• Title/Summary/Keyword: Thymine

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Myotonic Dystrophy Type 1 (DM1) with Multifocal White Matter Changes in Both Frontotemporoparietal Lobes (양측 전두엽, 측두-두정엽의 다초점성 백색질 변화를 보이는 1형 근육 긴장성 이영양증)

  • Lim, Jeong-Cheol;Cho, Gu-No;Kim, Eung-Gyu;Bae, Jong-Seok
    • Annals of Clinical Neurophysiology
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    • v.13 no.1
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    • pp.48-50
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    • 2011
  • Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystem disorder caused by the expansion of cytosine-thymine-guanine (CTG) repeats in the myotonic dystrophy protein kinase (DMPK) gene. Some literatures indicated that DM1 had incidental CNS lesions such as white matter lesions and diffuse gray matter atrophy. We report a patient with DM1 whose brain magnetic resonance image (MRI) showed multifocal hyperintense lesions and cystic lesion on both frontotemporoparietal lobes.

Studies on the Photoreactions of Coumarins and Furocoumarins (쿠마린과 푸로쿠마린의 광화학반응에 관한 연구)

  • Shim Sang Chul;Im Kyung Ran
    • Journal of the Korean Chemical Society
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    • v.20 no.3
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    • pp.236-239
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    • 1976
  • The mechanism of skin-sensitizing photoreactions of coumarins and furocoumarins are studied by spectroscopic, triplet quenching, and fluorescence techniques. The excited singlet mechanism is suggested for xanthotoxin-thymine/or DNA photoreactions from the results of triplet quenching studies utilizing ${\beta}$-carotene as a quencher.

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Conformational Study of Decamer DNA Duplex $d(ACGTATACGT)_2$ by NMR Spectroscopy

  • Lee, Joon-Hwa;Park, Jin-Young;Han, Hi-Jung;Park, Byong-Seok
    • Journal of the Korean Magnetic Resonance Society
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    • v.1 no.2
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    • pp.63-70
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    • 1997
  • The conformation of the self-complementary decamer duplex, d(ACGTATACGT)2 (TATA-duplex) has been studied by proton NMR spectroscopy. The duplex is essentially B-type, with distortions apparent at the TATA steps. These conformational distortion which may be preferable to occur in the thymine residue on the 5'-side, has been investigated by unusual NOE crosspeaks.

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Global Optimum Searching Technique of Multi-Modal Function Using DNA Coding Method (DNA 코딩을 이용한 multi-modal 함수의 최적점 탐색방법)

  • 백동화;강환일;김갑일;한승수
    • Proceedings of the Korean Institute of Intelligent Systems Conference
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    • 2001.12a
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    • pp.225-228
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    • 2001
  • DNA computing has been applied to the problem of getting an optimal solution since Adleman's experiment. DNA computing uses strings with various length and four-type bases that makes more useful for finding a global optimal solutions of the complex multi-modal problems. This paper presents DNA coding method for finding optimal solution of the multi-modal function and compares the efficiency of this method with the genetic algorithms (GA). GA searches effectively an optimal solution via the artificial evolution of individual group of binary string and DNA coding method uses a tool of calculation or Information store with DNA molecules and four-type bases denoted by the symbols of A(Ademine), C(Cytosine), G(Guanine) and T(Thymine). The same operators, selection, crossover, mutation, are applied to the both DNA coding algorithm and genetic algorithms. The results show that the DNA based algorithm performs better than GA.

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Analyzing Exon Structure with PCA and ICA of Short-Time Fourier Transform

  • Hwang Changha;Sohn Insuk
    • Proceedings of the Korean Statistical Society Conference
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    • 2004.11a
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    • pp.79-84
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    • 2004
  • We use principal component analysis (PCA) to identify exons of a gene and further analyze their internal structures. The PCA is conducted on the short-time Fourier transform (STFT) based on the 64 codon sequences and the 4 nucleotide sequences. By comparing to independent component analysis (ICA), we can differentiate between the exon and intron regions, and how they are correlated in terms of the square magnitudes of STFTs. The experiment is done on the gene F56F11.4 in the chromosome III of C. elegans. For this data, the nucleotide based PCA identifies the exon and intron regions clearly. The codon based PCA reveals a weak internal structure in some exon regions, but not the others. The result of ICA shows that the nucleotides thymine (T) and guanine (G) have almost all the information of the exon and intron regions for this data. We hypothesize the existence of complex exon structures that deserve more detailed analysis.

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Restriction Fragment Fingerprint of an Alkaliphilic Micrococcus sp. Y-1 Genome by Pulsed-field Gel Electrophoresis

  • Kim, Cheorl-Ho
    • Journal of Microbiology and Biotechnology
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    • v.5 no.1
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    • pp.1-5
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    • 1995
  • A genomic DNA of alkaliphilic bacterium, Micrococcus sp. Y-l, was analysed using the physical mapping method of pulsed-field gel electrophoresis (PFGE). Five restriction enzymes of Sspl, Hpal, Xbal, Ndel or EcoRI, which recognize the Adenine-Thymine-rich sequences of genomic DNA, were used for the generation of few (7 to 20) distinctly separate fragments, with average sizes in the range of 200~500 kb. However, the sites for Notl and SfiI, 8 base-recognizing enzymes, were highly frequent. The genome size of this strain was determined to be 4 mega base pairs (Mb) from restriction fragments separated by PFGE. This is the first case of restriction mapping in alkaliphilic bacterium.

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Synthesis and Antiviral Activity Evaluation of 5',5'-Difluoro-2'-methylapiosyl Nucleoside Phosphonic Acid Analogs

  • Hong, Joon Hee
    • Journal of Integrative Natural Science
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    • v.8 no.3
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    • pp.153-163
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    • 2015
  • Racemic synthesis of novel 5',5'-difluoro-2'-methyl-apiose nucleoside phosphonic acid analogs was achieved as potent antiviral agents. Phosphonation was performed by direct displacement of triflate intermediate with diethyl (lithiodifluoromethyl) phosphonate to give the corresponding (${\alpha},{\alpha}$-difluoroalkyl) phosphonate. Condensation successfully proceeded from a glycosyl donor with persilylated bases to yield the nucleoside phosphonate analogs. Deprotection of diethyl phosphonates provided the target nucleoside analogs. An antiviral evaluation of the synthesized compounds against various viruses such as HIV, HSV-1, HSV-2 and HCMV revealed that the pyrimidine analogs (cytosine, uracil, and thymine) have weak anti-HIV or HCMV activity.

DEGRADATION OF NUCLEIC ACIDS BY CELL-FREE EXTRACT OF MIXED RUMEN PROTOZOA OF BUFFALO RUMEN

  • Sinha, P.R.;Dutta, S.M..
    • Asian-Australasian Journal of Animal Sciences
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    • v.1 no.4
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    • pp.219-222
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    • 1988
  • Degradation of deoxyribonucleic acid(DNA) and ribonucleic acid(RNA) by cell-free extract of mixed rumen protozoa of buffalo rumen was investigated. DNA was observed to be degraded rapidly during an initial incubation period of 2 hr with simultaneous appearance of degradation products. RNA on the other hand recorded a rapid degradation during an initial incubation period of 1 hr. RNA degradation products appeared upto an incubation period of 2 hr. DNA was observed to degrade into oligo- and mononucleotides. pyrimidine nucleosides, purine nucleoside adenosine and bases xanthine, hypoxanthine and thymine. Degradation products of RNA comprised of pyrimidine nucleosides, purine nucleoside, adenosine and bases xanthine, hypoxanthine and uracil besides oligo- and mononucleotides.

DETERMINATION OF PURINE AND PYRIMIDINE BASES IN RUMEN MICRO-ORGANISMS BY REVERSED PHASE HPLC AFTER HYDROLYTIC DIGESTION UNDER PRESSURE

  • Han, Y.K.;Landis, J.
    • Asian-Australasian Journal of Animal Sciences
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    • v.4 no.2
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    • pp.161-164
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    • 1991
  • A rapid and accurate method is described for the determination of nucleo-bases in rumen micro-organisms. A procedure to satisfactorily hydrolyse the micro-organisms involving reaction with a mixture of readily volatile organic acids (acetic and formic acids) under high pressure, is proposed, and optimal conditions for an analytical procedure with reversed phase HPLC is described. The following nucleobases contents (mmol/kg DM) of rumen micro-organisms were found: Adenine (Ade), 82.62; Guanine (Gua), 61.34; Cytosine (Cyt), 84.61; Thymine (Thy), 35.74; Uracil (Ura), 68.62; Hypoxanthine (Hxn), 13.06; Xanthine (Xn), 8.35. Total purine-N content (g/kg N) of rumen micro-organisms were 99.60. The nucleic acid N content (g/kg N) of microbial isolates were: RNA-N, 109.9; DNA-N, 50.9.

항암성 또는 항 virus성 nucleoside 합성연구

  • 이희주
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1993.04a
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    • pp.114-114
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    • 1993
  • 항암성 또는 항 virus성 약물개발 목적으로 천연의 pyrimidine nucleoside의 구조유사체로 pyrimidine acyclonucleoside들을 합성하였다. Pyrimidine acyclonucleoside를 염기 uracil, thymine 및 5-fluorouracil을 원료로 하여 합성하고 구조를 NMR, IR data를 써서 확인하였다. 이들 합성 화합물들은 L$_{1210}$ 암세포를 이용하여 in vitro 항암성 작용을 검색하였다. 합성된 화합물들 중 5-fluorouraoil-acyclonucleoside들은 약간이나마 모 5FU보다 높은 항암성 작용을 보였다. 유도체들은 5-FU의 N$^1$에 glycosidic 결합이 아닌 alkyl 결합을 하고있어, 모 5FU를 그리 쉽게 유리시키리라 보아지지 않으므로 이들의 작용성은 acyclonucleoside형태일 것 같아 이들의 작용기전 연구가 필요하다고 보아진다. 한편 얻은 유도체들은 HSV-1 및 HSV-2를 이용하여 항 virus성 작용을 검색한 결과 2500$\mu\textrm{g}$/ml 농도에서 유의성 있는 억제 작용성을 보이지 않았다.

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