A role for Rab30 in retrograde trafficking and maintenance of endosome-TGN organization

2021 ◽  
pp. 112442
Author(s):  
Khalisah L. Zulkefli ◽  
Ismail S. Mahmoud ◽  
Nicholas A. Williamson ◽  
Prajakta Kulkarni Gosavi ◽  
Fiona J. Houghton ◽  
...  
2017 ◽  
Vol 216 (7) ◽  
pp. 1887-1889 ◽  
Author(s):  
Jakob B. Sørensen

The functions of four of the five proteins in the mammalian uncoordinated-13 (Munc13) family have been identified as priming factors in SNARE-dependent exocytosis. In this issue, Zhang et al. (2017. J. Cell Biol. https://doi.org/10.1083/jcb.201702099) show that the fifth member, BAIAP3 (brain-specific angiogenesis inhibitor I–associated protein 3), acts in retrograde trafficking by returning secretory vesicle material to the trans-Golgi network. In its absence, secretory vesicle formation is impaired, leading to accumulation of immature vesicles, or lysosomal vesicle degradation.


Science ◽  
2012 ◽  
Vol 338 (6109) ◽  
pp. 963-967 ◽  
Author(s):  
K. McGourty ◽  
T. L. Thurston ◽  
S. A. Matthews ◽  
L. Pinaud ◽  
L. J. Mota ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Harriet Crawley-Snowdon ◽  
Ji-Chun Yang ◽  
Nathan R. Zaccai ◽  
Luther J. Davis ◽  
Lena Wartosch ◽  
...  

Abstract VARP and TBC1D5 are accessory/regulatory proteins of retromer-mediated retrograde trafficking from endosomes. Using an NMR/X-ray approach, we determined the structure of the complex between retromer subunit VPS29 and a 12 residue, four-cysteine/Zn++ microdomain, which we term a Zn-fingernail, two of which are present in VARP. Mutations that abolish VPS29:VARP binding inhibit trafficking from endosomes to the cell surface. We show that VARP and TBC1D5 bind the same site on VPS29 and can compete for binding VPS29 in vivo. The relative disposition of VPS29s in hetero-hexameric, membrane-attached, retromer arches indicates that VARP will prefer binding to assembled retromer coats through simultaneous binding of two VPS29s. The TBC1D5:VPS29 interaction is over one billion years old but the Zn-fingernail appears only in VARP homologues in the lineage directly giving rise to animals at which point the retromer/VARP/TBC1D5 regulatory network became fully established.


2020 ◽  
Vol 65 ◽  
pp. 112-121 ◽  
Author(s):  
Massiullah Shafaq-Zadah ◽  
Estelle Dransart ◽  
Ludger Johannes

Viruses ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 483
Author(s):  
Gianfranco Pietrantoni ◽  
Rodrigo Ibarra-Karmy ◽  
Gloria Arriagada

Following entry into the host cell, retroviruses generate a dsDNA copy of their genomes via reverse transcription, and this viral DNA is subsequently integrated into the chromosomal DNA of the host cell. Before integration can occur, however, retroviral DNA must be transported to the nucleus as part of a ‘preintegration complex’ (PIC). Transporting the PIC through the crowded environment of the cytoplasm is challenging, and retroviruses have evolved different mechanisms to accomplish this feat. Within a eukaryotic cell, microtubules act as the roads, while the microtubule-associated proteins dynein and kinesin are the vehicles that viruses exploit to achieve retrograde and anterograde trafficking. This review will examine the various mechanisms retroviruses have evolved in order to achieve retrograde trafficking, confirming that each retrovirus has its own strategy to functionally subvert microtubule associated proteins.


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