NDLI: Binding of the herpes simplex virus type 1 UL9 gene product to an origin of viral DNA replication.

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Fidelity of human immunodeficiency virus type I reverse transcriptase in copying natural DNA.

Sequence organization and gene expression of pGD1, a plasmid found in a wild isolate of Dictyostelium.

Binding of the herpes simplex virus type 1 UL9 gene product to an origin of viral DNA replication.

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The anonymous DNA probe p7-26 identifying the locus [D7S17], reveals an XmnI polymorphism.

RFLP identified by the anonymous DNA segment FZ IV E11 at 1p23 [HGM9 no.D1S87]

RFLP identified by the anonymous DNA segment OLVIID1 on chromosome 6 [HGM9 no.D6S47]

RFLP identified by the anonymous DNA segment OLVIIF5 at 21q22.1-22.3 [HGM9 no.D21S143]

RFLP identified by the anonymous DNA segment FZ V D11 at 22q13 [HGM9 no.D22S80]

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Probe pJ1 [D7S402] detects a MspI RFLP on chromosome 7q31-32.

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Binding of the herpes simplex virus type 1 UL9 gene product to an origin of viral DNA replication.

Content Provider	PubMed Central
Author	Weir, H. M. Calder, J. M. Stow, N. D.
Abstract	The binding of a herpes simplex virus type 1 (HSV-1) encoded polypeptide to a viral origin of DNA replication has been studied by using a gel retardation assay. Incubation of nuclear extract from HSV-1 infected cells with a labelled origin-containing fragment resulted in the formation of a specific retarded complex, the migration of which was further reduced in the presence of an antibody reactive with the UL9 gene product. Introduction of an additional copy of the UL9 gene, under the control of an immediate early (IE) promoter, conferred the ability to express origin binding activity at the non-permissive temperature upon an HSV-1 ts mutant blocked at the IE stage of infection. Endogenous or exogenous proteolytic activity revealed the presence of a relatively protease-resistant domain which retained sequence-specific DNA binding activity. The C-terminal 317 amino acids of the UL9 gene expressed as a fusion protein in Escherichia coli also bound to the origin. Our results demonstrate that the UL9 gene product binds to a viral origin and that sequence specific recognition and binding are specified by the C-terminal 37% of the polypeptide.
Starting Page	1409
File Format	PDF
ISSN	13624962
e-ISSN	13624962
Journal	Nucleic Acids Research
Issue Number	4
Volume Number	17
Language	English
Publisher Date	1989-02-25
Access Restriction	Open
Subject Keyword	Research in Higher Education
Content Type	Text
Resource Type	Article
Subject	Genetics

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