4.6 Article

Developmental regulation of gonadotropin-releasing hormone gene expression by the MSX and DLX homeodomain protein families

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 280, 期 19, 页码 19156-19165

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M502004200

关键词

-

资金

  1. NICHD NIH HHS [R01 HD072754, P50 HD012303] Funding Source: Medline
  2. NIDA NIH HHS [T32 DA07315] Funding Source: Medline
  3. NIDDK NIH HHS [P30 DK063491, P30 DK063491-019001, R01 DK044838-16, R01 DK44838, R01 DK044838, R01 DK044838-17A1] Funding Source: Medline

向作者/读者索取更多资源

Gonadotropin-releasing hormone (GnRH) is the central regulator of the hypothalamic-pituitary-gonadal axis, controlling sexual maturation and fertility in diverse species from fish to humans. GnRH gene expression is limited to a discrete population of neurons that migrate through the nasal region into the hypothalamus during embryonic development. The GnRH regulatory region contains four conserved homeodomain binding sites (ATTA) that are essential for basal promoter activity and cell-specific expression of the GnRH gene. MSX and DLX are members of the Antennapedia class of non-Hox homeodomain transcription factors that regulate gene expression and influence development of the craniofacial structures and anterior forebrain. Here, we report that expression patterns of the Msx and Dlx families of homeodomain transcription factors largely coincide with the migratory route of GnRH neurons and co-express with GnRH in neurons during embryonic development. In addition, MSX and DLX family members bind directly to the ATTA consensus sequences and regulate transcriptional activity of the GnRH promoter. Finally, mice lacking MSX1 or DLX1 and 2 show altered numbers of GnRH-expressing cells in regions where these factors likely function. These findings strongly support a role for MSX and DLX in contributing to spatiotemporal regulation of GnRH transcription during development.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据