نتایج جستجو برای: uracil

تعداد نتایج: 5094  

Journal: :Current Biology 1999
Karl A. Haushalter P. Todd Stukenberg Marc W. Kirschner Gregory L. Verdine

BACKGROUND The cellular environment exposes DNA to a wide variety of endogenous and exogenous reactive species that can damage DNA, thereby leading to genetic mutations. DNA glycosylases protect the integrity of the genome by catalyzing the first step in the base excision-repair of lesions in DNA. RESULTS Here, we report a strategy to conduct genome-wide screening for expressed DNA glycosylas...

Journal: :Mutation research 2001
I Knaevelsrud P Ruoff H Anensen A Klungland S Bjelland N K Birkeland

Hydrolytic deamination of DNA-cytosines into uracils is a major source of spontaneously induced mutations, and at elevated temperatures the rate of cytosine deamination is increased. Uracil lesions are repaired by the base excision repair pathway, which is initiated by a specific uracil DNA glycosylase enzyme (UDG). The hyperthermophilic archaeon Archaeoglobus fulgidus contains a recently chara...

Journal: :Journal of experimental botany 2006
George S Mourad Bryan M Snook Joshua T Prabhakar Tyler A Mansfield Neil P Schultes

A fluoroorotic acid (FOA)-resistant mutant of Arabidopsis thaliana was isolated by screening M2 populations of ethyl methane sulphonate (EMS)-mutagenized Columbia seed. FOA resistance was due to a nuclear recessive gene, for1-1, which locates to a 519 kb region in chromosome 5. Assays of key regulatory enzymes in de novo pyrimidine synthesis (uridine monophosphate synthase) and salvage biochemi...

Journal: :Nucleic Acids Research 2006
Lauren Seiple Pawel Jaruga Miral Dizdaroglu James T. Stivers

5-fluorouracil (5-FU) is a widely used anticancer drug that disrupts pyrimidine nucleotide pool balances and leads to uracil incorporation in DNA, which is then recognized and removed by the uracil base excision repair (BER) pathway. Using complementary biochemical and genetic approaches we have examined the role of uracil BER in the cell killing mechanism of 5-FU. A yeast strain lacking the en...

Journal: :Cell 1995
Clifford D Mol Andrew S Arvai Russell J Sanderson Geir Slupphaug Bodil Kavli Hans E Krokan Dale W Mosbaugh John A Tainer

Uracil-DNA glycosylase inhibitor (Ugi) is a B. subtilis bacteriophage protein that protects the uracil-containing phage DNA by irreversibly inhibiting the key DNA repair enzyme uracil-DNA glycosylase (UDG). The 1.9 A crystal structure of Ugi complexed to human UDG reveals that the Ugi structure, consisting of a twisted five-stranded antiparallel beta sheet and two alpha helices, binds by insert...

Journal: :Nucleic Acids Research 2006
Daniel J. Krosky Mario A. Bianchet Lauren Seiple Suhman Chung L. Mario Amzel James T. Stivers

Human nuclear uracil DNA glycosylase (UNG2) is a cellular DNA repair enzyme that is essential for a number of diverse biological phenomena ranging from antibody diversification to B-cell lymphomas and type-1 human immunodeficiency virus infectivity. During each of these processes, UNG2 recognizes uracilated DNA and excises the uracil base by flipping it into the enzyme active site. We have take...

Journal: :Organic & biomolecular chemistry 2012
Tianfang Wang John H Bowie

This theoretical study investigates possible synthetic routes to cytosine, uracil and thymine in the gas phase from precursor molecules that have been detected in interstellar media. Studies at the CCSD(T)/6-311++G(d,p)//B3LYP/6-311++G(d,p) level of theory suggest that: The reactions between :CCCNH and :CCCO with monosolvated urea may constitute viable interstellar syntheses of cytosine and ura...

Journal: :Chemical communications 2013
Sibasish Paul Santanu Jana Jhuma Bhadra Surajit Sinha

Synthesis, photophysical properties and submicron ring formation of functionalized uracil morpholino monomers have been reported. A series of characterization techniques indicated that the rings are formed by the inter-molecular hydrogen bonding of the uracil nucleus having a trityl-protected morpholino moiety. This is the smallest nucleoside unit known to date for submicron size ring formation.

Journal: :Journal of Biological Chemistry 1958

2009
Henry J. Russell Tomas T. Richardson Kieran Emptage Bernard A. Connolly

Archaeal family B polymerases bind tightly to the deaminated bases uracil and hypoxanthine in single-stranded DNA, stalling replication on encountering these pro-mutagenic deoxynucleosides four steps ahead of the primer-template junction. When uracil is specifically bound, the polymerase-DNA complex exists in the editing rather than the polymerization conformation, despite the duplex region of ...

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