๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Development and evolution of chordate cartilage

โœ Scribed by Amanda L. Rychel; Billie J. Swalla


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
410 KB
Volume
308B
Category
Article
ISSN
1552-5007

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

Deuterostomes are a monophyletic group of animals containing vertebrates, lancelets, tunicates, hemichordates, echinoderms, and xenoturbellids. Four out of these six extant groupsโ€”vertebrates, lancelets, tunicates, and hemichordatesโ€”have pharyngeal gill slits. All groups of deuterostome animals that have pharyngeal gill slits also have a pharyngeal skeleton supporting the pharyngeal openings, except tunicates. We previously found that pharyngeal cartilage in hemichordates and cephalochordates contains a fibrillar collagen protein similar to vertebrate type II collagen, but unlike vertebrate cartilage, the invertebrate deuterostome cartilages are acellular. We found SoxE and fibrillar collagen expression in the pharyngeal endodermal cells adjacent to where the cartilages form. These same endodermal epithelial cells also express Pax1/9, a marker of pharyngeal endoderm in vertebrates, lancelets, tunicates, and hemichordates. In situ experiments with a cephalochordate fibrillar collagen also showed expression in pharyngeal endoderm, as well as the ectoderm and the mesodermal coelomic pouches lining the gill bars. These results indicate that the pharyngeal endodermal cells are responsible for secretion of the cartilage in hemichordates, whereas in lancelets, all the pharyngeal cells surrounding the gill bars, ectodermal, endodermal, and mesodermal may be responsible for cartilage formation. We propose that endoderm secretion was primarily the ancestral mode of making pharyngeal cartilages in deuterostomes. Later the evolutionary origin of neural crest allowed coโ€option of the gene network for the secretion of pharyngeal cartilage matrix in the new migratory neural crest cell populations found in vertebrates. J. Exp. Zool. (Mol. Dev. Evol.) 308B:325โ€“335, 2007. ยฉ 2007 Wileyโ€Liss, Inc.


๐Ÿ“œ SIMILAR VOLUMES


Chordate origins and evolution
โœ Billie J. Swalla; Josรฉ Xavier-Neto ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 71 KB
New developments in vertebrate cytotaxon
โœ D. Colombera ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Springer Netherlands ๐ŸŒ English โš– 292 KB

A correlation between evolutionary trends and karyotype has been recognized in tunicates. In the ambit of lower chordates and related species, Hemichordata, Cephalochordata and, in the Tunicata, some ascidians seem to maintain a primitive organization of chromosomes: haploid numbers around 20, absen

Evolution of the chordate muscle actin g
โœ Subha Kovilur; James W. Jacobson; Rebecca L. Beach; William R. Jeffery; Craig R. ๐Ÿ“‚ Article ๐Ÿ“… 1993 ๐Ÿ› Springer ๐ŸŒ English โš– 763 KB

The ascidians Styela plicata, S. clava, and Mogula citrina are urochordates. The larvae of urochordates are considered to morphologically resemble the ancestral vertebrate. We asked whether larval and adult ascidian muscle actin sequences are nonmusclelike as in lower invertebrates, musclelike as in