{"title":"Secondary structure of the HIV‑1 genome","authors":"J. D. Stephenson, A. Lever","doi":"10.2217/HIV.09.44","DOIUrl":null,"url":null,"abstract":"Evaluation of: Watts JM, Dang KK, Gorelick RJ: Architecture and secondary structure of an entire HIV-1 RNA genome. Nature 460(6), 711–716 (2009). The ssRNA, comprising the HIV genome, present as a doublet in HIV-1, has the ability of all RNA molecules to fold using Watson–Crick and noncanonical base pairing to form helices and loops, which are themselves functional as protein- and RNA-binding sites that regulate many stages of the viral lifecycle. This article explores the ability of a single technique (SHAPE) to map these structures in full length HIV RNA and attempts to suggest functions associated with these structures. The demonstration of a novel rapid technique that can generate extensive base by base data is an important achievement and it is useful to see this technique being publicized. This well-presented article is an attractive showpiece for the capabilities of SHAPE. However, some of the data are ambiguous and some are subject to alternative interpretations. SHAPE is a useful additional rapid...","PeriodicalId":88510,"journal":{"name":"HIV therapy","volume":"11 1","pages":"557-563"},"PeriodicalIF":0.0000,"publicationDate":"2009-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"HIV therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2217/HIV.09.44","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
Abstract
Evaluation of: Watts JM, Dang KK, Gorelick RJ: Architecture and secondary structure of an entire HIV-1 RNA genome. Nature 460(6), 711–716 (2009). The ssRNA, comprising the HIV genome, present as a doublet in HIV-1, has the ability of all RNA molecules to fold using Watson–Crick and noncanonical base pairing to form helices and loops, which are themselves functional as protein- and RNA-binding sites that regulate many stages of the viral lifecycle. This article explores the ability of a single technique (SHAPE) to map these structures in full length HIV RNA and attempts to suggest functions associated with these structures. The demonstration of a novel rapid technique that can generate extensive base by base data is an important achievement and it is useful to see this technique being publicized. This well-presented article is an attractive showpiece for the capabilities of SHAPE. However, some of the data are ambiguous and some are subject to alternative interpretations. SHAPE is a useful additional rapid...