Endogenous expression of Müllerian inhibiting substance in early postnatal rat Sertoli cells requires multiple steroidogenic factor-1 and GATA-4-binding sites

التفاصيل البيبلوغرافية
العنوان: Endogenous expression of Müllerian inhibiting substance in early postnatal rat Sertoli cells requires multiple steroidogenic factor-1 and GATA-4-binding sites
المؤلفون: Patricia K. Donahoe, Xinzhong Wang, Trent R. Clarke, Koji Watanabe, Andrew H. Lane
بيانات النشر: The National Academy of Sciences, 2000.
سنة النشر: 2000
مصطلحات موضوعية: Steroidogenic factor 1, Anti-Mullerian Hormone, Male, Transcriptional Activation, Molecular Sequence Data, DNA Footprinting, Fushi Tarazu Transcription Factors, Receptors, Cytoplasmic and Nuclear, Biology, Steroidogenic Factor 1, Transfection, Adenoviridae, Genes, Reporter, medicine, otorhinolaryngologic diseases, Animals, Humans, RNA, Messenger, Promoter Regions, Genetic, Transcription factor, Glycoproteins, Regulation of gene expression, Homeodomain Proteins, Messenger RNA, Multidisciplinary, Binding Sites, Sertoli Cells, Base Sequence, Gene Expression Regulation, Developmental, Nuclear Proteins, Promoter, Biological Sciences, Sertoli cell, Molecular biology, Growth Inhibitors, GATA4 Transcription Factor, Rats, DNA-Binding Proteins, Testicular Hormones, medicine.anatomical_structure, Animals, Newborn, Regulatory sequence, Male sex differentiation, Transcription Factors
الوصف: Müllerian inhibiting substance (MIS) is a key element required to complete mammalian male sex differentiation. The expression pattern of MIS is tightly regulated in fetal, neonatal, and prepubertal testes and adult ovaries and is well conserved among mammalian species. Although several factors have been shown to be essential to MIS expression, its regulatory mechanisms are not fully understood. We have examined MIS promoter activity in 2-day postnatal primary cultures of rat Sertoli cells that continue to express endogenous MIS mRNA. Using this system, we found that the region between human MIS−269 and −192 is necessary for full MIS promoter activity. We identified by DNase I footprint and electrophoretic mobility-shift analyses a distal steroidogenic factor-1 (SF-1)-binding site that is essential for full promoter activity. Mutational analysis of this new distal SF-1 site and the previously identified proximal SF-1 site showed that both are necessary for transcriptional activation. Moreover, the proximal promoter also contains multiple GATA-4-binding sites that are essential for functional promoter activity. Thus multiple SF-1- and GATA-4-binding sites in the MIS promoter are required for normal tissue-specific and developmental expression of MIS.
اللغة: English
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de8453b5d06f9b52c374a387cf75e8a7Test
https://europepmc.org/articles/PMC26485Test/
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....de8453b5d06f9b52c374a387cf75e8a7
قاعدة البيانات: OpenAIRE