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Plzf mediates transcriptional repression of HoxD gene expression through chromatin remodeling.

作者信息

Barna Maria, Merghoub Taha, Costoya José A, Ruggero Davide, Branford Matthew, Bergia Anna, Samori Bruno, Pandolfi Pier Paolo

机构信息

Molecular Biology Program, Department of Pathology, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Dev Cell. 2002 Oct;3(4):499-510. doi: 10.1016/s1534-5807(02)00289-7.

Abstract

The molecular mechanisms that regulate coordinated and colinear activation of Hox gene expression in space and time remain poorly understood. Here we demonstrate that Plzf regulates the spatial expression of the AbdB HoxD gene complex by binding to regulatory elements required for restricted Hox gene expression and can recruit histone deacetylases to these sites. We show by scanning forced microscopy that Plzf, via homodimerization, can form DNA loops and bridge distant Plzf binding sites located within HoxD gene regulatory elements. Furthermore, we demonstrate that Plzf physically interacts with Polycomb proteins on DNA. We propose a model by which the balance between activating morphogenic signals and transcriptional repressors such as Plzf establishes proper Hox gene expression boundaries in the limb bud.

摘要

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