Cargando…
Genome Wide Distribution of Linker Histone H1.0 is Independent of MeCP2
Previous studies suggested that MeCP2 competes with linker histone H1, but this hypothesis has never been tested in vivo. Here, we performed 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 bindin...
Autores principales: | Ito-Ishida, Aya, Yamalanchili, Hari K., Shao, Yingyao, Baker, Steven A., Heckman, Laura D., Lavery, Laura A., Kim, Ji-yoen, Lombardi, Laura M., Sun, Yaling, Liu, Zhandong, Zoghbi, Huda Y. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099063/ https://www.ncbi.nlm.nih.gov/pubmed/29802390 http://dx.doi.org/10.1038/s41593-018-0155-8 |
Ejemplares similares
-
Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice
por: Heckman, Laura Dean, et al.
Publicado: (2014) -
Apparent bias toward long gene misregulation in MeCP2 syndromes disappears after controlling for baseline variations
por: Raman, Ayush T., et al.
Publicado: (2018) -
Genetic Modifiers of MeCP2 Function in Drosophila
por: Cukier, Holly N., et al.
Publicado: (2008) -
Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders
por: Zhou, Jian, et al.
Publicado: (2022) -
MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function
por: Bajikar, Sameer S, et al.
Publicado: (2023)