﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>International Journal of Evolutionary Biology</title><link>http://www.sage-hindawi.com</link><description>The latest articles from SAGE-Hindawi Access to Research</description><copyright>&amp;#169; 2010, SAGE-Hindawi Access to Research. All rights reserved.</copyright><item><title>Elucidating the Evolutionary Relationships among Bos taurus Digestive Organs Using Unigene Expression Data</title><link>http://www.sage-hindawi.com/journals/ijeb/2009/803142.html</link><description>Although the nature of ruminant evolution is still disputed, current theory based on physiology and genetic analysis suggests that the abomasum is the evolutionarily oldest stomach compartment, the rumen evolved some time after the abomasum, and the omasum is the evolutionarily youngest stomach compartment. In addition, there is some evidence of relaxed selective constraint in the stomach-like organ and the foregut shortly after the foregut formation event. Along with the assumption of a mean, stochastic rate of evolution, analysis of differences in genetic profiles among digestive body organs can give clues to the relationships among these organs. The presence of large numbers of uniquely expressed entries in the abomasum and rumen indicates either a period of relaxed selective constraint or greater evolutionary age. Additionally, differences in expression profiles indicate that the abomasum, rumen, and intestine are more closely related to each other, while the reticulum and omasum are more closely related to the rumen. Functional analysis using Gene Ontology (GO) categories also supports the proposed evolutionary relationships by identifying shared functions, such as muscle activity and development, lipid transport, and urea metabolism, between all sections of the digestive tract investigated.</description><Author>D. C. Beck, Honglin Jiang, and Liqing Zhang</Author><copyright>&amp;#169; 2010, SAGE-Hindawi Access to Research. All rights reserved.</copyright></item><item><title>Hormones and Sex-Specific Transcription Factors Jointly Control Yolk Protein Synthesis in Musca domestica</title><link>http://www.sage-hindawi.com/journals/ijeb/2009/291236.html</link><description>In the housefly Musca domestica, synthesis of yolk proteins (YPs) depends on the level of circulating ecdysteroid hormones. In female houseflies, the ecdysterone concentration in the hemolymph oscillates and, at high levels, is followed by expression of YP. In male houseflies, the ecdysterone titre is constantly low and no YP is produced. In some strains, which are mutant in key components of the sex-determining pathway, males express YP even though their ecdysterone titre is not significantly elevated. However, we find that these males express a substantial amount of the female variant of the Musca doublesex homologue, Md-dsx. The dsx gene is known to sex-specifically control transcription of yp genes in the fat body of Drosophila melanogaster. Our data suggest that Md-dsx also contributes to the regulation of YP expression in the housefly by modulating the responsiveness of YP-producing cells to hormonal stimuli.</description><Author>Christina Siegenthaler, Peter Maroy, Monika Hediger, Andreas D&amp;#252;bendorfer, and Daniel Bopp</Author><copyright>&amp;#169; 2010, SAGE-Hindawi Access to Research. All rights reserved.</copyright></item><item><title>Heritability of Directional Asymmetry in Drosophila melanogaster</title><link>http://www.sage-hindawi.com/journals/ijeb/2009/759159.html</link><description>Directional asymmetry (DA), the consistent difference between a pair of morphological structures in which the same side is always larger than the other, presents an evolutionary mystery. Although many paired traits show DA, genetic variation for DA has not been unambiguously demonstrated. Artificial selection is a powerful technique for uncovering selectable genetic variation; we review and critique the limited number of previous studies that have been performed to select on DA and present the results of a novel artificial selection experiment on the DA of posterior crossvein location in Drosophila wings. Fifteen generations of selection in two genetically distinct lines were performed and none of the lines showed a significant response to selection. Our results therefore support and reconfirm previous findings; despite apparent natural variation and evolution of DA in nature, DA remains a paradoxical trait that does not respond to artificial selection.</description><Author>Ashley J. R. Carter, Elizabeth Osborne, and David Houle</Author><copyright>&amp;#169; 2010, SAGE-Hindawi Access to Research. All rights reserved.</copyright></item><item><title>Divergence of AMP Deaminase in the Ice Worm Mesenchytraeus solifugus (Annelida, Clitellata, Enchytraeidae)</title><link>http://www.sage-hindawi.com/journals/ijeb/2009/715086.html</link><description>Glacier ice worms, Mesenchytraeus solifugus and related species, are the largest glacially obligate metazoans. As one component of cold temperature adaptation, ice worms maintain atypically high energy levels in an apparent mechanism to offset cold temperature-induced lethargy and death. To explore this observation at a mechanistic level, we considered the putative contribution of 5&amp;#x2032; adenosine monophosphate deaminase (AMPD), a key regulator of energy metabolism in eukaryotes. We cloned cDNAs encoding ice worm AMPD, generating a fragment encoding 543 amino acids that included a short N-terminal region and complete C-terminal catalytic domain. The predicted ice worm AMPD amino acid sequence displayed conservation with homologues from other mesophilic eukaryotes with notable exceptions. In particular, an ice worm-specific K188E substitution proximal to the AMP binding site likely alters the architecture of the active site and negatively affects the enzyme&amp;#39;s activity. Paradoxically, this would contribute to elevated intracellular ATP levels, which appears to be a signature of cold adapted taxa.</description><Author>Roberto Marotta, Bradley R. Parry, and Daniel H. Shain</Author><copyright>&amp;#169; 2010, SAGE-Hindawi Access to Research. All rights reserved.</copyright></item></channel></rss>