vertebrate chordates have no bone tissue or teeth, and fossils of no Post-Cambrian non-vertebrate chordates are known aside from the Permian-aged Paleobranchiostoma, trace fossils of the Ordovician colonial tunicate Catellocaula, and various Jurassic-aged and Tertiary-aged spicules tentatively attributed to ascidians.

Phylogeny

Below is a phylogenetic tree showing consensus relationships among deuterostome taxa. Phylogenomic evidence suggests the enteropneust family, Torquaratoridae, fall within the Ptychoderidae. The tree is based on 16S +18S rRNA sequence data and phylogenomic studies from multiple sources. The approximate dates for each radiation into a new clade are given in millions of years ago. Not all dates are consistent, as of date ranges only the center is given.
Deuterostomes support is not unequivocal. In particular, Ambulacraria appears to be related to the Xenacoelomorpha, normally considered sister to Nephrozoa. If held up, possibilities are that the Ambulacraria are taken out of the Deutostomes and Nephrozoa, in which case the Deuterostomes grouping dissolves, or that the Xenacoelopomorpha are re-positioned next to the Ambulacraria, within the Deuterostomes.