Julias, John G., Pathak, Vinay K.
Deoxyribonucleoside triphosphate (dNTP) pool imbalances are associated with an increase in the rate of misincorporation and hypermutation during in vitro reverse transcription reactions. However, the...
Julias, John G., Ferris, Andrea L., Boyer, Paul L., Hughes, Stephen H.
The amount of excess polymerase and RNase H activity in human immunodeficiency virus type 1 virions was measured by using vectors that undergo a single round of replication. Vectors containing...
Julias, John G., McWilliams, Mary Jane, Sarafianos, Stefan G., Arnold, Edward, Hughes, Stephen H.
Retroviral reverse transcriptases contain a DNA polymerase activity that can copy an RNA or DNA template and an RNase H activity that degrades the viral RNA genome during reverse transcription. RNase...
Hodge, Deborah L., Martinez, Alfredo, Julias, John G., Taylor, Lynn S., Young, Howard A.
Posttranscriptional control of gamma interferon (IFN-γ) gene expression has not been extensively studied and is poorly understood. Our work describes a posttranscriptional mechanism that modulates...
Construction and Characterization of a Replication-Competent Retroviral Shuttle Vector Plasmid
Oh, Jangsuk, Julias, John G., Ferris, Andrea L., Hughes, Stephen H.
We constructed two versions of an RCASBP-based retroviral shuttle vector, RSVP (RCASBP shuttle vector plasmid), containing either the zeocin or blasticidin resistance gene. In this vector, the drug...
Julias, John G., McWilliams, Mary Jane, Sarafianos, Stefan G., Alvord, W. Gregory, Arnold, Edward, Hughes, Stephen H.
The crystal structure of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase in a complex with an RNA-DNA template-primer identified amino acids in the connection domain that make...
McWilliams, Mary Jane, Julias, John G., Sarafianos, Stefan G., Alvord, W. Gregory, Arnold, Edward, Hughes, Stephen H.
The RNase H activity of retroviral reverse transcriptases (RTs) degrades viral genomic RNA after it has been copied into DNA, removes the tRNA used to initiate negative-strand DNA synthesis, and...
Julias, John G., McWilliams, Mary Jane, Sarafianos, Stefan G., Alvord, W. Gregory, Arnold, Eddy, Hughes, Stephen H.
The RNase H cleavages that generate and remove the polypurine tract (PPT) primer during retroviral reverse transcription must be specific in order to create a linear viral DNA that is suitable for...
Chang, Kevin W., Julias, John G., Alvord, W. Gregory, Oh, Jangsuk, Hughes, Stephen H.
Retroviral polypurine tracts (PPTs) serve as primers for plus-strand DNA synthesis during reverse transcription. The generation and removal of the PPT primer requires specific cleavages by the RNase...
Ambrose, Zandrea, Julias, John G., Boyer, Paul L., KewalRamani, Vineet N., Hughes, Stephen H.
We investigated the relationship between the level of reverse transcriptase (RT) in human immunodeficiency virus type 1 (HIV-1) particles and susceptibility to nonnucleoside reverse transcriptase...
Julias, John G., Pathak, Vinay K.
Deoxyribonucleoside triphosphate (dNTP) pool imbalances are associated with an increase in the rate of misincorporation and hypermutation during in vitro reverse transcription reactions. However, the...
Julias, John G., Ferris, Andrea L., Boyer, Paul L., Hughes, Stephen H.
The amount of excess polymerase and RNase H activity in human immunodeficiency virus type 1 virions was measured by using vectors that undergo a single round of replication. Vectors containing...
Julias, John G., McWilliams, Mary Jane, Sarafianos, Stefan G., Arnold, Edward, Hughes, Stephen H.
Retroviral reverse transcriptases contain a DNA polymerase activity that can copy an RNA or DNA template and an RNase H activity that degrades the viral RNA genome during reverse transcription. RNase...
Hodge, Deborah L., Martinez, Alfredo, Julias, John G., Taylor, Lynn S., Young, Howard A.
Posttranscriptional control of gamma interferon (IFN-γ) gene expression has not been extensively studied and is poorly understood. Our work describes a posttranscriptional mechanism that modulates...
Construction and Characterization of a Replication-Competent Retroviral Shuttle Vector Plasmid
Oh, Jangsuk, Julias, John G., Ferris, Andrea L., Hughes, Stephen H.
We constructed two versions of an RCASBP-based retroviral shuttle vector, RSVP (RCASBP shuttle vector plasmid), containing either the zeocin or blasticidin resistance gene. In this vector, the drug...
Julias, John G., McWilliams, Mary Jane, Sarafianos, Stefan G., Alvord, W. Gregory, Arnold, Edward, Hughes, Stephen H.
The crystal structure of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase in a complex with an RNA-DNA template-primer identified amino acids in the connection domain that make...
McWilliams, Mary Jane, Julias, John G., Sarafianos, Stefan G., Alvord, W. Gregory, Arnold, Edward, Hughes, Stephen H.
The RNase H activity of retroviral reverse transcriptases (RTs) degrades viral genomic RNA after it has been copied into DNA, removes the tRNA used to initiate negative-strand DNA synthesis, and...
Julias, John G., McWilliams, Mary Jane, Sarafianos, Stefan G., Alvord, W. Gregory, Arnold, Eddy, Hughes, Stephen H.
The RNase H cleavages that generate and remove the polypurine tract (PPT) primer during retroviral reverse transcription must be specific in order to create a linear viral DNA that is suitable for...
Chang, Kevin W., Julias, John G., Alvord, W. Gregory, Oh, Jangsuk, Hughes, Stephen H.
Retroviral polypurine tracts (PPTs) serve as primers for plus-strand DNA synthesis during reverse transcription. The generation and removal of the PPT primer requires specific cleavages by the RNase...
Ambrose, Zandrea, Julias, John G., Boyer, Paul L., KewalRamani, Vineet N., Hughes, Stephen H.
We investigated the relationship between the level of reverse transcriptase (RT) in human immunodeficiency virus type 1 (HIV-1) particles and susceptibility to nonnucleoside reverse transcriptase...
Oh, Jangsuk, McWilliams, Mary Jane, Julias, John G., Hughes, Stephen H.
In retroviruses, the first nucleotide added to the tRNA primer defines the end of the U5 region in the right long terminal repeat, and the subsequent removal of this tRNA primer by RNase H exactly...