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Cited by 570

The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.

RETROVIRUS BUDDING

Morita, Eiji, Sundquist, Wesley I.·2004·Annual Review of Cell and Developmental Biology

Abstract

▪ Abstract Human immunodeficiency virus (HIV) and other retroviruses acquire their envelopes and spread infection by budding through the limiting membranes of producer cells. To facilitate budding, retroviruses usurp a cellular pathway that is normally used to create vesicles that bud into late endosomal compartments called multivesicular bodies (MVB). Research on yeast and human MVB biogenesis has led to the identification of ∼25 human proteins that are required for vesicle formation and for HIV-1 budding, and has produced a working model for sequential recruitment of these proteins during MVB vesicle formation. Retroviruses can redirect this machinery to the plasma membrane and leave the cell in a single step or, alternatively, can bud directly into MVB compartments and then exit cells via the exosome pathway. Remarkably, virus release from both the plasma membrane and MVB compartments can occur directionally into specialized sites of cell-to-cell contact called virological synapses. Thus retroviruses have evolved elaborate mechanisms for escaping the cell and maximizing their chances of infecting a new host.

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Crossref · 10.1146/annurev.cellbio.20.010403.102350

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Metadata

Authors
Morita, E., & Sundquist, W. I.
Venue
Annual Review of Cell and Developmental Biology
Published
2004-11-01
Volume
20
Issue
1
Pages
395-425
ISSN
  • 1081-0706 (ISSN-L)
  • 1530-8995
OpenAlex
W4249167162
Cited by
570
References
13
FWCI
3.22
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: RETROVIRUS BUDDING. https://app.cochat.ai/papers/10.1146/annurev.cellbio.20.010403.102350
The paper
Morita, E., & Sundquist, W. I. (2004). RETROVIRUS BUDDING. Annual Review of Cell and Developmental Biology. https://doi.org/10.1146/annurev.cellbio.20.010403.102350

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.