𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Evidence on Mammalian Phylogeny from Sequences of Exon 28 of the von Willebrand Factor Gene

✍ Scribed by Calvin A. Porter; Morris Goodman; Michael J. Stanhope


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
574 KB
Volume
5
Category
Article
ISSN
1055-7903

No coin nor oath required. For personal study only.

✦ Synopsis


Phylogenetic relationships among 27 extant mammalian species (representing 15 placental orders) were studied using sequences of exon 28 of the gene encoding von Willebrand Factor (vWF), a glycoprotein which functions in blood clotting. Analysis of sequences coding for vWF revealed evidence for several subordinal and superordinal groupings, but the earliest branching sequence of placental mammals was left largely unresolved. Strong support was found for a monophyletic clade consisting of elephants, sea cows, hyraxes, aardvarks, and elephant shrews. This systematic placement of the elephant shrews agrees strongly with two other molecular data sets (interphotoreceptor retinoid binding protein and alpha-lens crystallins) and is consistent with analysis of fossil elephant shrews recently discovered in north Africa. Evidence from vWF sequences agrees with a number of previous molecular and morphological studies in providing strong support for the monophyly of both bats and rodents. The orders Primates, Proboscidea, Carnivora, Perissodactyla, and Artiodactyla were represented by more than one species which joined in each case to form a monophyletic order.


πŸ“œ SIMILAR VOLUMES


Higher-Level Phylogeny of the Therevidae
✍ Longlong Yang; Brian M. Wiegmann; David K. Yeates; Michael E. Irwin πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 English βš– 153 KB

Therevidae (stilleto flies) are a little-known family of asiloid brachyceran Diptera (Insecta). Separate and combined phylogenetic analyses of 1200 bases of the 28S ribosomal DNA and 1100 bases of elongation factor-1␣ were used to infer phylogenetic relationships within the family. The position of t

Search for mutations in a segment of the
✍ CasaΓ±a, Pilar; MartΓ­nez, Francisco; EspinΓ³s, Carmen; Haya, Saturnino; Lorenzo, J πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 431 KB πŸ‘ 1 views

von Willebrand Disease (vWD) is the most frequently inherited bleeding disorder in humans, and is caused by a qualitative and/or quantitative abnormality of the von Willebrand factor (vWF). A large number of defects that cause qualitative variants have been located in the A1 domain of the vWF, which