6533b7d4fe1ef96bd126247b
RESEARCH PRODUCT
Parvovirus nonstructural protein 2 interacts with chromatin-regulating cellular proteins
Salla MattolaKari SalokasVesa AhoElina MäntyläSami SalminenSatu HakanenEinari A. NiskanenJulija SvirskaiteTeemu O. IhalainenKari J. AirenneMinna Kaikkonen-määttäColin R. ParrishMarkku VarjosaloMaija Vihinen-rantasubject
11832 Microbiology and virologyparvovirusesvirusesvirus diseasesViral Nonstructural Proteinsbiochemical phenomena metabolism and nutritionVirus ReplicationinfektiotChromatinCell Linecellular proteinsParvoviridae InfectionsParvovirusHumans1182 Biochemistry cell and molecular biology3111 Biomedicineproteiinitparvoviruksetdescription
Autonomous parvoviruses encode at least two nonstructural proteins, NS1 and NS2. While NS1 is linked to important nuclear processes required for viral replication, much less is known about the role of NS2. Specifically, the function of canine parvovirus (CPV) NS2 has remained undefined. Here we have used proximity-dependent biotin identification (BioID) to screen for nuclear proteins that associate with CPV NS2. Many of these associations were seen both in noninfected and infected cells, however, the major type of interacting proteins shifted from nuclear envelope proteins to chromatin-associated proteins in infected cells. BioID interactions revealed a potential role for NS2 in DNA remodeling and damage response. Studies of mutant viral genomes with truncated forms of the NS2 protein suggested a change in host chromatin accessibility. Moreover, further studies with NS2 mutants indicated that NS2 performs functions that affect the quantity and distribution of proteins linked to DNA damage response. Notably, mutation in the splice donor site of the NS2 led to a preferred formation of small viral replication center foci instead of the large coalescent centers seen in wild-type infection. Collectively, our results provide insights into potential roles of CPV NS2 in controlling chromatin remodeling and DNA damage response during parvoviral replication. publishedVersion Peer reviewed
year | journal | country | edition | language |
---|---|---|---|---|
2022-04-08 |