نتایج جستجو برای: mismatch repair system

تعداد نتایج: 2365354  

Journal: :The journals of gerontology. Series A, Biological sciences and medical sciences 2005
Simona Neri Alessandro Gardini Andrea Facchini Fabiola Olivieri Claudio Franceschi Giovanni Ravaglia Erminia Mariani

Age-related alterations of DNA repair could be involved in the accumulation of genetic damage with age. Few data suggest a possible alteration with age of the mismatch repair system, evidenced by the acquisition of microsatellite instability. We aimed to point out a possible implication of this repair system in the accumulation of genetic damage with age. Peripheral blood cell DNA from 226 part...

2012
Gagan B. Panigrahi Meghan M. Slean Jodie P. Simard Christopher E. Pearson

Background: Slipped-DNAs are mutagenic intermediates in disease-causing trinucleotide repeat instability; their processing is not well understood. Results: MutLα is required to repair single short slip-outs, and enhances repair of clustered slipouts. Conclusion: Aberrant mismatch repair attempts on clustered slip-outs may cause repeat instability. Significance: This work has determined one of t...

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: :Genetics 1989
R M Schaaper

We have previously reported that the Escherichia coli mutator strain mutD5 was defective in the correction of bacteriophage M13mp2 heteroduplex DNA containing a T.G mismatch. Here, this defect was further investigated with regard to its interaction with the mutHLS pathway of mismatch repair. A set of 15 different M13mp2 heteroduplexes was used to measure the mismatch-repair capability of wild-t...

Journal: :Cancer research 2005
Marcia R Campbell Patrick N Nation Susan E Andrew

Inheritance of a germline mutation in one of the DNA mismatch repair genes predisposes human individuals to hereditary nonpolyposis colorectal cancer, characterized by development of tumors predominantly in the colon, endometrium, and gastrointestinal tract. Mice heterozygous for a mismatch repair-null mutation generally do not have an increased risk of neoplasia. However, mice constitutively l...

Journal: :Genetics 1987
M Carraway P Youderian M G Marinus

The mismatch repair system of Escherichia coli K12 removes mispaired bases from DNA. Mismatch repair can occur on either strand of DNA if it lacks N6-methyladenines within 5'-GATC-3' sequences. In hemimethylated heteroduplexes, repair occurs preferentially on the unmethylated strand. If both strands are fully methylated, repair is inhibited. Mutant (dam-) strains of E. coli defective in the ade...

Journal: :Molecular and cellular biology 1997
H T Tran J D Keen M Kricker M A Resnick D A Gordenin

Homonucleotide runs in coding sequences are hot spots for frameshift mutations and potential sources of genetic changes leading to cancer in humans having a mismatch repair defect. We examined frameshift mutations in homonucleotide runs of deoxyadenosines ranging from 4 to 14 bases at the same position in the LYS2 gene of the yeast Saccharomyces cerevisiae. In the msh2 mismatch repair mutant, r...

2009
Anna Pluciennik Vickers Burdett Olga Lukianova Mike O'Donnell Paul Modrich

We have examined function of the bacterial beta replication clamp in the different steps of methyl-directed DNA mismatch repair. The mismatch-, MutS-, and MutL-dependent activation of MutH is unaffected by the presence or orientation of loaded beta clamp on either 3' or 5' heteroduplexes. Similarly, beta is not required for 3' or 5' mismatch-provoked excision when scored in the presence of gamm...

Journal: :Cancer Research 2004

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