Literature DB >> 17270396

Neuroanatomical specificity of sex differences in expression of aromatase mRNA in the quail brain.

Cornelia Voigt1, Gregory F Ball, Jacques Balthazart.   

Abstract

In birds and mammals, aromatase activity in the preoptic-hypothalamic region (HPOA) is usually higher in males than in females. It is, however, not known whether the enzymatic sex difference reflects the differential activation of aromatase transcription or some other control mechanism. Although sex differences in aromatase activity are clearly documented in the HPOA of Japanese quail (Coturnix japonica), only minimal or even no differences at all were observed in the number of aromatase-immunoreactive (ARO-ir) cells in the medial preoptic nucleus (POM) and in the medial part of the bed nucleus striae terminalis (BSTM). We investigated by in situ hybridization the distribution and possible sex differences in aromatase mRNA expression in the brain of sexually active adult quail. The distribution of aromatase mRNA matched very closely the results of previous immunocytochemical studies with the densest signal being observed in the POM, BSTM and in the mediobasal hypothalamus (MBH). Additional weaker signals were detected in the rostral forebrain, arcopallium and mesencephalic regions. No sex difference in the optical density of the hybridization signal could be found in the POM and MBH but the area covered by mRNA was larger in males than in females, indicating a higher overall expression in males. In contrast, in the BSTM, similar areas were covered by the aromatase expression in both sexes but the density of the signal was higher in females than in males. The physiological control of aromatase is thus neuroanatomically specific and with regard to sex differences, these controls are at least partially different if one compares the level of transcription, translation and activity of the enzyme. These results also indirectly suggest that the sex difference in aromatase enzyme activity that is present in the quail HPOA largely results from differentiated controls of enzymatic activity rather than differences in enzyme concentration.

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Year:  2007        PMID: 17270396     DOI: 10.1016/j.jchemneu.2006.12.004

Source DB:  PubMed          Journal:  J Chem Neuroanat        ISSN: 0891-0618            Impact factor:   3.052


  20 in total

1.  Birth of neural progenitors during the embryonic period of sexual differentiation in the Japanese quail brain.

Authors:  Sylvia M Bardet; Karen Mouriec; Jacques Balthazart
Journal:  J Comp Neurol       Date:  2012-12-15       Impact factor: 3.215

Review 2.  On the role of brain aromatase in females: why are estrogens produced locally when they are available systemically?

Authors:  Charlotte A Cornil
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2017-10-30       Impact factor: 1.836

3.  Sexually differentiated and neuroanatomically specific co-expression of aromatase neurons and GAD67 in the male and female quail brain.

Authors:  Charlotte A Cornil; Gregory F Ball; Jacques Balthazart
Journal:  Eur J Neurosci       Date:  2020-06-10       Impact factor: 3.386

4.  Neuroendocrine correlates of sex-role reversal in barred buttonquails.

Authors:  Cornelia Voigt
Journal:  Proc Biol Sci       Date:  2016-11-30       Impact factor: 5.349

5.  Glucocorticoid-induction of hypothalamic aromatase via its brain-specific promoter.

Authors:  D C Brooks; H Zhao; M B Yilmaz; J S Coon V; S E Bulun
Journal:  Mol Cell Endocrinol       Date:  2012-06-13       Impact factor: 4.102

6.  Sex differences in the rapid control of aromatase activity in the quail preoptic area.

Authors:  A T M Konkle; J Balthazart
Journal:  J Neuroendocrinol       Date:  2011-05       Impact factor: 3.627

7.  Aromatase promoter I.f is regulated by progesterone receptor in mouse hypothalamic neuronal cell lines.

Authors:  M Bertan Yilmaz; Andrew Wolfe; Hong Zhao; David C Brooks; Serdar E Bulun
Journal:  J Mol Endocrinol       Date:  2011-07-18       Impact factor: 5.098

8.  Sex differences in the expression of sex steroid receptor mRNA in the quail brain.

Authors:  C Voigt; G F Ball; J Balthazart
Journal:  J Neuroendocrinol       Date:  2009-10-20       Impact factor: 3.627

9.  Expression of reelin, its receptors and its intracellular signaling protein, Disabled1 in the canary brain: relationships with the song control system.

Authors:  J Balthazart; C Voigt; G Boseret; G F Ball
Journal:  Neuroscience       Date:  2008-02-21       Impact factor: 3.590

10.  Rapid control of male typical behaviors by brain-derived estrogens.

Authors:  Charlotte A Cornil; Gregory F Ball; Jacques Balthazart
Journal:  Front Neuroendocrinol       Date:  2012-09-13       Impact factor: 8.606

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