TBC1D5-Catalyzed Cycling of Rab7 Is Required for Retromer-Mediated Human Papillomavirus Trafficking during Virus Entry

During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selec...

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Published inCell reports (Cambridge) Vol. 31; no. 10; p. 107750
Main Authors Xie, Jian, Heim, Erin N., Crite, Mac, DiMaio, Daniel
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 09.06.2020
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Online AccessGet full text
ISSN2211-1247
2639-1856
2211-1247
DOI10.1016/j.celrep.2020.107750

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Abstract During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selected artificial proteins that modulate cellular proteins required for HPV infection and discovered that entry requires TBC1D5, a retromer-associated, Rab7-specific GTPase-activating protein. Binding of retromer to the HPV L2 capsid protein recruits TBC1D5 to retromer at the endosome membrane, which then stimulates hydrolysis of Rab7-GTP to drive retromer disassembly from HPV and delivery of HPV to the retrograde pathway. Although the cellular retromer cargos CIMPR and DMT1-II require only GTP-bound Rab7 for trafficking, HPV trafficking requires cycling between GTP- and GDP-bound Rab7. Thus, ongoing cargo-induced membrane recruitment, assembly, and disassembly of retromer complexes drive HPV trafficking. [Display omitted] •Traptamer screening identifies TBC1D5 as a human papillomavirus entry factor•TBC1D5 is a Rab7 GTPase-activating protein that activates retromer during HPV entry•Rab7 cycling between GTP- and GDP-bound forms is required for HPV entry•HPV trafficking displays different Rab7 requirements than cellular cargo Xie et al. designed a protein interference screen that identified TBC1D5 as a cellular protein required for HPV entry. TBC1D5 stimulates the GTPase activity of Rab7, which is required for retromer to deliver HPV to the retrograde transport pathway for trafficking of incoming HPV to the nucleus.
AbstractList During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selected artificial proteins that modulate cellular proteins required for HPV infection and discovered that entry requires TBC1D5, a retromer-associated, Rab7-specific GTPase-activating protein. Binding of retromer to the HPV L2 capsid protein recruits TBC1D5 to retromer at the endosome membrane, which then stimulates hydrolysis of Rab7-GTP to drive retromer disassembly from HPV and delivery of HPV to the retrograde pathway. Although the cellular retromer cargos CIMPR and DMT1-II require only GTP-bound Rab7 for trafficking, HPV trafficking requires cycling between GTP- and GDP-bound Rab7. Thus, ongoing cargo-induced membrane recruitment, assembly, and disassembly of retromer complexes drive HPV trafficking. Xie et al. designed a protein interference screen that identified TBC1D5 as a cellular protein required for HPV entry. TBC1D5 stimulates the GTPase activity of Rab7, which is required for retromer to deliver HPV to the retrograde transport pathway for trafficking of incoming HPV to the nucleus.
During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selected artificial proteins that modulate cellular proteins required for HPV infection and discovered that entry requires TBC1D5, a retromer-associated, Rab7-specific GTPase-activating protein. Binding of retromer to the HPV L2 capsid protein recruits TBC1D5 to retromer at the endosome membrane, which then stimulates hydrolysis of Rab7-GTP to drive retromer disassembly from HPV and delivery of HPV to the retrograde pathway. Although the cellular retromer cargos CIMPR and DMT1-II require only GTP-bound Rab7 for trafficking, HPV trafficking requires cycling between GTP- and GDP-bound Rab7. Thus, ongoing cargo-induced membrane recruitment, assembly, and disassembly of retromer complexes drive HPV trafficking. [Display omitted] •Traptamer screening identifies TBC1D5 as a human papillomavirus entry factor•TBC1D5 is a Rab7 GTPase-activating protein that activates retromer during HPV entry•Rab7 cycling between GTP- and GDP-bound forms is required for HPV entry•HPV trafficking displays different Rab7 requirements than cellular cargo Xie et al. designed a protein interference screen that identified TBC1D5 as a cellular protein required for HPV entry. TBC1D5 stimulates the GTPase activity of Rab7, which is required for retromer to deliver HPV to the retrograde transport pathway for trafficking of incoming HPV to the nucleus.
During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selected artificial proteins that modulate cellular proteins required for HPV infection and discovered that entry requires TBC1D5, a retromer-associated, Rab7-specific GTPase-activating protein. Binding of retromer to the HPV L2 capsid protein recruits TBC1D5 to retromer at the endosome membrane, which then stimulates hydrolysis of Rab7-GTP to drive retromer disassembly from HPV and delivery of HPV to the retrograde pathway. Although the cellular retromer cargos CIMPR and DMT1-II require only GTP-bound Rab7 for trafficking, HPV trafficking requires cycling between GTP- and GDP-bound Rab7. Thus, ongoing cargo-induced membrane recruitment, assembly, and disassembly of retromer complexes drive HPV trafficking.During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selected artificial proteins that modulate cellular proteins required for HPV infection and discovered that entry requires TBC1D5, a retromer-associated, Rab7-specific GTPase-activating protein. Binding of retromer to the HPV L2 capsid protein recruits TBC1D5 to retromer at the endosome membrane, which then stimulates hydrolysis of Rab7-GTP to drive retromer disassembly from HPV and delivery of HPV to the retrograde pathway. Although the cellular retromer cargos CIMPR and DMT1-II require only GTP-bound Rab7 for trafficking, HPV trafficking requires cycling between GTP- and GDP-bound Rab7. Thus, ongoing cargo-induced membrane recruitment, assembly, and disassembly of retromer complexes drive HPV trafficking.
During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic from the endosome to downstream cellular compartments, but regulation of retromer activity during HPV entry is poorly understood. Here we selected artificial proteins that modulate cellular proteins required for HPV infection and discovered that entry requires TBC1D5, a retromer-associated, Rab7-specific GTPase-activating protein. Binding of retromer to the HPV L2 capsid protein recruits TBC1D5 to retromer at the endosome membrane, which then stimulates hydrolysis of Rab7-GTP to drive retromer disassembly from HPV and delivery of HPV to the retrograde pathway. Although the cellular retromer cargos CIMPR and DMT1-II require only GTP-bound Rab7 for trafficking, HPV trafficking requires cycling between GTP- and GDP-bound Rab7. Thus, ongoing cargo-induced membrane recruitment, assembly, and disassembly of retromer complexes drive HPV trafficking.
ArticleNumber 107750
Author Heim, Erin N.
DiMaio, Daniel
Crite, Mac
Xie, Jian
AuthorAffiliation 1 Department of Genetics, Yale School of Medicine, PO Box 208005, New Haven, CT 06520-8005, USA
3 Department of Therapeutic Radiology, Yale School of Medicine, PO Box 208040, New Haven, CT 06520-8040, USA
5 Yale Cancer Center, PO Box 208028, New Haven, CT 06520-8028, USA
2 Department of Microbial Pathogenesis, Yale School of Medicine, 295 Congress Avenue, New Haven, CT 06519, USA
6 Lead Contact
4 Department of Molecular Biophysics & Biochemistry, Yale School of Medicine, PO Box 208024, New Haven, CT 06520-8024, USA
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– name: 4 Department of Molecular Biophysics & Biochemistry, Yale School of Medicine, PO Box 208024, New Haven, CT 06520-8024, USA
– name: 6 Lead Contact
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Issue 10
Keywords senescence
traptamer
retromer
retrograde
TBC1D5
functional genetics screen
proximity ligation assay
Rab7B
HPV
Language English
License This is an open access article under the CC BY license.
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Conceptualization, J.X., E.N.H., and D.D.; Data Curation, J.X. and M.C.; Funding Acquisition, M.C. and D.D.; Investigation, J.X. and M.C.; Methodology, J.X., E.N.H., and M.C.; Project Administration, D.D.; Supervision, D.D.; Visualization, J.X., M.C., and D.D.; Writing – Original Draft, J.X.
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Snippet During virus entry, human papillomaviruses are sorted by the cellular trafficking complex, called retromer, into the retrograde transport pathway to traffic...
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StartPage 107750
SubjectTerms Alphapapillomavirus - metabolism
Alphapapillomavirus - physiology
Cell Line
functional genetics screen
GTPase-Activating Proteins - metabolism
HEK293 Cells
HeLa Cells
HPV
Humans
Keratinocytes
Papillomavirus Infections - metabolism
Papillomavirus Infections - virology
Protein Transport
proximity ligation assay
rab GTP-Binding Proteins - metabolism
rab7 GTP-Binding Proteins
Rab7B
retrograde
retromer
senescence
TBC1D5
traptamer
Vesicular Transport Proteins - metabolism
Virus Internalization
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Title TBC1D5-Catalyzed Cycling of Rab7 Is Required for Retromer-Mediated Human Papillomavirus Trafficking during Virus Entry
URI https://dx.doi.org/10.1016/j.celrep.2020.107750
https://www.ncbi.nlm.nih.gov/pubmed/32521275
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https://pubmed.ncbi.nlm.nih.gov/PMC7339955
http://www.cell.com/article/S2211124720307300/pdf
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