نتایج جستجو برای: exonucleases

تعداد نتایج: 480  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1989
S H Lee A D Kwong Y Ishimi J Hurwitz

A 120-kDa protein that blocks DNA termini has been purified from extracts of HeLa cells. This protein inhibits the action of a number of enzymes that catalyze reactions involving the 5' and 3' ends of DNA (DNA ligase, 3' and 5' exonucleases, and DNA polymerase alpha). The 120-kDa protein blocks the synthesis of long DNA chains that are normally formed during simian virus 40 DNA replication, cau...

Journal: :Nature Communications 2021

Abstract The polyadenosine tail (poly[A]-tail) is a universal modification of eukaryotic messenger RNAs (mRNAs) and non-coding (ncRNAs). In budding yeast, Pap1-synthesized mRNA poly(A) tails enhance export translation, whereas Trf4/5-mediated polyadenylation ncRNAs facilitates degradation by the exosome. Using direct RNA sequencing, we decipher extent dynamics in yeast defective all relevant ex...

2009
Marlene Oeffinger Daniel Zenklusen Angelica Ferguson Karen E. Wei Aziz El Hage David Tollervey Brian T. Chait Robert H. Singer Michael P. Rout

Ribosomal processing requires a series of endo- and exonucleolytic steps for the production of mature ribosomes, of which most have been described. To ensure ribosome synthesis, 3' end formation of rRNA uses multiple nucleases acting in parallel; however, a similar parallel mechanism had not been described for 5' end maturation. Here, we identify Rrp17p as a previously unidentified 5'-3' exonuc...

Journal: :Biochemical and biophysical research communications 2014
Emil Dedic Paulina Seweryn Anette Thyssen Jonstrup Rasmus Koch Flygaard Natalya U Fedosova Søren Vrønning Hoffmann Thomas Boesen Ditlev Egeskov Brodersen

The RNase D-type 3'-5' exonuclease Rrp6p from Saccharomyces cerevisiae is a nuclear-specific cofactor of the RNA exosome and associates in vivo with Rrp47p (Lrp1p). Here, we show using biochemistry and small-angle X-ray scattering (SAXS) that Rrp6p and Rrp47p associate into a stable, heterodimeric complex with an elongated shape consistent with binding of Rrp47p to the nuclease domain and oppos...

Journal: :Nucleic Acids Research 2006
Patricia Pérez-Arnaiz José M. Lázaro Margarita Salas Miguel de Vega

Phi29 DNA polymerase achieves a functional coupling between its 3'-5' exonuclease and polymerization activities by means of important contacts with the DNA at both active sites. The placement and orientation of residues Lys538, Lys555, Lys557, Gln560, Thr571, Thr573 and Lys575 in a modelled phi29 DNA polymerase-DNA complex suggest a DNA-binding role. In addition, crystal structure of phi29 DNA ...

Journal: :Journal of molecular biology 2006
Bethany E Dutra Susan T Lovett

A natural mutational hotspot in the thyA gene of Escherichia coli accounts for over half of the mutations that inactivate this gene, which can be selected by resistance to the antibiotic trimethoprim. This T to A transversion, at base 131 of the coding sequence, occurs within a 17 bp quasi-palindromic sequence. To clarify the mechanism of mutagenesis, we examine here cis and trans-acting factor...

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