نتایج جستجو برای: exonucleases

تعداد نتایج: 480  

Journal: :Advances in experimental medicine and biology 2010
Aleksander Chlebowski Rafał Tomecki María Eugenia Gas López Bertrand Séraphin Andrzej Dziembowski

The eukaryotic exosome complex is built around the backbone of a 9-subunit ring similar to phosporolytic ribonucleases such as RNase PH and polynucleotide phosphorylase (PNPase). Unlike those enzymes, the ring is devoid of any detectable catalytic activities, with the possible exception of the plant version of the complex. Instead, the essential RNA decay capability is supplied by associated hy...

Journal: :The EMBO journal 1999
M Höss P Robins T J Naven D J Pappin J Sgouros T Lindahl

Mammalian DNA polymerases alpha and beta lack 3' exonuclease activity and are unable to edit errors after DNA synthesis. However, editing exonucleases can be functions of separate polypeptides. We isolated a widely distributed DNA-specific 3' exonuclease from rabbit liver nuclei, sequenced tryptic peptides by mass spectrometry, and identified the corresponding human open reading frame. The prot...

Journal: :Microbiology 1996
R Zilhão J Plumbridge E Hajnsdorf P Régnier C M Arraiano

The rnb gene encodes ribonuclease II (RNase II), one of the two major Escherichia coli exonucleases involved in mRNA degradation. In this paper, the rnb transcript is characterized regarding its promoter and terminator regions. The combined results from S1 nuclease protection analysis, DNase I footprinting and gene fusions with lacZ have shown that rnb is expressed from two promoters. S1 nuclea...

2007
ARTWR KORNBERG

The small fragment (mol wt 36,000) produced by the limited proteolytic cleavage of DNA polymerase (mol w t 109,000) retains only the 5’ + 3’ exonuclease activity. The small fragment resembles the 5’ -+ 3’ exonuclease of the intact enzyme in degrading DNA to monoand oligonucleotides and in its capacity to excise mismatched regions such as thymine dimers. It differs from the intact enzyme in that...

Journal: :Nucleic acids research 1994
S K Shukla D McCarthy

An activity gel assay was developed for the detection of DNA helicases in crude extracts. The assay was based on the ability of DNA helicases to unwind radioactive fragments from single-stranded M13 circles that were immobilized in an SDS polyacrylamide gel. The displaced radioactive strands were detected by blotting them to a filter and visualizing the resulting bands by autoradiography. Exper...

Journal: :Molecular cell 2001
M S Junop G Obmolova K Rausch P Hsieh W Yang

The MutS protein initiates DNA mismatch repair by recognizing mispaired and unpaired bases embedded in duplex DNA and activating endo- and exonucleases to remove the mismatch. Members of the MutS family also possess a conserved ATPase activity that belongs to the ATP binding cassette (ABC) superfamily. Here we report the crystal structure of a ternary complex of MutS-DNA-ADP and assays of initi...

Journal: :EMBO reports 2006
Georg Stoecklin Thomas Mayo Paul Anderson

As an important mode of suppressing gene expression, messenger RNAs containing an AU-rich element (ARE) in the 3' untranslated region are rapidly degraded in the cytoplasm. ARE-mediated mRNA decay (AMD) is initiated by deadenylation, and in vitro studies have indicated that subsequent degradation occurs in the 3'-5' direction through a complex of exonucleases termed the exosome. An alternative ...

2013
Kazunori Watanabe Ryu Miyagawa Chie Tomikawa Rie Mizuno Akihisa Takahashi Hiroyuki Hori Kenichi Ijiri

Stress response mechanisms that modulate the dynamics of tRNA degradation and accumulation from the cytoplasm to the nucleus have been studied in yeast, the rat hepatoma and human cells. In the current study, we investigated tRNA degradation and accumulation in HeLa cells under various forms of stress. We found that initiator tRNA(Met) (tRNA(iMet)) was specifically degraded under heat stress. T...

2017
Claudia Huber Andreas Marx

Fidelity and selectivity of DNA polymerases are critical determinants for the biology of life, as well as important tools for biotechnological applications. DNA polymerases catalyze the formation of DNA strands by adding deoxynucleotides to a primer, which is complementarily bound to a template. To ensure the integrity of the genome, DNA polymerases select the correct nucleotide and further ext...

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