In vitro Transcription of Prospect Hill virus S Genome Segment Produced by RT-PCR.
- Author:
Pyung Woo LEE
;
Man Seong PARK
- Publication Type:In Vitro ; Original Article
- MeSH:
Autoradiography;
Bacteriophage T7;
Bacteriophages;
Clone Cells;
Cloning, Organism;
DNA, Complementary;
Formaldehyde;
Gels;
Genome*;
Hantaan virus;
Hantavirus;
Nucleocapsid Proteins;
Nucleotides;
Polymerase Chain Reaction;
RNA;
Running;
Sepharose;
Uridine Triphosphate;
Viruses*
- From:Journal of the Korean Society for Microbiology
1998;33(1):39-48
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Prospect Hill virus (PHV) is related antigenically but distinct to Hantaan virus. As a member of genus Hantavirus, PHV has three segmented RNA genome. Among these segments, Small segment(S) encodes nucleocapsid protein (NP) as structural protein and also may do functional nonstructural protein(NSs). We performed in vitro transcription to produce vRNA of PHV S genome. For the first step of in vitro transcription of S genome of PHV, the S RNA segrnent which is 1,675 nucleotides long was amplified by RT-PCR using PCR primers built according to cDNA sequence of PHV S genome. Next, a new PCR primer appended above downstream primer to T7 phage promoter sequence was reconstructed to obtain PCR product containing T7 promoter. Then another PCR was performed. Using this PCR product as the template, in vitro run-off transcription without cloning by transcriptional vector was performed to obtain viral- sense RNA transcript. Thereafter, the size of transcript was assessed by running on formaldehyde agarose gels. Since the transcription reactants contain a-S UTP, the transcript is detectable by autoradiography. The transcript was also detectable by northern hybridization with a-P dCTP- labelled PHV amplicon probe (319 bp) and the initiation start point of run-off transcription was also determined by primer extention analysis. Our data indicate that the in vitro transcript could be produced from the PCR product amplified by PCR primer containing T7 phage promoter without cloning into a phage transcription vector.
