ID | 110703 |
著者 |
Chen, Gang
Department of Human Genetics and Public Health, Graduate School of Proteomics, Faculty of Medicine, The University of Tokushima|Core Research for Evolutional Science and Technology (CREST)
新家, 利一
Department of Human Genetics and Public Health, Graduate School of Proteomics, Faculty of Medicine, The University of Tokushima|Core Research for Evolutional Science and Technology (CREST)
キノシタ, ケイゴ
Department of Human Genetics and Public Health, Graduate School of Proteomics, Faculty of Medicine, The University of Tokushima|Core Research for Evolutional Science and Technology (CREST)
Yan, Hong-Tao
Department of Human Genetics and Public Health, Graduate School of Proteomics, Faculty of Medicine, The University of Tokushima|Core Research for Evolutional Science and Technology (CREST)
イワモト, テルアキ
Department of Urology, St.Marianna Medical University School of Medicine|Core Research for Evolutional Science and Technology (CREST)
中堀, 豊
Department of Human Genetics and Public Health, Graduate School of Proteomics, Faculty of Medicine, The University of Tokushima|Core Research for Evolutional Science and Technology (CREST)
|
キーワード | sex differentiation
MIS
promoter
estrogen
estrogen receptor
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資料タイプ |
学術雑誌論文
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抄録 | Sex differentiation consists of multi-step pathway that involves expression of many different genes. Müllerian duct inhibitory substance (MIS) has a key role for regression of the Müllerian duct during male sex differentiation. Recently, endocrine disruptors (EDs), which often have estrogen-like activities, have caused concern over worldwide. It has been reported that estrogen regulates the MIS expression. Therefore, we tested whether ERαand ERβinfluence the MIS promoter activity in the NT2/D1 cell line which expresses many sex differentiation related genes such as SRY, SOX9, and DAX-1. RT-PCR analysis revealed that the NT2/D1 cells express bother ERβ in addition to MIS. Under the low concentration of 17β-estradiol (E2), the over-expression of exogenous ERα increased the MIS promoter activity 3.3-fold compared with the control. However, as E2 concentration was increased, the MIS promoter activity was decreased. For ERβ, we could not observe alterations of the MIS promoter activity. Furthermore, the over-expression of the exogenous SF-1 inhibited the activation of the MIS promoter with ERα. Although it remains unclear whether the effects of ERαon the MIS promoter are mediated through the genomic or the no-genomic actions, the present results suggest that ERα upregulates the MIS promoter activity in the NT2/D1 cells under low concentrations of E2, and that the two ERs may work in different manners for the MIS promoter activation. The present findings may be useful to understand the molecular mechanisms by which EDs or estrogens affect the MIS expression.
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掲載誌名 |
The journal of medical investigation : JMI
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ISSN | 13431420
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cat書誌ID | AA11166929
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巻 | 50
|
号 | 3-4
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開始ページ | 192
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終了ページ | 198
|
並び順 | 192
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発行日 | 2003
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EDB ID | |
フルテキストファイル | |
言語 |
eng
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著者版フラグ |
出版社版
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