Cargando…

ORC1 BAH domain links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome

Recognition of distinctly modified histones by specialized “effector” proteins constitutes a key mechanism for transducing molecular events at chromatin to biological outcomes(1). Effector proteins influence DNA-templated processes, including transcription, DNA recombination, and DNA repair; however...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kuo, Alex J., Song, Jikui, Cheung, Peggie, Ishibe-Murakami, Satoko, Yamazoe, Sayumi, Chen, James K., Patel, Dinshaw J., Gozani, Or
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2012
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321094/ https://www.ncbi.nlm.nih.gov/pubmed/22398447 http://dx.doi.org/10.1038/nature10956

Ejemplares similares

Tissue-Specific DNA Replication Defects in Drosophila melanogaster Caused by a Meier-Gorlin Syndrome Mutation in Orc4
por: McDaniel, Stephen L., et al.
Publicado: (2020)

Meier-Gorlin syndrome
por: de Munnik, Sonja A., et al.
Publicado: (2015)

Structure and function of the Orc1 BAH-nucleosome complex
por: De Ioannes, Pablo, et al.
Publicado: (2019)

Mutations in the Pre-Replication Complex cause Meier-Gorlin syndrome
por: Bicknell, Louise S., et al.
Publicado: (2011)

Deficiency in Origin Licensing Proteins Impairs Cilia Formation: Implications for the Aetiology of Meier-Gorlin Syndrome
por: Stiff, Tom, et al.
Publicado: (2013)

Meier–Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test
por: Nazarenko, Maria S., et al.
Publicado: (2022)

A Meier-Gorlin syndrome mutation in a conserved C-terminal helix of Orc6 impedes origin recognition complex formation
por: Bleichert, Franziska, et al.
Publicado: (2013)

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome
por: McQuaid, Mary E., et al.
Publicado: (2022)

The expanding genetic and clinical landscape associated with Meier-Gorlin syndrome
por: Nielsen-Dandoroff, Emily, et al.
Publicado: (2023)

Prenatal diagnosis of Meier-Gorlin syndrome 7: a case presentation
por: Li, Xia, et al.
Publicado: (2021)

Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype
por: Yao, Likun, et al.
Publicado: (2017)

Dentofacial characteristics in a child with Meier–Gorlin syndrome: A rare case report
por: Morankar, Rahul G., et al.
Publicado: (2018)

An essential Noc3p dimerization cycle mediates ORC double-hexamer formation in replication licensing
por: Amin, Aftab, et al.
Publicado: (2023)

Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
por: Zabnenkova, Viktoriia, et al.
Publicado: (2022)

Biallelic GINS2 variant p.(Arg114Leu) causes Meier-Gorlin syndrome with craniosynostosis
por: Nabais Sá, Maria J, et al.
Publicado: (2022)

Changing protein-DNA interactions promote ORC binding site exchange during replication origin licensing
por: Zhang, Annie, et al.
Publicado: (2023)

Changing protein–DNA interactions promote ORC binding-site exchange during replication origin licensing
por: Zhang, Annie, et al.
Publicado: (2023)

Yeast ORC sumoylation status fine-tunes origin licensing
por: Regan-Mochrie, Gemma, et al.
Publicado: (2022)

The High-Affinity Interaction between ORC and DNA that Is Required for Replication Licensing Is Inhibited by 2-Arylquinolin-4-Amines
por: Gardner, Nicola J., et al.
Publicado: (2017)

Linked-read genome sequencing identifies biallelic pathogenic variants in DONSON as a novel cause of Meier-Gorlin syndrome
por: Knapp, Karen M, et al.
Publicado: (2020)

Chromosome replication: from ORC to fork
por: Nieduszynski, Conrad A, et al.
Publicado: (2001)

Regulation of replication origin licensing by ORC phosphorylation reveals a two-step mechanism for Mcm2–7 ring closing
por: Amasino, Audra, et al.
Publicado: (2023)

Regulation of replication origin licensing by ORC phosphorylation reveals a two-step mechanism for Mcm2-7 ring closing
por: Amasino, Audra L., et al.
Publicado: (2023)

The BAH domain of BAHD1 is a histone H3K27me3 reader
por: Zhao, Dan, et al.
Publicado: (2016)

Meier-Gorlin syndrome with prenatal ultrasound findings and successful growth hormone therapy: Six years follow-up of a rare case
por: Vakili, Rahim, et al.
Publicado: (2022)

Richard Meier
Publicado: (2003)

Richard Meier
por: Jodidio, Philip
Publicado: (1995)

Richard Meier
por: Cassarà, Silvio
Publicado: (1997)

A mechanism of origin licensing control through autoinhibition of S. cerevisiae ORC·DNA·Cdc6
por: Schmidt, Jan Marten, et al.
Publicado: (2022)

The structure of ORC–Cdc6 on an origin DNA reveals the mechanism of ORC activation by the replication initiator Cdc6
por: Feng, Xiang, et al.
Publicado: (2021)

Two subunits of human ORC are dispensable for DNA replication and proliferation
por: Shibata, Etsuko, et al.
Publicado: (2016)

Distinct roles of Arabidopsis ORC1 proteins in DNA replication and heterochromatic H3K27me1 deposition
por: Vergara, Zaida, et al.
Publicado: (2023)

Richard Meier, arquitecto : 1985/1991
por: Meier, Richard 1934-

Richard Meier, arquitecto : 1964/1984
por: Meier, Richard, 1934-
Publicado: (1994)

Synthesis of molecular metallic barium superhydride: pseudocubic BaH(12)
por: Chen, Wuhao, et al.
Publicado: (2021)

Coupling of H3K27me3 recognition with transcriptional repression through the BAH-PHD-CPL2 complex in Arabidopsis
por: Zhang, Yi-Zhe, et al.
Publicado: (2020)

Sid Meier's Civilization IV
Publicado: (2005)

The Replicative Consequences of Papillomavirus E2 Protein Binding to the Origin Replication Factor ORC2
por: DeSmet, Marsha, et al.
Publicado: (2016)

A conserved BAH module within mammalian BAHD1 connects H3K27me3 to Polycomb gene silencing
por: Fan, Huitao, et al.
Publicado: (2021)

Gorlin Syndrome
por: Devi, Basanti, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_5h80tvgitj6d92b5q0gt7tv12d