Chromatin Structure of the Integrated Viral Sequences in Adenovirus-transformed Cells


Book Description

In the eukaryotic cell nucleus, chromatin is organized into higher-order structures through hierarchical levels of folding and coiling. Active genes are contained in chromatin domains with a more "open" conformation that is preferentially sensitive to DNase 1 digestion compared to inactive chromatin. The spatial organization of chromatin is maintained by the nuclear matrix, the major structural component of the nucleus. Chromosomal DNA is organized into supercoiled loops anchored at their bases to the nuclear matrix, and in most cases examined, active genes are located at or near the base of the loops. -- I have examined the DNase 1 sensitivity of the integrated viral sequences of four adenovirus type 5-transformed cell lines, and the organization of these sequences relative to the nuclear matrix. DNase 1 sensitivity was analysed by digesting nuclei with DNase 1 and monitoring the disappearance of virus-specific restriction fragments by Southern blotting and hybridization. In each cell line, the integrated viral sequences were in a conformation typical of active chromatin, i.e. they were preferentially sensitive to DNase 1 compared to inactive chromatin. The DNase 1 sensitive region included not only the active transforming (E1) genes, but extended into the adjacent inactive viral sequences. Thus, the integrated viral sequences were contained within active chromatin domains. -- In addition to these extended domains, DNase 1 hypersensitive sites were detected in the E1A 5'-flanking sequences. These sites were mapped to sequences previously shown to contain the E1A transcriptional enhancers and binding sites for cellular transcription factors. Therefore, the DNase 1 hypersensitive sites likely reflect alterations in local chromatin structure associated with regulation of transcription of the integrated E1A genes. -- The organization of the integrated viral sequences relative to the nuclear matrix was analysed by assessing the matrix associated and non-associated DNA fractions for their content of viral sequences by Southern blotting and hybridization. There was no enrichment or depletion of the viral sequences in either of these fractions relative to total unfractionated DNA, consistent with a random organization relative to the nuclear matrix. However, control studies indicated that these results may be due to the conditions used to isolate the nuclear matrix DNA fractions. - (Keywords: adenovirus type 5; chromatin domain; DNase 1 sensitivity; hypersensitive sites; nuclear matrix.).







Adenovirus DNA


Book Description

Although adenoviruses have been established for quite some time as one of the most pliable tools to study the molecular biology of mammalian cells, rapid progress continues to be made with this virus system. The adenoviral genome introduced into the nucleus of cells as a Trojan Horse, as it were, is now facili­ tating investigators to uncover details of cellular mechanisms. In this volume twelve chapters have been collected that summarize important current research on different mechanisms in adenovirus­ infected and -transformed cells. It has become increasingly apparent that some of these mechanisms do not only pertain to highly specialized strategies of the viral genome and its expres­ sion or replication, but may simultaneously shed light on events indigenous to the cell. "Adenovirus DNA: The Viral Genome and its Expression" high­ lights the first publication of the entire annotated sequence of 35. 937 nucleotide pairs of adenovirus type 2 DNA by the Cold Spring Harbor and Uppsala groups (chapter 1). Goran Akusjarvi, Ulf Pettersson (Uppsala University) and Rich Roberts (Cold Spring Harbor) present a survey on the structure and function of the adenovirus-2 genome (chapter 2). A considerable amount of in­ formation has been collected on the biochemical mechanisms in­ vol ved in adenov irus DNA repl ication in human cells. Al though highly specialized in the way of initiating DNA replication, adenov irus DNA repl ication represents probably one of the best studied systems in work on eukaryotic DNA replication.






















Foreign DNA in Mammalian Systems


Book Description

It 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 in contact with foreign DNA. So far, next to nothing is known about defense mechanisms in mammals against the intrusion of foreign DNA. At least in cells growing in culture, the uptake and genomic fixation by integration of foreign DNA can readily be demonstrated. For a number of reasons, the author has considered it important to investigate the phenomena and mechanisms involved in the interaction of foreign DNA with mammalian cells and organisms in detail.