miR-544 Regulates Dairy Goat Male Germline Stem Cell Self-Renewal via Targeting PLZF

2015 ◽  
Vol 116 (10) ◽  
pp. 2155-2165 ◽  
Author(s):  
Wencong Song ◽  
Hailong Mu ◽  
Jiang Wu ◽  
Mingzhi Liao ◽  
Haijing Zhu ◽  
...  
2015 ◽  
Vol 117 (4) ◽  
pp. 844-852 ◽  
Author(s):  
Hailong Mu ◽  
Na Li ◽  
Jiang Wu ◽  
Liming Zheng ◽  
Yuanxin Zhai ◽  
...  

2013 ◽  
Vol 46 (2) ◽  
pp. 223-231 ◽  
Author(s):  
M. Li ◽  
M. Yu ◽  
C. Liu ◽  
H. Zhu ◽  
X. He ◽  
...  

2009 ◽  
Vol 185 (4) ◽  
pp. 613-627 ◽  
Author(s):  
Akos Szakmary ◽  
Mary Reedy ◽  
Hongying Qi ◽  
Haifan Lin

Yb regulates the proliferation of both germline and somatic stem cells in the Drosophila melanogaster ovary by activating piwi and hh expression in niche cells. In this study, we show that Yb protein is localized as discrete cytoplasmic spots exclusively in the somatic cells of the ovary and testis. These spots, which are different from all known cytoplasmic structures in D. melanogaster, are evenly electron-dense spheres 1.5 µm in diameter (herein termed the Yb body). The Yb body is frequently associated with mitochondria and a less electron-dense sphere of similar size that appears to be RNA rich. There are one to two Yb bodies/cell, often located close to germline cells. The N-terminal region of Yb is required for hh expression in niche cells, whereas the C-terminal region is required for localization to Yb bodies. The entire Yb protein is necessary for piwi expression in niche cells. A double mutant of Yb and a novel locus show male germline loss, revealing a function for Yb in male germline stem cell maintenance.


eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Cuie Chen ◽  
Mayu Inaba ◽  
Zsolt G Venkei ◽  
Yukiko M Yamashita

Asymmetric stem cell division is often accompanied by stereotypical inheritance of the mother and daughter centrosomes. However, it remains unknown whether and how stem cell centrosomes are uniquely regulated and how this regulation may contribute to stem cell fate. Here we identify Klp10A, a microtubule-depolymerizing kinesin of the kinesin-13 family, as the first protein enriched in the stem cell centrosome in Drosophila male germline stem cells (GSCs). Depletion of klp10A results in abnormal elongation of the mother centrosomes in GSCs, suggesting the existence of a stem cell-specific centrosome regulation program. Concomitant with mother centrosome elongation, GSCs form asymmetric spindle, wherein the elongated mother centrosome organizes considerably larger half spindle than the other. This leads to asymmetric cell size, yielding a smaller differentiating daughter cell. We propose that klp10A functions to counteract undesirable asymmetries that may result as a by-product of achieving asymmetries essential for successful stem cell divisions.


2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Jin Sun ◽  
Hui-Min Wei ◽  
Jiang Xu ◽  
Jian-Feng Chang ◽  
Zhihao Yang ◽  
...  

Science ◽  
2012 ◽  
Vol 338 (6107) ◽  
pp. 679-682 ◽  
Author(s):  
V. Tran ◽  
C. Lim ◽  
J. Xie ◽  
X. Chen

2012 ◽  
Vol 2 (3) ◽  
pp. 343-351 ◽  
Author(s):  
Yalan Xing ◽  
Irina Kurtz ◽  
Manisha Thuparani ◽  
Jillian Legard ◽  
Hannele Ruohola-Baker

2012 ◽  
Vol 23 (8) ◽  
pp. 1524-1532 ◽  
Author(s):  
Therese M. Roth ◽  
C.-Y. Ason Chiang ◽  
Mayu Inaba ◽  
Hebao Yuan ◽  
Viktoria Salzmann ◽  
...  

Drosophila male germline stem cells (GSCs) divide asymmetrically, balancing self-renewal and differentiation. Although asymmetric stem cell division balances between self-renewal and differentiation, it does not dictate how frequently differentiating cells must be produced. In male GSCs, asymmetric GSC division is achieved by stereotyped positioning of the centrosome with respect to the stem cell niche. Recently we showed that the centrosome orientation checkpoint monitors the correct centrosome orientation to ensure an asymmetric outcome of the GSC division. When GSC centrosomes are not correctly oriented with respect to the niche, GSC cell cycle is arrested/delayed until the correct centrosome orientation is reacquired. Here we show that induction of centrosome misorientation upon culture in poor nutrient conditions mediates slowing of GSC cell proliferation via activation of the centrosome orientation checkpoint. Consistently, inactivation of the centrosome orientation checkpoint leads to lack of cell cycle slowdown even under poor nutrient conditions. We propose that centrosome misorientation serves as a mediator that transduces nutrient information into stem cell proliferation, providing a previously unappreciated mechanism of stem cell regulation in response to nutrient conditions.


Genetics ◽  
2010 ◽  
Vol 186 (2) ◽  
pp. 573-583 ◽  
Author(s):  
Tora K. Smulders-Srinivasan ◽  
Akos Szakmary ◽  
Haifan Lin

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