Dataset Information

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

ABSTRACT: Minute virus of mice (MVM) replicates via a linearized form of rolling-circle replication in which the viral nickase, NS1, initiates DNA synthesis by introducing a site-specific nick into either of two distinct origin sequences. In vitro nicking and replication assays with substrates that had deletions or mutations were used to explore the sequences and structural elements essential for activity of one of these origins, located in the right-end (5') viral telomere. This structure contains 248 nucleotides, most-favorably arranged as a simple hairpin with six unpaired bases. However, a pair of opposing NS1 binding sites, located near its outboard end, create a 33-bp palindrome that could potentially assume an alternate cruciform configuration and hence directly bind HMG1, the essential cofactor for this origin. The palindromic nature of this sequence, and thus its ability to fold into a cruciform, was dispensable for origin function, as was the NS1 binding site occupying the inboard arm of the palindrome. In contrast, the NS1 site in the outboard arm was essential for initiation, even though positioned 120 bp from the nick site. The specific sequence of the nick site and an additional NS1 binding site which directly orients NS1 over the initiation site were also essential and delimited the inboard border of the minimal right-end origin. DNase I and hydroxyl radical footprints defined sequences protected by NS1 and suggest that HMG1 allows the NS1 molecules positioned at each end of the origin to interact, creating a distortion characteristic of a double helical loop.

SUBMITTER: Cotmore SF

PROVIDER: S-EPMC111468 | biostudies-literature | 2000 Feb

REPOSITORIES: biostudies-literature

ACCESS DATA

Publications

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

Cotmore S F SF Christensen J J Tattersall P P

Journal of virology 20000201 3

Minute virus of mice (MVM) replicates via a linearized form of rolling-circle replication in which the viral nickase, NS1, initiates DNA synthesis by introducing a site-specific nick into either of two distinct origin sequences. In vitro nicking and replication assays with substrates that had deletions or mutations were used to explore the sequences and structural elements essential for activity of one of these origins, located in the right-end (5') viral telomere. This structure contains 248 nu ...[more]

PMID: 10627544

Similar Datasets

Project description:Passive acoustic monitoring is an important tool for studying marine mammals. Ocean bottom seismometer networks provide data sets of opportunity for studying blue whales (Balaenoptera musculus) which vocalize extensively at seismic frequencies. We describe methods to localize calls and obtain tracks using the B call of northeast Pacific blue whale recorded by a large network of widely spaced ocean bottom seismometers off the coast of the Pacific Northwest. The first harmonic of the B call at ~15 Hz is detected using spectrogram cross-correlation. The seasonality of calls, inferred from a dataset of calls identified by an analyst, is used to estimate the probability that detections are true positives as a function of the strength of the detection. Because the spacing of seismometers reaches 70 km, faint detections with a significant probability of being false positives must be considered in multi-station localizations. Calls are located by maximizing a likelihood function which considers each strong detection in turn as the earliest arrival time and seeks to fit the times of detections that follow within a feasible time and distance window. An alternative procedure seeks solutions based on the detections that maximize their sum after weighting by detection strength and proximity. Both approaches lead to many spurious solutions that can mix detections from different B calls and include false detections including misidentified A calls. Tracks that are reliable can be obtained iteratively by assigning detections to localizations that are grouped in space and time, and requiring groups of at least 20 locations. Smooth paths are fit to tracks by including constraints that minimize changes in speed and direction while fitting the locations to their uncertainties or applying the double difference relocation method. The reliability of localizations for future experiments might be improved by increasing sampling rates and detecting harmonics of the B call.

Dataset Information

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

Publications

Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets