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Genome-wide distribution of linker histone H1.0 is independent of MeCP2.
Ito-Ishida, Aya; Yamalanchili, Hari Krishna; Shao, Yingyao; Baker, Steven A; Heckman, Laura D; Lavery, Laura A; Kim, Ji-Yoen; Lombardi, Laura M; Sun, Yaling; Liu, Zhandong; Zoghbi, Huda Y.
Afiliación
  • Ito-Ishida A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Yamalanchili HK; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
  • Shao Y; Department of Physiology, Keio University School of Medicine, Tokyo, Japan.
  • Baker SA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Heckman LD; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
  • Lavery LA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Kim JY; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
  • Lombardi LM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Sun Y; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
  • Liu Z; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Zoghbi HY; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, TX, USA.
Nat Neurosci ; 21(6): 794-798, 2018 06.
Article en En | MEDLINE | ID: mdl-29802390
ABSTRACT
Previous studies suggested that MeCP2 competes with linker histone H1, but this hypothesis has never been tested in vivo. Here, we performed chromatin immunoprecipitation followed by sequencing (ChIP-seq) of Flag-tagged-H1.0 in mouse forebrain excitatory neurons. Unexpectedly, Flag-H1.0 and MeCP2 occupied similar genomic regions and the Flag-H1.0 binding was not changed upon MeCP2 depletion. Furthermore, mild overexpression of H1.0 did not alter MeCP2 binding, suggesting that the functional binding of MeCP2 and H1.0 are largely independent.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Histonas / Proteína 2 de Unión a Metil-CpG Idioma: En Revista: Nat Neurosci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Histonas / Proteína 2 de Unión a Metil-CpG Idioma: En Revista: Nat Neurosci Asunto de la revista: NEUROLOGIA Año: 2018 Tipo del documento: Article