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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

GATA zinc finger domain containing 2B

p66beta, hp66beta, GATAD2B, p66/p68
Top mentioned proteins: MBD3, Histone, demethylase, p66alpha, V1a
Papers on p66beta
Towards elucidating the stability, dynamics and architecture of the nucleosome remodeling and deacetylase complex by using quantitative interaction proteomics.
Review
New
Vermeulen et al., Nijmegen, Netherlands. In Febs J, May 2015
STRUCTURED DIGITAL ABSTRACT: MBD3 physically interacts with ZNF512B, HDAC1, ZMYND8, GATAD2B, SALL4, GATAD2A, ZNF592, MTA3, ZNF687, CDK2AP1, CHD3, ZNF532, HDAC2, MTA2, CHD4, MTA1, KPNA2, CHD5, RBBP4 and RBBP7 by pull down (View interaction) CDK2AP1 physically interacts with MBD3, MTA3, HDAC2, GATAD2A, CHD4, CDK2AP1, MTA2, HDAC1, MTA1, CHD3, GATAD2B, MBD2, RBBP4 and RBBP7 by pull down (View interaction) MBD3 physically interacts with MTA2, MTA3, RBBP4, RBBP7, HDAC2, HDAC1, CHD4, CHD3 and MTA1 by cross-linking study (View interaction).
Hsa-miR-520d converts fibroblasts into CD105+ populations.
Miura et al., Tottori, Japan. In Drugs R D, 2014
Combinatorial transfection of small interfering RNAs for miR-520d-5p target genes (ELAVL2, GATAD2B, and TEAD1) produced similar results to miR-520d-5p transfection.
De novo mutations in moderate or severe intellectual disability.
Michaud et al., Montréal, Canada. In Plos Genet, 2014
A total of 12 likely pathogenic DNMs were identified in genes previously associated with ID (ARID1B, CHD2, FOXG1, GABRB3, GATAD2B, GRIN2B, MBD5, MED13L, SETBP1, TBR1, TCF4, WDR45), resulting in a diagnostic yield of ∼29%.
Identification of a nuclear protein, LRRC42, involved in lung carcinogenesis.
Nakamura et al., Tokyo, Japan. In Int J Oncol, 2014
LRRC42, which was found to localize in the nucleus of mammalian cells, is likely to interact with and stabilize GATAD2B (GATA zinc finger domain-containing 2B) and MBD3 (Methyl-CpG-binding domain protein 3) proteins that could contribute to lung cancer cell proliferation partly through the regulation of p21Waf1/Cip1.
GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila.
Kleefstra et al., Nijmegen, Netherlands. In J Med Genet, 2013
BACKGROUND: GATA zinc finger domain containing 2B (GATAD2B) encodes a subunit of the MeCP1-Mi-2/nucleosome remodelling and deacetylase complex involved in chromatin modification and regulation of transcription.
Genetic alterations in oral squamous cell carcinoma progression detected by combining array-based comparative genomic hybridization and multiplex ligation-dependent probe amplification.
Cha et al., Pusan, South Korea. In Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 2011
RESULTS: The highest amplification frequencies (100%, 7/7) were detected in FAM5B, TIPARP, PIK3CA, NLGN1, FGF10, HDAC9, GRM3, DDEF1, EDNRB, CHRDL1, and HTR2C, and the highest deletion frequencies in THRAP3, CTTNBP2NL, GATAD2B, REL, CKAP2L, RHOA, EIF4E3, PDLIM5, FBXO3, NEUROD4, and ABCA5 in the OSCC.
Foxp1/2/4-NuRD interactions regulate gene expression and epithelial injury response in the lung via regulation of interleukin-6.
Morrisey et al., Philadelphia, United States. In J Biol Chem, 2010
To determine the underlying mechanism of Foxp1/2/4-mediated transcriptional repression, a yeast two-hybrid screen was performed that identified p66beta, a transcriptional repressor and component of the NuRD chromatin-remodeling complex.
Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women.
Econs et al., Indianapolis, United States. In J Bone Miner Res, 2008
The most significant evidence of association for lumbar spine (p = 1.3 x 10(-6)) was found with rs1127091 in the GATAD2B gene.
Mutants in the mouse NuRD/Mi2 component P66alpha are embryonic lethal.
Nusse et al., Stanford, United States. In Plos One, 2006
There are two mouse and human p66 paralogs, p66alpha and p66beta.
SUMO modification enhances p66-mediated transcriptional repression of the Mi-2/NuRD complex.
Renkawitz et al., Gießen, Germany. In Mol Cell Biol, 2006
Human p66alpha and p66beta are two potent transcriptional repressors that interact with the methyl-CpG-binding domain proteins MBD2 and MBD3.
p66alpha and p66beta of the Mi-2/NuRD complex mediate MBD2 and histone interaction.
Renkawitz et al., Gießen, Germany. In Nucleic Acids Res, 2005
The function of p66alpha and of p66beta within the multiple subunits has not been addressed.
Two highly related p66 proteins comprise a new family of potent transcriptional repressors interacting with MBD2 and MBD3.
GeneRIF
Renkawitz et al., Gießen, Germany. In J Biol Chem, 2002
identification as potent transcriptional repressors interacting with MBD2 and MBD3
Identification and functional characterization of the p66/p68 components of the MeCP1 complex.
Zhang et al., Chapel Hill, United States. In Mol Cell Biol, 2002
Methylation of cytosine at CpG dinucleotides is a common feature of many higher eukaryotic genomes.
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