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

UTP20, small subunit

DRIM, Utp20, Down-regulated in Metastasis
UTP20 is a component of the U3 small nucleolar RNA (snoRNA) (SNORD3A; MIM 180710) protein complex (U3 snoRNP) and is involved in 18S rRNA processing (Wang et al., 2007 [PubMed 17498821]).[supplied by OMIM, Jun 2009] (from NCBI)
Top mentioned proteins: POLYMERASE, HAD, CAN, SET, CHIP
Papers on DRIM
Rapid dry-reagent immunomagnetic biosensing platform based on volumetric detection of nanoparticles on 3D structures.
New
Nikitin et al., Moscow, Russia. In Biosens Bioelectron, Jan 2016
UNASSIGNED: A dry-reagent immunomagnetic (DRIM) biosensing platform is developed for rapid high-precision quantitative analyses for in vitro diagnostics.
Mcm10 deficiency causes defective-replisome-induced mutagenesis and a dependency on error-free postreplicative repair.
Bielinsky et al., Minneapolis, United States. In Cell Cycle, 2013
Here, we provide evidence that the mcm10-1 allele confers alterations in DNA synthesis that lead to defective-replisome-induced mutagenesis (DRIM).
Elucidation of the assembly events required for the recruitment of Utp20, Imp4 and Bms1 onto nascent pre-ribosomes.
Dosil et al., Salamanca, Spain. In Nucleic Acids Res, 2011
In this study, we have investigated the assembly of three proteins (Utp20, Imp4 and Bms1) previously regarded as potential nucleating factors of the 90S particle.
Divergent RNA binding specificity of yeast Puf2p.
Arava et al., Haifa, Israel. In Rna, 2011
We applied an RNA-adapted version of the DRIM algorithm to identify putative binding sequences for both proteins.
Participation of DNA polymerase zeta in replication of undamaged DNA in Saccharomyces cerevisiae.
Shcherbakova et al., Omaha, United States. In Genetics, 2010
Here we present evidence that this defective-replisome-induced mutagenesis (DRIM) results from the participation of Polzeta in the copying of undamaged DNA rather than from mutagenic lesion bypass.
1A6/DRIM, a novel t-UTP, activates RNA polymerase I transcription and promotes cell proliferation.
GeneRIF
Ke et al., Beijing, China. In Plos One, 2009
1A6/DRIM activates Pol I transcription most likely by associating with both hALP and UBF and thereby affecting the acetylation of UBF
Roles of the HEAT repeat proteins Utp10 and Utp20 in 40S ribosome maturation.
GeneRIF
Tollervey et al., Edinburgh, United Kingdom. In Rna, 2007
Required for pre-ribosomal RNA processing on the pathway of 18S synthesis.
Human 1A6/DRIM, the homolog of yeast Utp20, functions in the 18S rRNA processing.
GeneRIF
Ke et al., Beijing, China. In Biochim Biophys Acta, 2007
DRIM is involved in 18S rRNA processing
Discovering motifs in ranked lists of DNA sequences.
Yakhini et al., Haifa, Israel. In Plos Comput Biol, 2007
We demonstrate the implementation of this framework in a software application, termed DRIM (discovery of rank imbalanced motifs), which identifies sequence motifs in lists of ranked DNA sequences.
Circumventing the cut-off for enrichment analysis.
Rubin, In Brief Bioinform, 2006
Three tools for threshold-free enrichment analysis of microarray data are introduced: GSEA (gene set enrichment analysis), ermineJ and DRIM (discovering rank imbalanced motifs).
Mapping nucleolar localization sequences of 1A6/DRIM.
GeneRIF
Ke et al., Beijing, China. In Febs Lett, 2006
a single region located between amino acids 2744 and 2761 at the C-terminus is capable of nucleolar accumulation. Two basic amino acid clusters within this region are essential for nucleolar accumulation.
KIAA0649, a 1A6/DRIM-interacting protein with the oncogenic potential.
Ke et al., Beijing, China. In Biochem Biophys Res Commun, 2005
We identified a 1A6/DRIM (down-regulated in metastasis) interacting protein, KIAA0649 during the yeast two-hybrid screen.
Characterization of the promoter of 1A6/DRIM, a novel cancer-related gene and identification of its transcriptional activator.
Ke et al., Beijing, China. In Gene, 2005
1A6/DRIM (Down-regulated in Metastasis) has been reported to express at a high level in the gastric cancer tissues and the premalignant lesions implicating the involvement of 1A6/DRIM in cell transformation.
The small-subunit processome is a ribosome assembly intermediate.
Baserga et al., New Haven, United States. In Eukaryot Cell, 2004
In addition to the ribosomal proteins and based on the same experimental approach, we found seven other proteins (Utp18, Noc4, Utp20, Utp21, Utp22, Emg1, and Krr1) to be bona fide SSU processome proteins.
[Preparation of a polyclonal antibody against N-terminal of 1A6/DRIM with MAPs method].
Ke et al., Beijing, China. In Beijing Da Xue Xue Bao, 2004
OBJECTIVE: To obtain the antibody against N-terminal of 1A6/DRIM, and thereafter get the profile of 1A6/DRIM expression in different cell lines.
The interrelationship between DRIM gene expression and cytogenetic and phenotypic characteristics in human breast tumor cell lines.
GeneRIF
Urquidi et al., San Diego, United States. In Bmc Genomics, 2003
Analysis of the relationship between DRIM gene expression and the metastatic phenotype of breast neoplasms.
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