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Krüppel-like zinc finger transcription factors compose the largest transcription factor family in the mammalian genome. However, the functions for the majority of these transcription factors as well as their in vivo downstream targets are not clear. We have functionally characterized a novel KRAB domain zinc finger transcription factor ZNF431 using both in vitro and in vivo assays. ZNF431 is a nuclear transcriptional repressor whose repressive activity depends on its association with HDAC1 and -2. Using the limbmesenchymal cell line MPLB, we identified Patched1 as a direct transcriptional target of ZNF431. Promoter analyses revealed three ZNF431 binding sites that bind to ZNF431 both in vitro and in vivo as revealed by gel-shift and chromatin immunoprecipitation, respectively. Mutations of these three sites abolished ZNF431 repression in transient transfection assays. Moreover, overexpressing ZNF431 in MPLB cells or in Xenopus and mouse embryos strongly repressed Patched1 expression. On the other hand, shRNA knockdown of ZNF431 in MPLB cells elevated Patched1 expression. Finally, hedgehog signaling readout was reduced in ZNF431 overexpression but elevated in ZNF431 knockdown MPLB cells. Our results indicate that ZNF431 directly represses Patched1 expression and likely functions to repress the hedgehog response in cells.
FIGURE 6. Overexpression of ZNF431 repressed Ptch1 expression in Xenopus
and transgenic mouse embryos. A, shown are whole mount in situ
hybridization results of Xptc1 expression. The injected halves (Inj.) are indicated
by X-gal staining. B, a schematic diagram of the ZNF431 transgene is
shown. HA-tagged ZNF431 was driven by the chicken -actin promoter
preceded by a LoxP-flanked transcriptional stop cassette and a -globin
intron. The relative positions of genotyping primers are indicated by arrows.
C, whole mount in situ hybridization of Ptch1 expression in E10.5 wild-type
(upper) or HA-ZNF431 transgenic embryos (lower) is show. Ptch1 staining in
the limb bud is indicated by arrows. D, real-time PCR quantification of Ptch1
expression in wild-type or HA-ZNF431 transgenic embryos is shown. The
results were shown as relative Ptch1 expression. Tg, transgenic.
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