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DNA characteristics

Nass S, Nass M (1963) Intramitochondrial fibers with DNA characteristics. J Cell Biol 19 613-628 Portier P (1918) Les symbiotes. Masson, Paris... [Pg.81]

In abiotic conditions it has been possible to obtain all four RNA bases (adenine, cytosine, guanine and uracil), but not the DNA characteristic base (thymine). In vivo, furthermore, thymine is synthesised from uracil-based precursors. [Pg.139]

At this point a brief review of certain DNA characteristics may be helpful to an understanding of the mechanisms of action of the 4-quinolones. Although the base pairing in DNA from all natural sources studied is constant, several different conformational variations of the double helix have been identified. These result from the rotational freedom inherent in the single bonds present in the ribose and phosphate backbone. The three conformational forms are called A, B, and Z. The geometry of these forms differs in the... [Pg.269]

The second critical step in homologous recombination is the isomerization and resolution of the two DNA molecules. The physical location where all four heteroduplex DNA strands meet, each base-paired with the complementary strand, is called a Holliday junction (named after Robin Holliday, who first proposed it). Figure 23.7 schematically illustrates how these DNA gymnastics are thought to occur, resulting in the formation of DNA characteristic of a homologous recombination event. Starting with the structure at the junction,... [Pg.646]

Munscher C, RiegerT, Muller-HockerJ, Kadenbach, B. (1993) The point mutation of mitochondrial DNA characteristic for MBRRF disease is found also in healthy people of different ages. PEBS Lett 317, 27-30. [Pg.86]

The DNA composition of strains is strictly specific. It is not influenced by culture conditions. It can, however, undergo punctual mutations over generations. At the laboratory culture scale, these mutations do not significantly affect the genomic DNA characteristics. Strain identification by genomic analysis therefore appears to be the most reliable approach. Several types of analysis exist which permit different levels of identification strain, species, genus. [Pg.126]

A solution leading to a successful algorithm was recently found for the folding of ribonucleic acid (RNA) [36], Natural RNA polymers (figure C2.14.1) are mainly made up from four different bases . A, C, G and U. As with DNA, multiple hydrogen bonding favours the fonnation of G-C and A-U pairs [16, 37, 38] which leads to the appearance of certain characteristic stmctures. Loop closure is considered to be the most important folding event. [Pg.2821]

Genes are DNA and carry the inheritable characteristics of an organism and these characteristics are normally expressed at the molecular level via protein synthesis Gene expression consists of two stages transcription and translation, both of which involve RNAs Sections 28 11 and 28 12 describe these RNAs and their roles m transcription and translation... [Pg.1172]

Mineralocorticoids foUow a mechanistic route similar to that of glucocorticoids, though differing in the proteins expressed. The activated MR-DNA complex promotes the expression of aldosterone-induced proteins (AIPs), which then act to increase conductance of the luminal membrane and concurrently increase pump activity of the basolateral membrane. These actions result from a number of AlP-influenced cellular characteristics,... [Pg.98]

Intoxication by aflatoxkis is referred to as aflatoxicosis. Edema and necrosis of hepatic and renal tissues seem characteristic of aflatoxicosis, and hemorrhagic enteritis accompanied by nervous symptoms often appear ki experimental animals. The mode of action of aflatoxkis kivolve an kiteraction with DNA and inhibition of the polymerases responsible for DNA and RNA synthesis (96). [Pg.480]

Ultimately a plasmid is defined by its mode of DNA repHcation. DNA repHcation is initiated at a single, characteristic sequence, termed the origin. The origin sequence determines the copy number of the plasmid relative to the host chromosome and the host enzymes that are involved in plasmid repHcation. Two different plasmids that contain the same origin sequence are termed incompatible. This term does not refer to the active exclusion of one plasmid by another from the ceU but rather to a stochastic process by which the two plasmids are partitioned differentially into progeny ceUs. A ceU which contains two plasmids of the same incompatibiHty group segregates two clonal populations, each of which has one of the two plasmids in it. [Pg.229]

The amino acid sequences of hCS-A, hCS-B, and hCS-V are shown in relation to GH in Figure 1. The sequence of hCS-V is predicted from the DNA coding sequence and apparentiy does not possess amino acids 8—55 relative to GH and the other hCS molecules. It is not certain whether hCS-V is expressed or what function it may have. Human CS-A and hCS-B share approximately 85% identity with GH and also possess the disulfide bonds between Cys 53—165 and Cys 182—189 which produce the long and short S—loops characteristic of the PRL/GH family. [Pg.181]

Recombinant DNA technology has already provided several products of therapeutic interest from mammalian cells. Table 2 gives examples of products from mammalian cells, the use, and the technology used for production. Technology development for these products has centered around the differences in characteristics of mammalian versus microbial cells, notably, the shear sensitivity and susceptibiUty to contamination of the mammalian lines. [Pg.228]

Homeoboxes code for homeodomains, sequences of 60 amino acids that function as the DNA-binding regions of transcription factors. Each homeo-box gene in Drosophila is expressed only in its own characteristic subset of embryonic cells, and almost every embryonic cell contains a unique combination of homeodomain proteins. [Pg.160]

The unique characteristic of each protein is the distinctive sequence of amino acid residues in its polypeptide chain(s). Indeed, it is the amino acid sequence of proteins that is encoded by the nucleotide sequence of DNA. This amino acid sequence, then, is a form of genetic information. By convention, the amino acid sequence is read from the N-terminal end of the polypeptide chain through to the C-terminal end. As an example, every molecule of ribonucle-... [Pg.113]


See other pages where DNA characteristics is mentioned: [Pg.248]    [Pg.428]    [Pg.1125]    [Pg.544]    [Pg.55]    [Pg.5]    [Pg.112]    [Pg.123]    [Pg.333]    [Pg.294]    [Pg.248]    [Pg.428]    [Pg.1125]    [Pg.544]    [Pg.55]    [Pg.5]    [Pg.112]    [Pg.123]    [Pg.333]    [Pg.294]    [Pg.2817]    [Pg.234]    [Pg.328]    [Pg.307]    [Pg.240]    [Pg.91]    [Pg.314]    [Pg.249]    [Pg.249]    [Pg.260]    [Pg.263]    [Pg.272]    [Pg.181]    [Pg.308]    [Pg.501]    [Pg.441]    [Pg.55]    [Pg.138]    [Pg.188]    [Pg.348]    [Pg.122]    [Pg.122]   
See also in sourсe #XX -- [ Pg.271 , Pg.272 , Pg.273 ]

See also in sourсe #XX -- [ Pg.144 ]




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Structure-Function Characteristics of Aromatic Amine-DNA Adducts

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