scholarly journals Importin α1 is required for maintaining germline stem cells in Drosophila melanogaster testes

2017 ◽  
Vol 145 ◽  
pp. S163-S164
Author(s):  
James Heaney ◽  
Franca Casagranda ◽  
Gary Hime
2019 ◽  
Vol 31 ◽  
pp. 14-19 ◽  
Author(s):  
Yuto Yoshinari ◽  
Yoshitomo Kurogi ◽  
Tomotsune Ameku ◽  
Ryusuke Niwa

2009 ◽  
Vol 88 (7) ◽  
pp. 397-408 ◽  
Author(s):  
Phillip Karpowicz ◽  
Milena Pellikka ◽  
Evelyn Chea ◽  
Dorothea Godt ◽  
Ulrich Tepass ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Ryo Hoshino ◽  
Ryusuke Niwa

In many insect species, mating stimuli can lead to changes in various behavioral and physiological responses, including feeding, mating refusal, egg-laying behavior, energy demand, and organ remodeling, which are collectively known as the post-mating response. Recently, an increase in germline stem cells (GSCs) has been identified as a new post-mating response in both males and females of the fruit fly, Drosophila melanogaster. We have extensively studied mating-induced increase in female GSCs of D. melanogaster at the molecular, cellular, and systemic levels. After mating, the male seminal fluid peptide [e.g. sex peptide (SP)] is transferred to the female uterus. This is followed by binding to the sex peptide receptor (SPR), which evokes post-mating responses, including increase in number of female GSCs. Downstream of SP-SPR signaling, the following three hormones and neurotransmitters have been found to act on female GSC niche cells to regulate mating-induced increase in female GSCs: (1) neuropeptide F, a peptide hormone produced in enteroendocrine cells; (2) octopamine, a monoaminergic neurotransmitter synthesized in ovary-projecting neurons; and (3) ecdysone, a steroid hormone produced in ovarian follicular cells. These humoral factors are secreted from each organ and are received by ovarian somatic cells and regulate the strength of niche signaling in female GSCs. This review provides an overview of the latest findings on the inter-organ relationship to regulate mating-induced female GSC increase in D. melanogaster as a model. We also discuss the remaining issues that should be addressed in the future.


Biology Open ◽  
2014 ◽  
Vol 3 (6) ◽  
pp. 510-521 ◽  
Author(s):  
B. Herzig ◽  
T. A. Yakulov ◽  
K. Klinge ◽  
U. Gunesdogan ◽  
H. Jackle ◽  
...  

2020 ◽  
Author(s):  
Manashree Malpe ◽  
Cordula Schulz

SUMMARYThe replenishment of specialized cells depends on the activity of stem cells. Recent advances in stem cell research have shown that the germline stem cells (GSCs) in Drosophila melanogaster can increase their mitotic activity in response to mating. Here, we show that this ability to respond to mating is eliminated if the males are mutant for the ABC transporter, White, the genetic background for a plethora of fly lines. Furthermore, we were not able to reproduce previous findings that female flies increase their GSC numbers and mitotic activity upon mating. Our findings underline the importance of careful experimental design and control specimen.


2015 ◽  
Vol 5 (4) ◽  
pp. 583-592 ◽  
Author(s):  
Heather A. Flores ◽  
Vanessa L. Bauer DuMont ◽  
Aalya Fatoo ◽  
Diana Hubbard ◽  
Mohammed Hijji ◽  
...  

Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 245-256
Author(s):  
Kirsteen Munn ◽  
Ruth Steward

Abstract In Drosophila melanogaster, the process of oogenesis is initiated with the asymmetric division of a germline stem cell. This division results in the self-renewal of the stem cell and the generation of a daughter cell that undergoes four successive mitotic divisions to produce a germline cyst of 16 cells. Here, we show that shut-down is essential for the normal function of the germline stem cells. Analysis of weak loss-of-function alleles confirms that shut-down is also required at later stages of oogenesis. Clonal analysis indicates that shut-down functions autonomously in the germline. Using a positional cloning approach, we have isolated the shut-down gene. Consistent with its function, the RNA and protein are strongly expressed in the germline stem cells and in 16-cell cysts. The RNA is also present in the germ cells throughout embryogenesis. shut-down encodes a novel Drosophila protein similar to the heat-shock protein-binding immunophilins. Like immunophilins, Shut-down contains an FK506-binding protein domain and a tetratricopeptide repeat. In plants, high-molecular-weight immunophilins have been shown to regulate cell divisions in the root meristem in response to extracellular signals. Our results suggest that shut-down may regulate germ cell divisions in the germarium.


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