The Ribosome Assembly Factor LSG1 Interacts with Vesicle-Associated Membrane Protein-Associated Proteins (VAPs)

LSG1 is a conserved GTPase involved in ribosome assembly. It is required for the eviction of the nuclear export adapter NMD3 from the pre-60S subunit in the cytoplasm. In human cells, LSG1 has also been shown to interact with vesicle-associated membrane protein-associated proteins (VAPs) that are found primarily on the endoplasmic reticulum. VAPs interact with a large host of proteins which contain FFAT motifs (two phenylalanines (FF) in an acidic tract) and are involved in many cellular functions including membrane traffic and regulation of lipid transport. Here, we show that human LSG1 binds to VAPs via a noncanonical FFAT-like motif. Deletion of this motif specifically disrupts the localization of LSG1 to the ER, without perturbing LSG1-dependent recycling of NMD3 <i>in cells</i> or modulation of LSG1 GTPase activity <i>in vitro</i>.

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Publication Details

Journal
Molecular and Cellular Biology
Published
2024-08-12
DOI
https://doi.org/10.1080/10985549.2024.2384600
Citations
2
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.47
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article

The Ribosome Assembly Factor LSG1 Interacts with Vesicle-Associated Membrane Protein-Associated Proteins (VAPs)

Sharmishtha Musalgaonkar, Blerta Xhemalçe, Putri Sutjita, Jeffrey Recchia-Rife et al.
2 citations
Molecular and Cellular Biology
RNA and protein synthesis mechanisms
0.47
article

The Ribosome Assembly Factor LSG1 Interacts with Vesicle-Associated Membrane Protein-Associated Proteins (VAPs)

Sharmishtha Musalgaonkar, Blerta Xhemalçe, Putri Sutjita, Jeffrey Recchia-Rife, L. K. Huang, Alan M. Johnson
article en
2 citations

Abstract

LSG1 is a conserved GTPase involved in ribosome assembly. It is required for the eviction of the nuclear export adapter NMD3 from the pre-60S subunit in the cytoplasm. In human cells, LSG1 has also been shown to interact with vesicle-associated membrane protein-associated proteins (VAPs) that are found primarily on the endoplasmic reticulum. VAPs interact with a large host of proteins which contain FFAT motifs (two phenylalanines (FF) in an acidic tract) and are involved in many cellular functions including membrane traffic and regulation of lipid transport. Here, we show that human LSG1 binds to VAPs via a noncanonical FFAT-like motif. Deletion of this motif specifically disrupts the localization of LSG1 to the ER, without perturbing LSG1-dependent recycling of NMD3 <i>in cells</i> or modulation of LSG1 GTPase activity <i>in vitro</i>.

Molecular and Cellular BiologyVol. 44(9)
The University of Texas at Austin (US)
Openalex Percentile: Top 36%
RNA and protein synthesis mechanisms
0.47
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