Detailseite
Projekt Druckansicht

Epigenetische Kontrolle des Cytomegalievirus-Chromosoms

Fachliche Zuordnung Virologie
Förderung Förderung von 2005 bis 2013
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 5450230
 
Erstellungsjahr 2014

Zusammenfassung der Projektergebnisse

Human cytomegalovirus (CMV), one of eight human herpesviruses, establishes life-long infections in most of us. CMV has long been known for causing developmental defects in human embryos and life-threatening disease in immunocompromised individuals, but preventive and therapeutic options are still very limited. The large double-stranded DNA genomes of all herpesviruses are transcribed, replicated and encapsidated in the host cell nucleus, where DNA is typically structured and maneuvred through nucleosomes. Nucleosomes individually assemble DNA around core histone octamers to form chromatin fibres. Herpesvirus DNA is devoid of histones within virion capsids. Following release into the nucleus, however, viral genomes undergo rapid nucleosome assembly by replication‐independent mechanisms, and nucleosomes occupy nuclear viral DNA in a non-random and highly predictable fashion. At early times of infection, nucleosomes associate with the CMV genome largely according to their intrinsic DNA sequence preferences, indicating that initial nucleosome formation is genetically encoded in the virus. However, as infection proceeds to the late phase, viral DNA is subject to replication-dependent nucleosome assembly, and nucleosomes redistribute extensively to establish patterns mostly determined by non-genetic factors. We propose that these factors include key regulators of viral gene expression encoded at the CMV major immediate-early (IE) locus. Indeed, mutant virus genomes deficient for IE1 expression exhibit globally increased nucleosome loads and reduced nucleosome dynamics compared with wild-type genomes. The temporal nucleosome occupancy differences between IE1-deficient and wild-type viruses correlate inversely with changes in the pattern of viral nascent and total transcript accumulation. Concurrent with the changes in nucleosome occupancy, histone modifications across the CMV genome globally change from a heterochromatin- to a euchromatin-like pattern as infection proceeds from early to late. Finally, our work defines in detail the structural basis for chromatin binding by the CMV IE1 protein. IE1 exhibits two distinct core histone binding domains, one of which (the chromatin tethering domain) targets the ‘acidic pocket’ on the nucleosome surface in a nucleic acid-independent fashion. These results provide a framework of spatial and temporal nucleosome organization and modification across the genome of a major human pathogen and suggest that a CMV major IE protein governs overall viral chromatin structure and function to regulate transcription. Exploiting chromatin targets for novel anti-viral treatment strategies may help to combat the massive health-related and economic burdens associated with CMV. Epigenie (25.07.2013): http://epigenie.com/epigenetics-goes-viral-herpes-the-histone-hijacker Science Daily (30.07.2013): http://75.101.140.165/releases/2013/07/130730163148.htm Bioscience Technology (31.07.2013): http://www.biosciencetechnology.com/news/2013/07/learning-herpes-virus Today Topics (01.08.2013): http://www.todaytopics.com/how-cells-regulate-the-human-cytomegalovirus-themechanism-by-which-genetic-information-is-packaged-and-stored/14294 Mideast Clinics Directory (01.08.2013): http://www.mideastclinics.com/healthNews/19729/GW7/How-cells-regulate-the-humancytomegalovirus%3A-the-mechanism-by-which-genetic-information-is-packaged-andstored.html#.UywCtFea81w Vaccine News Daily (01.08.2013): http://vaccinenewsdaily.com/medical_countermeasures/326395-researchers-learn-howherpes-virus-stores-information Glanzlicht Biomedizinischer Forschung (01.02.2014): http://www.ukr.de/wissenschaftler/Highlight/Februar_2014_Glanzlicht/index.php

Projektbezogene Publikationen (Auswahl)

 
 

Zusatzinformationen

Textvergrößerung und Kontrastanpassung