scholarly journals Computational Study of Evolutionary Selection Pressure on Rainbow Trout Estrogen Receptors

PLoS ONE ◽  
2010 ◽  
Vol 5 (3) ◽  
pp. e9392 ◽  
Author(s):  
Conrad Shyu ◽  
Celeste J. Brown ◽  
F. Marty Ytreberg
2010 ◽  
Vol 120 (1) ◽  
pp. 42-58 ◽  
Author(s):  
Abby D. Benninghoff ◽  
William H. Bisson ◽  
Daniel C. Koch ◽  
David J. Ehresman ◽  
Siva K. Kolluri ◽  
...  

2002 ◽  
Vol 10 (4) ◽  
pp. 437-454 ◽  
Author(s):  
James Serpell

AbstractThis article explores the origin and evolutionary implications of anthropomorphism in the context of our relationships with animal companions. On the human side, anthropomorphic thinking enables animal companions' social behavior to be construed in human terms, thereby allowing these nonhuman animals to function for their human owners or guardians as providers of nonhuman social support. Absence of social support is known to be detrimental to human health and well being. Therefore, anthropomorphism and its corollary, pet keeping, have obvious biological fitness implications. On the animal side, anthropomorphism constitutes a unique evolutionary selection pressure, analogous to sexual selection, which has molded the appearance, anatomy, and behavior of companion animal species so as to adapt them to their unusual ecological niche as social support providers. Although such species undoubtedly have benefited numerically from the effects of this process, the consequences of anthropomorphism are less benign when viewed from the perspective of individual animals. Indeed, anthropomorphic selection probably is responsible for some of the more severe welfare problems currently found in companion animals.


Author(s):  
A. Nakayama ◽  
E. Oldenberg ◽  
E. Eppler ◽  
B. Köllner ◽  
H. Segner

Gene ◽  
2013 ◽  
Vol 531 (2) ◽  
pp. 403-410 ◽  
Author(s):  
Baojun Wu ◽  
Jing Gong ◽  
Shoudao Yuan ◽  
Ying Zhang ◽  
Tiandi Wei

2019 ◽  
Vol 18 (11) ◽  
pp. 1508-1520 ◽  
Author(s):  
M. Martinez-Archundia ◽  
J.B. García-Vázquez ◽  
B. Colin-Astudillo ◽  
M. Bello ◽  
B. Prestegui-Martel ◽  
...  

Estrogen (17β-estradiol) is essential for normal growth and differentiation in the mammary gland. In the last three decades, previous investigations have revealed that Estrogen Receptor Alpha (ERα) plays a critical role in breast cancer. More recently, observations regarding the widespread expression of ERβ-like proteins in normal and neoplastic mammary tissues have suggested that ERβ is also involved in the mentioned pathology. Design of new drugs both steroidal and nonsteroidal that target any of these receptors represents a promise to treat breast cancer although it remains a challenge due to the sequence similarity between their catalytic domains. In this work, we propose a new set of compounds that could effectively target the estrogen receptors ERα and ERβ. These ligands were designed based on the chemical structure of the ERβ-selective agonist Diarylpropionitrile (DPN). The designed ligands were submitted to in silico ADMET studies, yielding in a filtered list of ligands that showed better drug-like properties. Molecular dynamics simulations of both estrogen receptors and docking analysis were carried-out employing the designed compounds, from which two were chosen due to their promising characteristics retrieved from theoretical results (docking analysis or targeting receptor predictions). They were chemically synthetized and during the process, two precursor ligands were also obtained. These four ligands were subjected to biological studies from which it could be detected that compound mol60b dislplayed inhibito


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