Abstract |
Loss of function mutations in SALL4 cause Okihiro syndrome, an autosomal dominant disorder characterised by radial ray malformations associated with Duane anomaly. In zebrafish and mouse Sall4 interacts with TBX5 during limb and heart development and plays a crucial role for embryonic stem (ES) cell pluripotency. Here we report the nuclear interaction of murine Sall4 with Cyclin D1, one of the main regulators of G(1) to S phase transition in cell cycle, verified by yeast two-hybrid assay, co-immunoprecipitation and intracellular co-localisation. Furthermore, using luciferase reporter gene assays we demonstrate that Sall4 operates as a transcriptional repressor located to heterochromatin and that this activity is modulated by Cyclin D1.
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Authors | Johann Böhm, Frank J Kaiser, Wiktor Borozdin, Reinhard Depping, Jürgen Kohlhase |
Journal | Biochemical and biophysical research communications
(Biochem Biophys Res Commun)
Vol. 356
Issue 3
Pg. 773-9
(May 11 2007)
ISSN: 0006-291X [Print] United States |
PMID | 17383611
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cyclin D
- Cyclins
- DNA-Binding Proteins
- Repressor Proteins
- Sall4 protein, mouse
- Transcription Factors
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Topics |
- Animals
- COS Cells
- Cell Nucleus
(metabolism)
- Chlorocebus aethiops
- Cyclin D
- Cyclins
(physiology)
- DNA-Binding Proteins
(physiology)
- Mice
- Repressor Proteins
(physiology)
- Transcription Factors
(physiology)
- Transcription, Genetic
(drug effects)
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