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<pubDate>Thu, 21 Aug 2008 09:43:19 BST</pubDate>


	<title>CiteULike: kieran101's library [249 articles]</title>
	<description>CiteULike: kieran101's library [249 articles]</description>


	<link>http://www.citeulike.org/user/kieran101/article/2789377</link>
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    <title>HIV-1 and MLV Gag proteins are sufficient to recruit APOBEC3G into virus-like particles</title>
    <link>http://www.citeulike.org/user/kieran101/article/2789377</link>
    <description>&lt;i&gt;Biochemical and Biophysical Research Communications, Vol. 321, No. 3. (27 August 2004), pp. 566-573.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The cytidine deaminase hAPOBEC3G is an antiviral human factor that counteracts the replication of HIV-1 in absence of the Vif protein. hAPOBEC3G is packaged into virus particles and lethally hypermutates HIV-1. In this work, we examine the mechanisms governing hAPOBEC3G packaging. By GST pull-down and co-immunoprecipitation assays, we show that hAPOBEC3G binds to HIV-1 Pr55 Gag and its NC domain and to the RT and IN domains contained in Pr160 Gag-Pol. We demonstrate that the expression of HIV-1 Gag is sufficient to induce the packaging of hAPOBEC3G into Gag particles. Gag-Pol polypeptides containing RT and IN domains, as well as HIV-1 genomic RNA, seem not to be necessary for hAPOBEC3G packaging. Lastly, we show that hAPOBEC3G and its murine ortholog are packaged into HIV-1 and MLV Gag particles. We conclude that the Gag polypeptides from distant retroviruses have conserved domains allowing the packaging of the host antiviral factor APOBEC3G.</description>
    <dc:title>HIV-1 and MLV Gag proteins are sufficient to recruit APOBEC3G into virus-like particles</dc:title>

    <dc:creator>Marc Douaisi</dc:creator>
    <dc:creator>Sylvie Dussart</dc:creator>
    <dc:creator>Marianne Courcoul</dc:creator>
    <dc:creator>Gilles Bessou</dc:creator>
    <dc:creator>Robert Vigne</dc:creator>
    <dc:creator>Etienne Decroly</dc:creator>
    <dc:identifier>doi:10.1016/j.bbrc.2004.07.005</dc:identifier>
    <dc:source>Biochemical and Biophysical Research Communications, Vol. 321, No. 3. (27 August 2004), pp. 566-573.</dc:source>
    <dc:date>2008-05-12T12:36:25-00:00</dc:date>
    <prism:publicationYear>2004</prism:publicationYear>
    <prism:publicationName>Biochemical and Biophysical Research Communications</prism:publicationName>
    <prism:volume>321</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>566</prism:startingPage>
    <prism:endingPage>573</prism:endingPage>
    <prism:category>apobec</prism:category>
    <prism:category>assembly</prism:category>
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