1.Environments of ethidium binding to allosteric Dna: II. Accessibility, mobility and mode of binding.
Experimental & Molecular Medicine 2000;32(4):204-209
DNA binding compounds were previously shown to bind to the right-handed DNA forms and hybrid B-Z forms in a highly cooperative manner and indicate that structural specificity plays a key role in a ligand binding to DNA. In this study, the modes of binding and structural specificity of agents to unusual DNA are examined by a variety of fluorescence techniques (intensity, polarization and quenching, etc.) to explore a reliable method to detect the association environment of ligands to deoxyoligonucleotides initially containing a B-Z junction between the left-handed Z-DNA and right-handed B-DNA. The results of fluorescence energy transfer measurement demonstrated that the ligand molecules bind to the allosterically converted DNA structures by intercalation. In the absence of high-resolution structural data, this fluorescence energy transfer measurement allowed reliable measures and infer the binding environment of ligands to the allosteric DNA structures.
Allosteric Regulation
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Circular Dichroism
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DNA/*chemistry/*metabolism
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Energy Transfer
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Ethidium/*metabolism
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Exodeoxyribonucleases/metabolism
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Ligands
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Motion
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Nucleic Acid Conformation
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Oligodeoxyribonucleotides/*metabolism
2.Correlation between the methylation of SULF2 and WRN promoter and chemosensitivity to irinotecan in gastric cancer.
Lin WANG ; Jie SHEN ; Li-juan MENG ; Wei-fei FAN ; Jun WANG ; Bao-rui LIU
Chinese Journal of Oncology 2013;35(6):418-422
OBJECTIVETo explore the relationship between SULF2 and WRN promoter methylation and chemosensitivity to irinotecan, and also the clinicopathological features in patients with gastric cancer.
METHODSThe chemosensitivity to irinotecan was tested by MTT assay. The methylation of SULF2 and WRN promoter in the fresh gastric cancer tissues was detected by methylation specific PCR. The differences of chemosensitivity and clinicopathological features of the methylation group were compared with that of the non-methylation group. The tumor growth in nude mice bearing human gastric cancer xenografts treated with CPT-11was also observed.
RESULTSThe methylation rates of SULF2 and WRN were 28.4% (29/102) and 23.5% (24/102), respectively. There were no significant association between promoter methylation and clinicopathological features of patients including age, gender, histologic type, lymphatic invasion, and TNM Stage. In all the 102 cases, there were 30 cases of irrinotecan-sensitive group, and 72 cases of the irrinotecan-resistant group. The SULF2 methylation rate was 46.7% (14/30)in the sensitive group, and 20.8% (15/72) in the resistant group (P = 0.008),The WRN methylation rate was 33.3% (10/30) in the sensitive group, and 19.4% (14/72) in the resistant group (P = 0.214). Gastric cancer tissues were more sensitive to irrinotecan when both the genes were methylated. The nude mice bearing human gastric cancer xenografts with SULF2 methylation were more sensitive to irrinotecan.
CONCLUSIONSThe detection of SULF2 and WRN promoter methylation may provide evidence for screening and targeting the most sensitive gastric cancer subpopulation suitable for personalized irrinotecan chemotherapy.
Antineoplastic Agents, Phytogenic ; pharmacology ; Camptothecin ; analogs & derivatives ; pharmacology ; DNA Methylation ; Exodeoxyribonucleases ; metabolism ; Humans ; Methylation ; Promoter Regions, Genetic ; RecQ Helicases ; metabolism ; Stomach Neoplasms ; metabolism ; Sulfotransferases ; metabolism ; Werner Syndrome Helicase
3.Human KIAA1018/FAN1 nuclease is a new mitotic substrate of APC/C(Cdh1).
Fenju LAI ; Kaishun HU ; Yuanzhong WU ; Jianjun TANG ; Yi SANG ; Jingying CAO ; Tiebang KANG
Chinese Journal of Cancer 2012;31(9):440-448
A recently identified protein, FAN1 (FANCD2-associated nuclease 1, previously known as KIAA1018), is a novel nuclease associated with monoubiquitinated FANCD2 that is required for cellular resistance against DNA interstrand crosslinking (ICL) agents. The mechanisms of FAN1 regulation have not yet been explored. Here, we provide evidence that FAN1 is degraded during mitotic exit, suggesting that FAN1 may be a mitotic substrate of the anaphase-promoting cyclosome complex (APC/C). Indeed, Cdh1, but not Cdc20, was capable of regulating the protein level of FAN1 through the KEN box and the D-box. Moreover, the up- and down-regulation of FAN1 affected the progression to mitotic exit. Collectively, these data suggest that FAN1 may be a new mitotic substrate of APC/CCdh1 that plays a key role during mitotic exit.
Anaphase-Promoting Complex-Cyclosome
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Bone Neoplasms
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metabolism
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pathology
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Cadherins
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genetics
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metabolism
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Cdc20 Proteins
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Cell Cycle Proteins
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genetics
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metabolism
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Cell Line, Tumor
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Exodeoxyribonucleases
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genetics
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metabolism
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HEK293 Cells
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Humans
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Mitosis
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Osteosarcoma
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metabolism
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pathology
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Ubiquitin-Protein Ligase Complexes
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genetics
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metabolism
4.The Fanconi anemia pathway and DNA interstrand cross-link repair.
Protein & Cell 2011;2(9):704-711
Fanconi anemia (FA) is an autosomal or X-linked recessive disorder characterized by chromosomal instability, bone marrow failure, cancer susceptibility, and a profound sensitivity to agents that produce DNA interstrand cross-link (ICL). To date, 15 genes have been identified that, when mutated, result in FA or an FA-like syndrome. It is believed that cellular resistance to DNA interstrand cross-linking agents requires all 15 FA or FA-like proteins. Here, we review our current understanding of how these FA proteins participate in ICL repair and discuss the molecular mechanisms that regulate the FA pathway to maintain genome stability.
DNA Damage
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DNA Repair
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Exodeoxyribonucleases
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genetics
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metabolism
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Fanconi Anemia
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genetics
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metabolism
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pathology
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Fanconi Anemia Complementation Group N Protein
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Fanconi Anemia Complementation Group Proteins
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genetics
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metabolism
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Humans
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Nuclear Proteins
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genetics
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metabolism
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Recombinases
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genetics
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metabolism
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Tumor Suppressor Proteins
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genetics
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metabolism
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Ubiquitination
5.Detection of interaction of binding affinity of aromatic hydrocarbon receptor to the specific DNA by exonuclease protection mediated PCR assay.
Journal of Huazhong University of Science and Technology (Medical Sciences) 2005;25(1):104-6
A novel exonuclease protection mediated PCR assay (EPM-PCR) to detect the interaction of protein and DNA at a dioxin-responsive enhancer (DRE) upstream of the CYP1A1 gene in rat hepatic cytosol was established. A double-stranded DNA fragment containing two binding sites was designed and incubated with the aryl hydrocarbon receptor (AhR) transformed by 2,3,7,8-tetrachlorodibenzo-p dioxin (TCDD) to generate TCDD: AhR: DNA complex which could protect receptor-binding DNA against exonuclease II (Exo III) digestion. With Exo III treatment, free DNAs were digested and receptor-bound DNAs remained that could be amplified by PCR. By agarose gel electrophoreses a clear band (285bp) was detected using TCDD-treated sample, while nothing with control samples. To detect transformed AhR-DRE complex, 2 fmol DNAs and 3 ug cytosol proteins were found to be sufficient in the experiment. Compared with gel retardation assay, this new method is more sensitive for monitoring the Ah receptor-enhancer interaction without radioactive pollution.
Binding Sites
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Cytochrome P-450 CYP1A1/*genetics
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Cytosol/metabolism
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DNA-Binding Proteins/chemistry
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Exodeoxyribonucleases/chemistry
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Liver/*metabolism
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Polymerase Chain Reaction
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Rats, Sprague-Dawley
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Receptors, Aryl Hydrocarbon/*chemistry
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Tetrachlorodibenzodioxin/*analogs & derivatives
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Tetrachlorodibenzodioxin/chemistry
6.Red/ET recombination and its biomedical applications.
Jun-Ping WANG ; You-Ming ZHANG
Chinese Journal of Biotechnology 2005;21(3):502-506
Red/ET recombination, a powerful homologous recombination system based on the Red operon of lambda phage or RecE/ RecT from Rac phage, provides an innovative approach for DNA engineering. Deletion, insertion and mutation can be quickly and precisely performed on the target gene mediated by Red/ET recombination with PCR derived DNA fragments or oligonucleotides. This technical platform has extensive applications in biomedical field including bacterial artificial chromosome modification, gene knock-out construction and genetic modification of E. coli strains as well as some other kinds of microorganisms. Recently, Red/ET recombination was improved in several aspects so that it becomes more powerful and maneuverable. The characteristic and development of Red/ET recombination and its biomedical applications were described in this review.
Bacteriophage lambda
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genetics
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DNA, Recombinant
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genetics
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DNA-Binding Proteins
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genetics
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Escherichia coli
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genetics
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metabolism
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Escherichia coli Proteins
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genetics
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Exodeoxyribonucleases
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genetics
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Genetic Engineering
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methods
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Rec A Recombinases
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genetics
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Recombination, Genetic
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genetics