scholarly journals Non-autonomous regulation of germline stem cell proliferation by somatic MPK-1/MAPK activity in C. elegans

Cell Reports ◽  
2021 ◽  
Vol 35 (8) ◽  
pp. 109162
Author(s):  
Sarah Robinson-Thiewes ◽  
Benjamin Dufour ◽  
Pier-Olivier Martel ◽  
Xavier Lechasseur ◽  
Amani Ange Danielle Brou ◽  
...  
Author(s):  
Sarah Robinson-Thiewes ◽  
Benjamin Dufour ◽  
Pier-Olivier Martel ◽  
Xavier Lechasseur ◽  
Amani Ange Danielle Brou ◽  
...  

AbstractExtracellular signal-regulated kinase (ERK)/mitogen-activated protein kinase (MAPK) is a major positive regulator of cell proliferation that is often upregulated in cancer. Yet few studies have addressed ERK/MAPK regulation of proliferation within a complete organism. The C. elegans ERK/MAPK ortholog MPK-1 is best known for its control of somatic organogenesis and germline differentiation, but it also stimulates germline stem cell proliferation. Here we identify tissue-specific MPK-1 isoforms and characterize their distinct roles in germline function. The germline-specific MPK-1B isoform promotes germline differentiation, but has no apparent role in germline stem cell proliferation. By contrast, the soma-specific MPK-1A isoform promotes germline proliferation non-autonomously. Indeed, MPK-1A functions in the intestine or somatic gonad to promote germline proliferation, independently of its other known roles. We propose that a non-autonomous role of ERK/MAPK in stem cell proliferation may be conserved across species and other tissue types, with major clinical implications for cancer and other diseases.


Development ◽  
2021 ◽  
Vol 148 (15) ◽  
Author(s):  
Kumari Pushpa ◽  
Sunayana Dagar ◽  
Harsh Kumar ◽  
Diksha Pathak ◽  
Sivaram V. S. Mylavarapu

ABSTRACT The conserved exocyst complex regulates plasma membrane-directed vesicle fusion in eukaryotes. However, its role in stem cell proliferation has not been reported. Germline stem cell (GSC) proliferation in the nematode Caenorhabditis elegans is regulated by conserved Notch signaling. Here, we reveal that the exocyst complex regulates C. elegans GSC proliferation by modulating Notch signaling cell autonomously. Notch membrane density is asymmetrically maintained on GSCs. Knockdown of exocyst complex subunits or of the exocyst-interacting GTPases Rab5 and Rab11 leads to Notch redistribution from the GSC-niche interface to the cytoplasm, suggesting defects in plasma membrane Notch deposition. The anterior polarity (aPar) protein Par6 is required for GSC proliferation, and for maintaining niche-facing membrane levels of Notch and the exocyst complex. The exocyst complex biochemically interacts with the aPar regulator Par5 (14-3-3ζ) and Notch in C. elegans and human cells. Exocyst components are required for Notch plasma membrane localization and signaling in mammalian cells. Our study uncovers a possibly conserved requirement of the exocyst complex in regulating GSC proliferation and in maintaining optimal membrane Notch levels.


2016 ◽  
Vol 38 (1) ◽  
pp. 33-46 ◽  
Author(s):  
Snehal N. Chaudhari ◽  
Madhumati Mukherjee ◽  
Alexandra S. Vagasi ◽  
Gaofeng Bi ◽  
Mohammad M. Rahman ◽  
...  

Science ◽  
2011 ◽  
Vol 334 (6058) ◽  
pp. 990-992 ◽  
Author(s):  
E. M. Fast ◽  
M. E. Toomey ◽  
K. Panaram ◽  
D. Desjardins ◽  
E. D. Kolaczyk ◽  
...  

2015 ◽  
Vol 117 (4) ◽  
pp. 844-852 ◽  
Author(s):  
Hailong Mu ◽  
Na Li ◽  
Jiang Wu ◽  
Liming Zheng ◽  
Yuanxin Zhai ◽  
...  

PLoS Biology ◽  
2018 ◽  
Vol 16 (9) ◽  
pp. e2005004 ◽  
Author(s):  
Tomotsune Ameku ◽  
Yuto Yoshinari ◽  
Michael J. Texada ◽  
Shu Kondo ◽  
Kotaro Amezawa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document