Faculty Opinions recommendation of Residual body removal during spermatogenesis in C. elegans requires genes that mediate cell corpse clearance.

Author(s):  
W Brent Derry ◽  
Benjamin Lant
Development ◽  
2012 ◽  
Vol 139 (24) ◽  
pp. 4613-4622 ◽  
Author(s):  
J. Huang ◽  
H. Wang ◽  
Y. Chen ◽  
X. Wang ◽  
H. Zhang

2012 ◽  
Vol 125 (24) ◽  
pp. e1-e1
Author(s):  
J. Huang ◽  
H. Wang ◽  
Y. Chen ◽  
X. Wang ◽  
H. Zhang

2019 ◽  
Vol 218 (8) ◽  
pp. 2619-2637 ◽  
Author(s):  
Qiwen Gan ◽  
Xin Wang ◽  
Qian Zhang ◽  
Qiuyuan Yin ◽  
Youli Jian ◽  
...  

Phagocytic removal of apoptotic cells involves formation, maturation, and digestion of cell corpse–containing phagosomes. The retrieval of lysosomal components following phagolysosomal digestion of cell corpses remains poorly understood. Here we reveal that the amino acid transporter SLC-36.1 is essential for lysosome reformation during cell corpse clearance in Caenorhabditis elegans embryos. Loss of slc-36.1 leads to formation of phagolysosomal vacuoles arising from cell corpse–containing phagosomes. In the absence of slc-36.1, phagosome maturation is not affected, but the retrieval of lysosomal components is inhibited. Moreover, loss of PPK-3, the C. elegans homologue of the PtdIns3P 5-kinase PIKfyve, similarly causes accumulation of phagolysosomal vacuoles that are defective in phagocytic lysosome reformation. SLC-36.1 and PPK-3 function in the same genetic pathway, and they directly interact with one another. In addition, loss of slc-36.1 and ppk-3 causes strong defects in autophagic lysosome reformation in adult animals. Our findings thus suggest that the PPK-3–SLC-36.1 axis plays a central role in both phagocytic and autophagic lysosome formation.


Development ◽  
2011 ◽  
Vol 138 (10) ◽  
pp. 2003-2014 ◽  
Author(s):  
L. J. Neukomm ◽  
A.-S. Nicot ◽  
J. M. Kinchen ◽  
J. Almendinger ◽  
S. M. Pinto ◽  
...  

2014 ◽  
Vol 21 (6) ◽  
pp. 845-853 ◽  
Author(s):  
L J Neukomm ◽  
S Zeng ◽  
A P Frei ◽  
P A Huegli ◽  
M O Hengartner

Autophagy ◽  
2012 ◽  
Vol 8 (8) ◽  
pp. 1267-1268 ◽  
Author(s):  
Wei Zou ◽  
Xiaochen Wang ◽  
Ronald Vale ◽  
Guangshuo Ou

Development ◽  
2001 ◽  
Vol 128 (22) ◽  
pp. 4475-4488 ◽  
Author(s):  
Erik A. Lundquist ◽  
Peter W. Reddien ◽  
Erika Hartwieg ◽  
H. Robert Horvitz ◽  
Cornelia I. Bargmann

The Caenorhabditis elegans genome contains three rac-like genes, ced-10, mig-2, and rac-2. We report that ced-10, mig-2 and rac-2 act redundantly in axon pathfinding: inactivating one gene had little effect, but inactivating two or more genes perturbed both axon outgrowth and guidance. mig-2 and ced-10 also have redundant functions in some cell migrations. By contrast, ced-10 is uniquely required for cell-corpse phagocytosis, and mig-2 and rac-2 have only subtle roles in this process. Rac activators are also used differentially. The UNC-73 Trio Rac GTP exchange factor affected all Rac pathways in axon pathfinding and cell migration but did not affect cell-corpse phagocytosis. CED-5 DOCK180, which acts with CED-10 Rac in cell-corpse phagocytosis, acted with MIG-2 but not CED-10 in axon pathfinding. Thus, distinct regulatory proteins modulate Rac activation and function in different developmental processes.


2017 ◽  
Vol 428 (1) ◽  
pp. 215-223 ◽  
Author(s):  
Dou Wu ◽  
Yongping Chai ◽  
Zhiwen Zhu ◽  
Wenjing Li ◽  
Guangshuo Ou ◽  
...  

2007 ◽  
Vol 15 (1) ◽  
pp. 192-201 ◽  
Author(s):  
S-Y Park ◽  
M-Y Jung ◽  
H-J Kim ◽  
S-J Lee ◽  
S-Y Kim ◽  
...  

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