TY - JOUR AB - Clathrin-mediated vesicle trafficking plays central roles in post-Golgi transport. In yeast (Saccharomyces cerevisiae), the AP-1 complex and GGA adaptors are predicted to generate distinct transport vesicles at the trans-Golgi network (TGN), and the epsin-related proteins Ent3p and Ent5p (collectively Ent3p/5p) act as accessories for these adaptors. Recently, we showed that vesicle transport from the TGN is crucial for yeast Rab5 (Vps21p)-mediated endosome formation, and that Ent3p/5p are crucial for this process, whereas AP-1 and GGA adaptors are dispensable. However, these observations were incompatible with previous studies showing that these adaptors are required for Ent3p/5p recruitment to the TGN, and thus the overall mechanism responsible for regulation of Vps21p activity remains ambiguous. Here, we investigated the functional relationships between clathrin adaptors in post-Golgi-mediated Vps21p activation. We show that AP-1 disruption in the ent3Δ5Δ mutant impaired transport of the Vps21p guanine nucleotide exchange factor Vps9p transport to the Vps21p compartment and severely reduced Vps21p activity. Additionally, GGA adaptors, the phosphatidylinositol-4-kinase Pik1p and Rab11 GTPases Ypt31p and Ypt32p were found to have partially overlapping functions for recruitment of AP-1 and Ent3p/5p to the TGN. These findings suggest a distinct role of clathrin adaptors for Vps21p activation in the TGN–endosome trafficking pathway. AU - Nagano, Makoto AU - Aoshima, Kaito AU - Shimamura, Hiroki AU - Siekhaus, Daria E AU - Toshima, Junko Y. AU - Toshima, Jiro ID - 14316 IS - 17 JF - Journal of Cell Science SN - 0021-9533 TI - Distinct role of TGN-resident clathrin adaptors for Vps21p activation in the TGN-endosome trafficking pathway VL - 136 ER - TY - JOUR AB - Although budding yeast has been extensively used as a model organism for studying organelle functions and intracellular vesicle trafficking, whether it possesses an independent endocytic early/sorting compartment that sorts endocytic cargos to the endo-lysosomal pathway or the recycling pathway has long been unclear. The structure and properties of the endocytic early/sorting compartment differ significantly between organisms; in plant cells, the trans-Golgi network (TGN) serves this role, whereas in mammalian cells a separate intracellular structure performs this function. The yeast syntaxin homolog Tlg2p, widely localizing to the TGN and endosomal compartments, is presumed to act as a Q-SNARE for endocytic vesicles, but which compartment is the direct target for endocytic vesicles remained unanswered. Here we demonstrate by high-speed and high-resolution 4D imaging of fluorescently labeled endocytic cargos that the Tlg2p-residing compartment within the TGN functions as the early/sorting compartment. After arriving here, endocytic cargos are recycled to the plasma membrane or transported to the yeast Rab5-residing endosomal compartment through the pathway requiring the clathrin adaptors GGAs. Interestingly, Gga2p predominantly localizes at the Tlg2p-residing compartment, and the deletion of GGAs has little effect on another TGN region where Sec7p is present but suppresses dynamics of the Tlg2-residing early/sorting compartment, indicating that the Tlg2p- and Sec7p-residing regions are discrete entities in the mutant. Thus, the Tlg2p-residing region seems to serve as an early/sorting compartment and function independently of the Sec7p-residing region within the TGN. AU - Toshima, Junko Y. AU - Tsukahara, Ayana AU - Nagano, Makoto AU - Tojima, Takuro AU - Siekhaus, Daria E AU - Nakano, Akihiko AU - Toshima, Jiro ID - 13316 JF - eLife TI - The yeast endocytic early/sorting compartment exists as an independent sub-compartment within the trans-Golgi network VL - 12 ER - TY - JOUR AB - Solute carriers are increasingly recognized as participating in a plethora of pathologies, including cancer. We describe here the involvement of the orphan solute carrier MFSD1 in the regulation of tumor cell migration. Loss of MFSD1 enabled higher levels of metastasis in a mouse model. We identified an increased migratory potential in MFSD1-/- tumor cells which was mediated by increased focal adhesion turn-over, reduced stability of mature inactive β1 integrin, and the resulting increased integrin activation index. We show that MFSD1 promoted recycling to the cell surface of endocytosed inactive β1 integrin and thereby protected β1 integrin from proteolytic degradation; this led to dampening of the integrin activation index. Furthermore, down-regulation of MFSD1 expression was observed during early steps of tumorigenesis and higher MFSD1 expression levels correlate with a better cancer patient prognosis. In sum, we describe a requirement for endolysosomal MFSD1 in efficient β1 integrin recycling to suppress tumor spread. AU - Roblek, Marko AU - Bicher, Julia AU - van Gogh, Merel AU - György, Attila AU - Seeböck, Rita AU - Szulc, Bozena AU - Damme, Markus AU - Olczak, Mariusz AU - Borsig, Lubor AU - Siekhaus, Daria E ID - 10712 JF - Frontiers in Oncology SN - 2234-943X TI - The solute carrier MFSD1 decreases β1 integrin’s activation status and thus tumor metastasis VL - 12 ER - TY - JOUR AB - Ribosomal defects perturb stem cell differentiation, causing diseases called ribosomopathies. How ribosome levels control stem cell differentiation is not fully known. Here, we discovered three RNA helicases are required for ribosome biogenesis and for Drosophila oogenesis. Loss of these helicases, which we named Aramis, Athos and Porthos, lead to aberrant stabilization of p53, cell cycle arrest and stalled GSC differentiation. Unexpectedly, Aramis is required for efficient translation of a cohort of mRNAs containing a 5’-Terminal-Oligo-Pyrimidine (TOP)-motif, including mRNAs that encode ribosomal proteins and a conserved p53 inhibitor, Novel Nucleolar protein 1 (Non1). The TOP-motif co-regulates the translation of growth-related mRNAs in mammals. As in mammals, the La-related protein co-regulates the translation of TOP-motif containing RNAs during Drosophila oogenesis. Thus, a previously unappreciated TOP-motif in Drosophila responds to reduced ribosome biogenesis to co-regulate the translation of ribosomal proteins and a p53 repressor, thus coupling ribosome biogenesis to GSC differentiation. AU - Martin, Elliot T. AU - Blatt, Patrick AU - Ngyuen, Elaine AU - Lahr, Roni AU - Selvam, Sangeetha AU - Yoon, Hyun Ah M. AU - Pocchiari, Tyler AU - Emtenani, Shamsi AU - Siekhaus, Daria E AU - Berman, Andrea AU - Fuchs, Gabriele AU - Rangan, Prashanth ID - 10714 IS - 7 JF - Developmental Cell SN - 1534-5807 TI - A translation control module coordinates germline stem cell differentiation with ribosome biogenesis during Drosophila oogenesis VL - 57 ER - TY - JOUR AB - Cells migrate through crowded microenvironments within tissues during normal development, immune response, and cancer metastasis. Although migration through pores and tracks in the extracellular matrix (ECM) has been well studied, little is known about cellular traversal into confining cell-dense tissues. We find that embryonic tissue invasion by Drosophila macrophages requires division of an epithelial ectodermal cell at the site of entry. Dividing ectodermal cells disassemble ECM attachment formed by integrin-mediated focal adhesions next to mesodermal cells, allowing macrophages to move their nuclei ahead and invade between two immediately adjacent tissues. Invasion efficiency depends on division frequency, but reduction of adhesion strength allows macrophage entry independently of division. This work demonstrates that tissue dynamics can regulate cellular infiltration. AU - Akhmanova, Maria AU - Emtenani, Shamsi AU - Krueger, Daniel AU - György, Attila AU - Pereira Guarda, Mariana AU - Vlasov, Mikhail AU - Vlasov, Fedor AU - Akopian, Andrei AU - Ratheesh, Aparna AU - De Renzis, Stefano AU - Siekhaus, Daria E ID - 10713 IS - 6591 JF - Science SN - 0036-8075 TI - Cell division in tissues enables macrophage infiltration VL - 376 ER -