Abstract

BackgroundMale song sparrows (Melospiza melodia) are territorial year-round; however, neuroendocrine responses to simulated territorial intrusion (STI) differ between breeding (spring) and non-breeding seasons (autumn). In spring, exposure to STI leads to increases in luteinizing hormone and testosterone, but not in autumn. These observations suggest that there are fundamental differences in the mechanisms driving neuroendocrine responses to STI between seasons. Microarrays, spotted with EST cDNA clones of zebra finch, were used to explore gene expression profiles in the hypothalamus after territorial aggression in two different seasons.Methodology/Principal FindingsFree-living territorial male song sparrows were exposed to either conspecific or heterospecific (control) males in an STI in spring and autumn. Behavioral data were recorded, whole hypothalami were collected, and microarray hybridizations were performed. Quantitative PCR was performed for validation. Our results show 262 cDNAs were differentially expressed between spring and autumn in the control birds. There were 173 cDNAs significantly affected by STI in autumn; however, only 67 were significantly affected by STI in spring. There were 88 cDNAs that showed significant interactions in both season and STI.Conclusions/SignificanceResults suggest that STI drives differential genomic responses in the hypothalamus in the spring vs. autumn. The number of cDNAs differentially expressed in relation to season was greater than in relation to social interactions, suggesting major underlying seasonal effects in the hypothalamus which may determine the differential response upon social interaction. Functional pathway analyses implicated genes that regulate thyroid hormone action and neuroplasticity as targets of this neuroendocrine regulation.

Highlights

  • Testosterone (T) has classically been regarded as a major factor in the control of vertebrate aggression, at least in reproductive contexts

  • An simulated territorial intrusion (STI) increased the number of songs by 2.2-fold (SE, 2566.0 songs; SC, 11.362.4 songs; U(8,8) = 52.5, p,0.05) and the number of flights by 9.3-fold (SE, 46.564.3 flights; SC, 560.9 flights; U(8,8) = 64, p,0.01), compared to controls

  • There was decrease in the basal number of songs compared to spring (AC; 261.6 songs; U(8,8) = 54, p,0.05 vs. SC) but birds still responded robustly to STI with a 12.5 fold increase (AE; 2566.9 songs) compared to controls (U(8,8) = 61, p,0.01, AE vs. AC)

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Summary

Introduction

Testosterone (T) has classically been regarded as a major factor in the control of vertebrate aggression, at least in reproductive contexts. The ‘‘challenge hypothesis’’ [5] attempts to explain the variable linkage of T and aggression during the breeding season. It suggests that a correlation between the two exists only during social instability, such as during establishment of dominance relationships and/or territorial boundaries, or when animals are ‘‘challenged’’ by a conspecific male for their territories and/or mates. Exposure to STI leads to increases in luteinizing hormone and testosterone, but not in autumn. These observations suggest that there are fundamental differences in the mechanisms driving neuroendocrine responses to STI between seasons. Microarrays, spotted with EST cDNA clones of zebra finch, were used to explore gene expression profiles in the hypothalamus after territorial aggression in two different seasons

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