Grant: Discovery Grants Program - Individual
Université de Moncton
$33,000.00
Sox transcription factors: Regulatory mechanisms and impact on steroidogenesis
EF 2014-15
Résumé
Members of the Sox family of transcription factors, Sry and Sox9, are known to play important roles in sex determination and differentiation in mammals. More than 20 members of this family have been characterized, of which several are expressed in the testis. To ensure their specificity of action, Sox proteins rely on recruitment of partners and post-translational modifications. However, their role in transcriptional regulation of steroidogenesis has never been investigated. Interestingly, putative binding sites for Sox members are present in the promoters of several steroidogenic genes. Thus, Sox family members might play a crucial role in transcriptional regulation of steroidogenesis in Leydig cells. These cells supply testosterone important to maintain fertility in male and to avoid andropause related symptoms associated to aging. Steroidogenesis can be regulated at different levels such as gonads (for steroidogenic genes), pituitary (by regulating LH and FSH productions) and hypothalamus (by regulating GnRH production). Therefore, the main goal of my research program is to define the role of Sox members in functional regulation of the Hypothalamic-Pituitary-Gonadal axis, important for sex steroids production. The current proposal aims to identify which Sox members are expressed in rodent male gonads, which genes they regulate and what mechanisms regulate their activities. Overall, different approaches of molecular and cell biology will be used to better understand the role of Sox transcription factors in Leydig cells' function. As in other tissues, Sox members might be functionally redundant in steroidogenic cells, explaining the lack of steroidogenic phenotypes in Sox-deficient mice models. Results from this proposal will have a great significance for basic physiology and endocrinology of gonadal steroidogenesis in vertebrates and might be relevant for novel male contraception. In addition, our results will contribute to a better understanding of prostate cancer development and progression.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
New Brunswick, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
386557-2012
Name nom
Martin, Luc
Department département
Biologie
Organization id
73
Institution établissement
Université de Moncton
Province en
New Brunswick
Province fr
Nouveau-Brunswick
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2012
Award amount
33000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5303
Research subject group en
Molecular biology
Research subject group fr
Biologie moléculaire
Research subject en
Gene regulation
Research subject fr
Régulation des gènes
Partie
3
Nb partie
5
Application title
Sox transcription factors: Regulatory mechanisms and impact on steroidogenesis
Keyword
NSERC
Application summary
Members of the Sox family of transcription factors, Sry and Sox9, are known to play important roles in sex determination and differentiation in mammals. More than 20 members of this family have been characterized, of which several are expressed in the testis. To ensure their specificity of action, Sox proteins rely on recruitment of partners and post-translational modifications. However, their role in transcriptional regulation of steroidogenesis has never been investigated. Interestingly, putative binding sites for Sox members are present in the promoters of several steroidogenic genes. Thus, Sox family members might play a crucial role in transcriptional regulation of steroidogenesis in Leydig cells. These cells supply testosterone important to maintain fertility in male and to avoid andropause related symptoms associated to aging. Steroidogenesis can be regulated at different levels such as gonads (for steroidogenic genes), pituitary (by regulating LH and FSH productions) and hypothalamus (by regulating GnRH production). Therefore, the main goal of my research program is to define the role of Sox members in functional regulation of the Hypothalamic-Pituitary-Gonadal axis, important for sex steroids production. The current proposal aims to identify which Sox members are expressed in rodent male gonads, which genes they regulate and what mechanisms regulate their activities. Overall, different approaches of molecular and cell biology will be used to better understand the role of Sox transcription factors in Leydig cells' function. As in other tissues, Sox members might be functionally redundant in steroidogenic cells, explaining the lack of steroidogenic phenotypes in Sox-deficient mice models. Results from this proposal will have a great significance for basic physiology and endocrinology of gonadal steroidogenesis in vertebrates and might be relevant for novel male contraception. In addition, our results will contribute to a better understanding of prostate cancer development and progression.