3.9 Article

Automated Genome-Wide Visual Profiling of Cellular Proteins Involved in HIV Infection

期刊

JOURNAL OF BIOMOLECULAR SCREENING
卷 16, 期 9, 页码 945-958

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/1087057111415521

关键词

cell-based assays; chip technology and methods; RNA interference; RNAi; shRNA; high-content screening; image analysis

资金

  1. Institut Pasteur Korea
  2. Korean Ministry of Science and Technology
  3. Agence Nationale de Recherche sur le SIDA (ANRS)
  4. Sidaction
  5. CNRS
  6. European Community [201412]
  7. Institut Pasteur

向作者/读者索取更多资源

Recent genome-wide RNAi screens have identified >842 human genes that affect the human immunodeficiency virus (HIV) cycle. The list of genes implicated in infection differs between screens, and there is minimal overlap. A reason for this variance is the interdependence of HIV infection and host cell function, producing a multitude of indirect or pleiotropic cellular effects affecting the viral infection during RNAi screening. To overcome this, the authors devised a 15-dimensional phenotypic profile to define the viral infection block induced by CD4 silencing in HeLa cells. They demonstrate that this phenotypic profile excludes nonspecific, RNAi-based side effects and viral replication defects mediated by silencing of housekeeping genes. To achieve statistical robustness, the authors used automatically annotated RNAi arrays for seven independent genome-wide RNAi screens. This identified 56 host genes, which reliably reproduced CD4-like phenotypes upon HIV infection. The factors include 11 known HIV interactors and 45 factors previously not associated with HIV infection. As proof of concept, the authors confirmed that silencing of PAK1, Ku70, and RNAseH2A impaired HIV replication in Jurkat cells. In summary, multidimensional, visual profiling can identify genes required for HIV infection. (Journal of Biomolecular Screening 2011; 16: 945-958)

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