Estrogen Receptor Alpha as a Mediator of Life-History Trade-offs.
Estrogen Receptor Alpha as a Mediator of Life-History Trade-offs.
复制标题
雌激素受体α作为生活史权衡的中介。
DOI:
10.1093/icb/icv005
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发表时间:
2015
影响因子:
2.6
通讯作者:
Zinzow-Kramer,WendyM
中科院分区:
文献类型:
--
作者:
Maney,DonnaL;Horton,BrentM;Zinzow-Kramer,WendyM
Trade-offs between competitive and parental strategies often are mediated by sex steroids. The mechanisms underlying steroid signaling and metabolism may therefore serve as targets of disruptive selection that leads to alternative behavioral phenotypes. White-throated sparrows exhibit two color morphs that differ in both competitive and parental behavior; white-striped (WS) birds engage in more territorial singing, whereas tan-striped (TS) birds provision nestlings more often. Although WS birds have higher levels of plasma testosterone (T) and estradiol than do TS birds, experimental equalization of these hormones does not abolish morph differences in singing. Neural sensitivity to sex steroids may differ between the morphs because the gene for estrogen receptor alpha (ERα) has been captured by a chromosomal rearrangement found only in the WS birds. We recently showed that expression of this gene differs between the morphs and may drive the behavioral polymorphism. First, the ERα promoter region contains fixed polymorphisms that affect transcription efficiencyin vitro. Second, in a free-living population, local expression of ERα depends strongly on morph and predicts both territorial singing and parental provisioning. Differential ERα expression is particularly striking in the medial amygdala; WS birds have three times more ERα mRNA than do TS birds. This difference persists during the non-breeding season and is unaffected by exogenous T treatment. Finally, preliminary data generated by RNA-seq confirm that ERα expression in MeA is both differentially expressed and correlated with territorial singing. Together, these results suggest that ERα may be a target of disruptive selection that leads to alternative behavioral strategies. Our future directions include a more detailed analysis of the ERα promoter regions to determine the molecular basis of differential expression as well as gene network analyses to identify genes connected to ERα.
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DOI:
10.1002/neu.10225
发表时间:
2003
期刊:
Journal of neurobiology
影响因子:
--
作者:
Soma,KiranK;Schlinger,BarneyA;Wingfield,JohnC;Saldanha,ColinJ
通讯作者:
Saldanha,ColinJ
影响因子:
64.8
作者:
Wolf, Max;van Doorn, G. Sander;Weissing, Franz J.
通讯作者:
Weissing, Franz J.
影响因子:
2.6
作者:
Ketterson, Ellen D.;Atwell, Jonathan W.;McGlothlin, Joel W.
通讯作者:
McGlothlin, Joel W.
影响因子:
3.5
作者:
Fleming, AS;Corter, C;Steiner, M
通讯作者:
Steiner, M
DOI:
--
发表时间:
1988
期刊:
影响因子:
--
作者:
H. Schwabl;M. Ramenofsky;I. Schwabl;D. Farner;J. Wingfield
通讯作者:
J. Wingfield