LEADER 05361nam 2200685Ia 450 001 9910830019203321 005 20230422044840.0 010 $a1-281-76415-9 010 $a9786611764159 010 $a3-527-61346-3 010 $a3-527-61347-1 035 $a(CKB)1000000000377229 035 $a(EBL)481967 035 $a(OCoLC)261342614 035 $a(SSID)ssj0000156888 035 $a(PQKBManifestationID)11147310 035 $a(PQKBTitleCode)TC0000156888 035 $a(PQKBWorkID)10131389 035 $a(PQKB)10460564 035 $a(MiAaPQ)EBC481967 035 $a(EXLCZ)991000000000377229 100 $a19990502d2000 uys 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aForeign DNA in mammalian systems$b[electronic resource] /$fWalter Doerfler 210 $aWeinheim ;$aNew York $cWiley-VCH$dc2000 215 $a1 online resource (197 p.) 300 $aDescription based upon print version of record. 311 $a3-527-30089-9 320 $aIncludes bibliograhical references and index. 327 $aForeign DNA in Mammalian Systems; Preface; Contents; 1 Introduction; 1.1 Further reading; 2 ForeignDNA; 2.1 Foreign DNA in the environment; 2.2 Uptake and modes of persistence of foreign DNA in mammalian cells; 2.3 Further reading; 3 Methods to detect integrated foreign DNA; 3.1 Parameters of foreign DNA integration; 3.2 The fluorescent in situ hybridization method; 3.3 Detection of foreign DNA by Southern DNA ti DNA hybridization; 3.4 Detection of foreign DNA sequences by the pol reaction (PCR); 3.5 Recloning of junction fragments and the detern nucleotide sequences 327 $a3.6 Equilibirum sedimentation in alkaline CsCl gral DNA hybridization3.7 Further reading; 4 The adenovirus paradigm; 4.1 An introduction to the adenovirus system; 4.1.1 Clinical background; 4.1.2 Virion structure; 4.1.3 Classification; 4.1.4 Multiplication during productive infection; 4.1.5 Abortive infection; 4.2 An example: Ad12 DNA integration in the Ad12 hamster cell line T637; 4.3 The state of the viral DNA in different cell systems; 4.3.1 Productive infection; 4.3.2 Abortive infection; 4.3.3 Transformation of cells in culture; 4.3.4 Tumor induction by Ad12 in newborn hamsters 327 $a4.3.5 Tumor cells in culture4.3.6 Loss of previously integrated Ad12 DNA sequences; 4.4 Adenovirus infection, DNA transfection or DNA microinjection; 4.5 Integration of adenovirus DNA in human cells - significance human somatic gene therapy; 4.6 Studies on integrative recombination of adenovirus DNA in a cell-free system; 4.7 Further reading; 5 Conclusions derived from a survey of junction sites; 5.1 On the characteristics of junction sequences; 5.2 Persistence of integrated foreign DNA - a novel functional type of insertional mutagenesis 327 $a5.3 Adenovirus DNA: chromosomal association - covalent genc integration5.4 Further reading; 6 Adenovirus-induced tumor cells and revertants; 6.1 Clonal origin of Ad12-induced tumors; 6.2 Stability - instability; 6.2.1 Hit-and-run mechanism of viral oncogenesis?; 6.2.2 General implications of a hit-and-run mechanism; 6.3 Further reading; 7 Comparisons with other viral systems; 7.1 Integration of viral DNA; 7.2 Transcription of integrated viral genomes; Color plates; 7.3 Virus-induced tumors; 7.4 Replication and integration of the retroviral genome; 7.5 Endogenous retroviral genomes 327 $a7.6 The viral archetype: integration of bacteriophage ? DNA7.6.1 The most important regulatory functions in the phage ? genome; 7.6.2 Control of transcription at the right operator OR of phage ? DNA; 7.6.3 A closer look at the integration and excision of the bacteriophage ? genome; 7.7 Further reading; 8 Non-viral systems; 8.1 Exchange of genetic information with extracellular DNA in pneumococci; 8.2 IS elements and transposons; 8.3 Thoughts on the mechanism of foreign DNA integration; 8.4 Expression of integrated foreign DNA; 8.5 Fixation of foreign DNA in transgenic animals 327 $a8.6 Critical evaluation of the results obtained with transgenic animals 330 $aIt is unlikely that the established genomes of present day organisms remain stable forever. It is conceivable that foreign DNA can gain entry into individual cells of an organism. Foreign DNA is defined as genetic material that derives from another organism of the same or a different species. The natural environment is heavily ""contaminated"" with such foreign DNA, and mammals, like other organisms, are frequently exposed to foreign DNA in their environment, notably by ingesting their daily food supply. By necessity, the gastrointestinal tract also of all mammalian organisms is constantly 606 $aGenetic transformation 606 $aMammals$xGenetics 606 $aAdenoviruses 606 $aDNA 606 $aDNA$xMethylation 615 0$aGenetic transformation. 615 0$aMammals$xGenetics. 615 0$aAdenoviruses. 615 0$aDNA. 615 0$aDNA$xMethylation. 676 $a572.819 676 $a572.8619 700 $aDoerfler$b Walter$f1933-$01653781 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830019203321 996 $aForeign DNA in mammalian systems$94005248 997 $aUNINA