4.7 Article

Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development

期刊

GENES & DEVELOPMENT
卷 17, 期 3, 页码 368-379

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.1059403

关键词

Six3; forebrain; mouse; homeobox; Wnt; zebrafish

资金

  1. NCI NIH HHS [CA-21765, P30 CA021765] Funding Source: Medline
  2. NEI NIH HHS [EY12162, R01 EY012162] Funding Source: Medline
  3. NIGMS NIH HHS [R01 GM058462, GM58462] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS052386] Funding Source: Medline

向作者/读者索取更多资源

In vertebrate embryos, formation of anterior neural structures requires suppression of Wnt signals emanating from the paraxial mesoderm and midbrain territory. In Six3(-/-) mice, the prosencephalon was severely truncated, and the expression of Wnt1 was rostrally expanded, a finding that indicates that the mutant head was posteriorized. Ectopic expression of Six3 in chick and fish embryos, together with the use of in vivo and in vitro DNA-binding assays, allowed us to determine that Six3 is a direct negative regulator of Wnt1 expression. These results, together with those of phenotypic rescue of headless/tcf3 zebrafish mutants by mouse Six3, demonstrate that regionalization of the vertebrate forebrain involves repression of Wnt1 expression by Six3 within the anterior neuroectoderm. Furthermore, these results support the hypothesis that a Wnt signal gradient specifies posterior fates in the anterior neural plate.

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