Source:http://linkedlifedata.com/resource/pubmed/id/21483679
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| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
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| pubmed:dateCreated |
2011-4-12
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| pubmed:abstractText |
Theoretical and empirical studies have sought to explain the formation and maintenance of social relationships within groups. The resulting dominance hierarchies have significant fitness and survival consequences dependent upon social status. We hypothesised that each position or rank within a group has a distinctive brain gene expression profile that correlates with behavioural phenotype. Furthermore, transitions in rank position should determine which genes shift in expression concurrent with the new dominance status. We used a custom cDNA microarray to profile brain transcript expression in a model species, the rainbow trout, which forms tractable linear hierarchies. Dominant, subdominant and submissive individuals had distinctive transcript profiles with 110 gene probes identified using conservative statistical analyses. By removing the dominant, we characterised the changes in transcript expression in sub-dominant individuals that became dominant demonstrating that the molecular transition occurred within 48 hours. A strong, novel candidate gene, ependymin, which was highly expressed in both the transcript and protein in subdominants relative to dominants, was tested further. Using antibody injection to inactivate ependymin in pairs of dominant and subdominant zebrafish, the subdominant fish exhibited a substantial increase in aggression in parallel with an enhanced competitive ability. This is the first study to characterise the molecular signatures of dominance status within groups and the first to implicate ependymin in control of aggressive behaviour. It also provides evidence for indirect genetic effect models in which genotype/phenotype of an individual is influenced by conspecific interactions within a group. The variation in the molecular profile of each individual within a group may offer a new explanation of intraspecific variation in gene expression within undefined groups of animals and provides new candidates for empirical study.
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| pubmed:commentsCorrections |
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:issn |
1932-6203
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:volume |
6
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
e18181
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| pubmed:dateRevised |
2011-7-28
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| pubmed:meshHeading |
pubmed-meshheading:21483679-Aggression,
pubmed-meshheading:21483679-Animals,
pubmed-meshheading:21483679-Brain,
pubmed-meshheading:21483679-Gene Expression Profiling,
pubmed-meshheading:21483679-Male,
pubmed-meshheading:21483679-Nerve Tissue Proteins,
pubmed-meshheading:21483679-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:21483679-Oncorhynchus mykiss,
pubmed-meshheading:21483679-Social Dominance,
pubmed-meshheading:21483679-Zebrafish,
pubmed-meshheading:21483679-Zebrafish Proteins
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| pubmed:year |
2011
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| pubmed:articleTitle |
Molecular correlates of social dominance: a novel role for ependymin in aggression.
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| pubmed:affiliation |
Institute of Integrative Biology and Centre for Genomic Research, University of Liverpool, Liverpool, United Kingdom. lsneddon@liverpool.ac.uk
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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