Inhibition of SRY-Calmodulin Complex Formation Induces Ectopic Expression of Ovarian Cell Markers in Developing XY Gonads

Autor: Francis Poulat, Daniel Peter Czech, Peter Koopman, Anthony Argentaro, Andrew H. Sinclair, Vincent R. Harley, Helena Sim, Stefan Bagheri-Fam, Brigitte Boizet-Bonhoure
Přispěvatelé: Institut de génétique humaine (IGH), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Forkhead Box Protein L2
Male
Mice
0302 clinical medicine
Endocrinology
Chlorocebus aethiops
Testis
ComputingMilieux_MISCELLANEOUS
Spermatic Cord
0303 health sciences
Sexual differentiation in humans
Forkhead Transcription Factors
SOX9 Transcription Factor
Recombinant Proteins
Forkhead box L2
medicine.anatomical_structure
Testis determining factor
COS Cells
geographic locations
Transcriptional Activation
endocrine system
medicine.medical_specialty
animal structures
Gonad
Active Transport
Cell Nucleus

SOX9
Biology
Y chromosome
03 medical and health sciences
Organ Culture Techniques
Calmodulin
Internal medicine
parasitic diseases
medicine
Animals
Spermatogenesis
Transcription factor
030304 developmental biology
Cell Nucleus
[SDV.GEN]Life Sciences [q-bio]/Genetics
social sciences
Sex Determination Processes
Embryo
Mammalian

Antigens
Differentiation

Sex-Determining Region Y Protein
Calmodulin-Binding Proteins
Ectopic expression
Thrombospondins
030217 neurology & neurosurgery
Zdroj: Endocrinology
Endocrinology, Endocrine Society, 2011, 152 (7), pp.2883-2893. ⟨10.1210/en.2010-1475⟩
ISSN: 0013-7227
DOI: 10.1210/en.2010-1475⟩
Popis: The transcription factor sex-determining region of the Y chromosome (SRY) plays a key role in human sex determination, because mutations in SRY cause disorders of sex development in XY individuals. During gonadal development, Sry in pre-Sertoli cells activates Sox9 gene transcription, committing the fate of the bipotential gonad to become a testis rather than an ovary. The high-mobility group domain of human SRY contains two independent nuclear localization signals, one bound by calmodulin (CaM) and the other by importin-β. Although XY females carry SRY mutations in these nuclear localization signals that affect SRY nuclear import in transfected cells, it is not known whether these transport mechanisms are essential for gonadal development and sex determination. Here, we show that mouse Sry protein binds CaM and that a CaM antagonist reduces CaM binding, nuclear accumulation, and transcriptional activity of Sry in transfected cells. CaM antagonist treatment of cultured, sexually indifferent XY mouse fetal gonads led to reduced expression of the Sry target gene Sox9, defects in testicular cord formation, and ectopic expression of the ovarian markers Rspondin1 and forkhead box L2. These results indicate the importance of CaM for SRY nuclear import, transcriptional activity, testis differentiation, and sex determination.
Databáze: OpenAIRE