TWiV 66: Reverse transcription

January 17, 2010

Hosts: Vincent Racaniello and Dickson Despommier

Vincent and Dickson continue virology 101 with a discussion of information flow from RNA to DNA, a process known as reverse transcription, which occurs in cells infected with retroviruses, hepatitis B virus, cauliflower mosaic virus, foamy viruses, and even in uninfected cells.

This episode is sponsored by Data Robotics Inc. To receive $50 off a Drobo or $100 off a Drobo S, visit drobostore.com and use the promotion code VINCENT.

Play

Click the arrow above to play, or right-click to download TWiV #66 (50 MB .mp3, 68 minutes)

Subscribe to TWiV (free) in iTunes , at the Zune Marketplace, by the RSS feed, or by email.

Links for this episode:

Weekly Science Picks
Vincent Joint UN Programme on HIV/AIDS

Send your virology questions and comments (email or mp3 file) to twiv@twiv.tv or leave voicemail at Skype: twivpodcast. You can also post articles that you would like us to discuss at microbeworld.org and tag them with twiv.

  • Pingback: Tweets that mention TWiV 66: Reverse transcription -- Topsy.com

  • Pingback: uberVU - social comments

  • dakezhang

    can not download your great podcast from itunes…wonder if there is something wrong….
    thx…

  • http://www.virology.ws profvrr

    I don't have a problem downloading this episode in iTunes, and it's
    already been downloaded thousands of times. I'll email you a link to
    the file if you are still having problems.

  • dakezhang

    Got it, thx a lot!

  • zelo

    In the episode 66 some listener asked about the research made on a possible therapy to excise HIV form the cell genome. As far as I know so far there has been a successful experiment in which an evolved Cre recombinase (Tre) was developed to recognize the HIV-1 LTRs and excise the DNA sequence in between. The evolved Tre recombinase was tested in human cultured cells (HeLa cells) which had been transfected with a reporter gene (luciferase) within a sequence flanked by the HIV-1 LTRs. Still, as you mentioned in your reply one of the difficulties to overcome would be to selectively target those cells with the HIV provirus in their genome as in a number of cells the virus can remain latent for years. The other serious obstacle is how to introduce in the body enough enzyme or expression vector to successfully reach most infected cells while keeping under control the negative side effects caused by such invasive therapy.
    For those interested in the experiments carried out to develop and test the Tre recombinase, this is the reference of the article in which the results were published:
    Sarkar et al. HIV-1 proviral DNA excision using an evolved recombinase. Science (2007) vol. 316 (5833) pp. 1912
    In that issue a short introduction commenting the experiments was also published:
    Engelman. AIDS/HIV: A Reversal of Fortune in HIV-1 Integration. Science (2007) vol. 316 (5833) pp. 1855

  • Pingback: Unexpected endogenous viruses