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Showing papers by "Huck-Hui Ng published in 2000"


Journal ArticleDOI
TL;DR: This work has shown that eukaryotic genes can be silenced by deacetylation of acetyl-lysine moieties in the N-terminal tails of histones, and links histoneDeacetylases with an increasing number of repressors, suggesting that deacetylene might be a rather pervasive feature of transcriptional repression systems.

470 citations


Journal ArticleDOI
TL;DR: The present study established by several experimental criteria that, contrary to a previous report, MBD1 is not a component of the MeCP1 repressor complex, and identified a powerful transcriptional repression domain (TRD) at the C terminus ofMBD1 that can actively repress transcription at a distance.
Abstract: MBD1 belongs to a family of mammalian proteins that share a methyl-CpG binding domain. Previous work has shown that MBD1 binds to methylated sites in vivo and in vitro and can repress transcription from methylated templates in transcription extracts and in cultured cells. In the present study we established by several experimental criteria that, contrary to a previous report, MBD1 is not a component of the MeCP1 repressor complex. We identified a powerful transcriptional repression domain (TRD) at the C terminus of MBD1 that can actively repress transcription at a distance. Methylation-dependent repression in vivo depends on the presence of both the TRD and the methyl-CpG binding domain. The mechanism is likely to involve deacetylation, since the deacetylase inhibitor trichostatin A can overcome MBD1-mediated repression. Accordingly, we found that endogenous MBD1 is particularly concentrated at sites of centromeric heterochromatin, where acetylated histone H4 is deficient. Unlike MBD2 and MeCP2, MBD1 is not depleted by antibodies to the histone deacetylase HDAC1. Thus, the deacetylase-dependent pathway by which MBD1 actively silences methylated genes is likely to be different from that utilized by the methylation-dependent repressors MeCP1 and MeCP2.

280 citations