{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T19:44:56Z","timestamp":1791315896459,"version":"4.3.1"},"reference-count":138,"publisher":"The Royal Society","issue":"1517","license":[{"start":{"date-parts":[[2008,11,27]],"date-time":"2008-11-27T00:00:00Z","timestamp":1227744000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/royalsociety.org\/journals\/ethics-policies\/data-sharing-mining\/"}],"content-domain":{"domain":["royalsocietypublishing.org"],"crossmark-restriction":true},"short-container-title":["Phil. Trans. R. Soc. B"],"published-print":{"date-parts":[[2009,3,12]]},"abstract":"<jats:p>\n                    Members of the APOBEC family of cellular polynucleotide cytidine deaminases, most notably APOBEC3G and APOBEC3F, are potent inhibitors of HIV-1 infection. Wild type HIV-1 infections are largely spared from APOBEC3G\/F function through the action of the essential viral protein, Vif. In the absence of Vif, APOBEC3G\/F are encapsidated by budding virus particles leading to excessive cytidine (C) to uridine (U) editing of negative sense reverse transcripts in newly infected cells. This registers as guanosine (G) to adenosine (A) hypermutations in plus-stranded cDNA. In addition to this profoundly debilitating effect on genetic integrity, APOBEC3G\/F also appear to inhibit viral DNA synthesis by impeding the translocation of reverse transcriptase along template RNA. Because the functions of Vif and APOBEC3G\/F proteins oppose each other, it is likely that fluctuations in the Vif\u2013APOBEC balance may influence the natural history of HIV-1 infection, as well as viral sequence diversification and evolution. Given Vif's critical role in suppressing APOBEC3G\/F function, it can be argued that pharmacologic strategies aimed at restoring the activity of these intrinsic anti-viral factors in the context of infected cells\n                    <jats:italic>in vivo<\/jats:italic>\n                    have clear therapeutic merit, and therefore deserve aggressive pursuit.\n                  <\/jats:p>","DOI":"10.1098\/rstb.2008.0185","type":"journal-article","created":{"date-parts":[[2008,11,27]],"date-time":"2008-11-27T21:01:15Z","timestamp":1227819675000},"page":"675-687","update-policy":"https:\/\/doi.org\/10.1098\/crossmark-policy","source":"Crossref","is-referenced-by-count":250,"title":["APOBEC proteins and intrinsic resistance to HIV-1 infection"],"prefix":"10.1098","volume":"364","author":[{"given":"Michael H","family":"Malim","sequence":"first","affiliation":[{"name":"Department of Infectious Diseases, King's College London School of Medicine2nd Floor, Borough Wing, Guy's Hospital, London Bridge, London SE1 9RT, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"175","published-online":{"date-parts":[[2008,11,27]]},"reference":[{"key":"e_1_3_2_2_1","doi-asserted-by":"publisher","DOI":"10.1128\/JVI.78.20.11070-11076.2004"},{"key":"e_1_3_2_3_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.0030019"},{"key":"e_1_3_2_4_1","doi-asserted-by":"publisher","DOI":"10.1097\/00041433-200104000-00009"},{"key":"e_1_3_2_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.virol.2008.01.042"},{"key":"e_1_3_2_6_1","doi-asserted-by":"publisher","DOI":"10.1006\/jmbi.1994.1018"},{"key":"e_1_3_2_7_1","doi-asserted-by":"publisher","DOI":"10.1086\/511988"},{"key":"e_1_3_2_8_1","doi-asserted-by":"publisher","DOI":"10.1038\/ni1125"},{"key":"e_1_3_2_9_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.cub.2004.06.057"},{"key":"e_1_3_2_10_1","doi-asserted-by":"publisher","DOI":"10.1126\/science.1100658"},{"key":"e_1_3_2_11_1","doi-asserted-by":"publisher","DOI":"10.1128\/JVI.00839-06"},{"key":"e_1_3_2_12_1","unstructured":"Bishop K. 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