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Putative catalytic component of the RNA exosome complex which has 3'->5' exoribonuclease activity and participates in a multitude of cellular RNA processing and degradation events. Zusätzlich bieten wir Ihnen DIS3 Proteine (4) und und viele weitere Produktgruppen zu diesem Protein an.
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Schizosaccharomyces pombe Polyclonal DIS3 Primary Antibody für IF, WB - ABIN2451952
Kinoshita, Goebl, Yanagida: The fission yeast dis3+ gene encodes a 110-kDa essential protein implicated in mitotic control. in Molecular and cellular biology 1991
Show all 2 Pubmed References
Human Polyclonal DIS3 Primary Antibody für IHC, IHC (p) - ABIN4305253
Tomecki, Drazkowska, Kucinski, Stodus, Szczesny, Gruchota, Owczarek, Kalisiak, Dziembowski: Multiple myeloma-associated hDIS3 mutations cause perturbations in cellular RNA metabolism and suggest hDIS3 PIN domain as a potential drug target. in Nucleic acids research 2014
Human Polyclonal DIS3 Primary Antibody für IF, WB - ABIN524835
Xie, Li, Vilborg, Lee, Shu, Yartseva, Šestan, Steitz: Mammalian 5'-capped microRNA precursors that generate a single microRNA. in Cell 2013
Human Polyclonal DIS3 Primary Antibody für ELISA, WB - ABIN564954
Niemelä, Oghabian, Staals, Greco, Pruijn, Frilander: Global analysis of the nuclear processing of transcripts with unspliced U12-type introns by the exosome. in Nucleic acids research 2014
The 3.8 A resolution cryo-EM structure of the core complex bound to a single-stranded RNA reveals that the RNA channel path is formed by two distinct features of the hDIS3 exoribonuclease: an open conformation and a domain organization more similar to bacterial RNase II than to yeast Rrp44.
Results from a study on gene variability markers in early-stage human embryos shows that DIS3 is a putative variability marker for the 3-day, 8-cell embryo stage, identified by mixture models as well as standard ANOVA.
Authors have identified a putative functional indel variant at chr13q22.1 that associates with decreased DIS3 expression in carriers of pancreatic cancer risk-increasing alleles, and could therefore affect nuclear RNA processing and/or decay.
Data indicate the pathological relevance of exosome component 11 protein (DIS3) mutations in plasma cell dyscrasias and suggest that DIS3 may represent a potential tumor suppressor gene in such disorders.
structure and function of DIS3
The study establishes that the ribonuclease DIS3, targeting LIN28B, sustains the maturation of let-7 miRNAs and suggests the increased translation of critical oncogenes as one of the biological outcomes of DIS3 inactivation.
seven novel somatic DIS3 single nucleotide variants (SNVs) and defined three hot spot mutations within the RNB domain.
Overexpression of DIS3 and LRCH1 associated with adenoma to carcinoma progression is linked to the colorectal cancer specific gain of 13q.
Multiple myeloma-associated hDIS3 mutations interfere with hDIS3 exonucleolytic activity.
Data show that hDIS3 and hDIS3L are active exonucleases, but only hDIS3 has retained endonucleolytic activity, and suggest that three different ribonucleases can serve as catalytic subunits for the exosome in human cells.
Dis3p is identical to Rrp44p, which comprises the exosome involved in ribosomal RNA processing. Similar to S. cerevisiae Dis3p, human Dis3p enhanced RCC1-stimulated nucleotide release from Ran, in a dose-dependent manner, and bound to GTP- or GDP-Ran.
Protein-protein interactions between human exosome components support the assembly of RNase PH-type subunits into a six-membered PNPase-like ring. There appears to be no interaction between human dis3 and other exosome subunits, however.
Putative catalytic component of the RNA exosome complex which has 3'->5' exoribonuclease activity and participates in a multitude of cellular RNA processing and degradation events. In the nucleus, the RNA exosome complex is involved in proper maturation of stable RNA species such as rRNA, snRNA and snoRNA, in the elimination of RNA processing by-products and non-coding 'pervasive' transcripts, such as antisense RNA species and promoter-upstream transcripts (PROMPTs), and of mRNAs with processing defects, thereby limiting or excluding their export to the cytoplasm. The RNA exosome may be involved in Ig class switch recombination (CSR) and/or Ig variable region somatic hypermutation (SHM) by targeting AICDA deamination activity to transcribed dsDNA substrates. In the cytoplasm, the RNA exosome complex is involved in general mRNA turnover and specifically degrades inherently unstable mRNAs containing AU-rich elements (AREs) within their 3' untranslated regions, and in RNA surveillance pathways, preventing translation of aberrant mRNAs. It seems to be involved in degradation of histone mRNA. DIS3 has both 3'-5' exonuclease and endonuclease activities (By similarity).
, exosome complex exonuclease RRP44
, exosome component 11
, mitotic control protein dis3 homolog
, protein DIS3 homolog
, ribosomal RNA-processing protein 44
, DIS3 mitotic control homolog (S. cerevisiae)
, DIS3 mitotic control homolog
, DIS3 exosome endoribonuclease and 3'-5' exoribonuclease
, DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease