DSpace
 
  Repositório Institucional da Universidade de Aveiro > Departamento de Biologia > BIO - Artigos >
 Nickel response in function of temperature differences: Effects at different levels of biological organization in Daphnia magna
Please use this identifier to cite or link to this item http://hdl.handle.net/10773/6618

title: Nickel response in function of temperature differences: Effects at different levels of biological organization in Daphnia magna
authors: Vandenbrouck, T
Dom, N
Novais, S
Soetaert, A
Ferreira, ALG
Loureiro, S
Soares, AMVM
De Coen, W
keywords: Daphnia magna
Life-history traits
Microarray
Mode of action (MOA)
Multiple stressors
Nickel
Temperature
issue date: 2011
publisher: Elsevier
abstract: In this study, gene transcription profiling in combination with the assessment of systemic parameters at individual and population levels were applied to study the (toxic) effects induced through temperature stress in the presence or the absence of an additional chemical stressor (nickel) in Daphnia magna. It was illustrated that lower temperatures were mainly characterized by a reduction of growth and lipid content, while higher temperatures caused an increase of both endpoints. Many of the differentially regulated transcripts could be correlated with processes affected at higher hierarchical levels of biological organization. Gene clusters with probable roles in producing offspring (peak expression at 22 degrees C), enhancing the metabolic rate (temperature related expression) and translational processes (increased expression at 14 degrees C) were identified. However, it was not possible to pinpoint a specific subset of genes, exclusively responding to temperature or nickel and allowing a retrospective identification of the particular stressor. Overall, extreme temperatures caused a higher level of stress in the organisms in comparison to nickel exposure. Moreover, organisms subjected to the natural stressor appeared to be less capable of dealing with the additional chemical stressor and as a result activate or repress more gene pathways. (C) 2011 Elsevier Inc. All rights reserved.
URI: http://hdl.handle.net/10773/6618
ISSN: 1744-117X
publisher version/DOI: http://dx.doi.org/10.1016/j.cbd.2011.06.001
source: Comparative Biochemistry and Physiology - Part D: Genomics and Proteomics
appears in collectionsBIO - Artigos

files in this item

file description sizeformat
248_CBP_2011_6D_271.pdf1.53 MBAdobe PDFview/open
Restrict Access. You can Request a copy!
statistics

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! RCAAP OpenAIRE DeGóis
ria-repositorio@ua.pt - Copyright ©   Universidade de Aveiro - RIA Statistics - Powered by MIT's DSpace software, Version 1.6.2