HOW Is Required for Stem Cell Maintenance in the Drosophila Testis and for the Onset of Transit-Amplifying Divisions

被引:37
|
作者
Monk, Adrian C. [1 ,2 ]
Siddall, Nicole A. [1 ,2 ]
Volk, Talila [3 ]
Fraser, Barbara [2 ,4 ]
Quinn, Leonie M. [1 ]
McLaughlin, Eileen A. [2 ,4 ]
Hime, Gary R. [1 ,2 ]
机构
[1] Univ Melbourne, Dept Anat & Cell Biol, Melbourne, Vic 3010, Australia
[2] ARC Ctr Excellence Biotechnol & Dev, Callaghan, NSW 2308, Australia
[3] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[4] Univ Newcastle, Sch Environm & Life Sci, Callaghan, NSW 2308, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
RNA-BINDING PROTEIN; DEVELOPMENTAL REGULATORS; SELF-RENEWAL; ISOFORMS; GERM-CELL; CYCLIN-A; DIFFERENTIATION; SPERMATOGENESIS; PROLIFERATION; DEGRADATION;
D O I
10.1016/j.stem.2010.02.016
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The mechanisms by which germline stem cells (GSCs) in the Drosophila testis undergo asymmetric division to regenerate a stem cell as well as a daughter (gonialblast) that will only undergo a further four mitotic divisions prior to entering premeiotic S phase and differentiating into a cyst of spermatocytes are not fully resolved. Here we demonstrate that the HOW RNA-binding protein is required for maintenance of CycB and therefore mitotic progression in GSCs and gonialblasts as well as determining the timing of the spermatogonial divisions. HOW is normally expressed in a complementary pattern to Barn in the germline and barn mRNA is bound by HOW in vivo. Ectopic expression of the HOW(L) isoform is associated with a delay in accumulation of Barn to the level required for differentiation, resulting in extra mitotic divisions. Spatiotemporal regulation of HOW expression is therefore required to specify the four spermatogonial transit-amplifying divisions.
引用
收藏
页码:348 / 360
页数:13
相关论文
共 50 条
  • [1] Adult stem and transit-amplifying cell location
    Diaz-Flores, L., Jr.
    Madrid, J. F.
    Gutierrez, R.
    Varela, H.
    Valladares, F.
    Alvarez-Arguelles, H.
    Diaz-Flores, L.
    HISTOLOGY AND HISTOPATHOLOGY, 2006, 21 (09) : 995 - 1027
  • [2] Transit-Amplifying Cells Orchestrate Stem Cell Activity and Tissue Regeneration
    Hsu, Ya-Chieh
    Li, Lishi
    Fuchs, Elaine
    CELL, 2014, 157 (04) : 935 - 949
  • [3] CG8005 Mediates Transit-Amplifying Spermatogonial Divisions via Oxidative Stress in Drosophila Testes
    Chen, Wanyin
    Luan, Xiaojin
    Yan, Yidan
    Wang, Min
    Zheng, Qianwen
    Chen, Xia
    Yu, Jun
    Fang, Jie
    OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2020, 2020 (2020)
  • [4] A transit-amplifying population underpins the efficient regenerative capacity of the testis
    Carrieri, Claudia
    Comazzetto, Stefano
    Grover, Amit
    Morgan, Marcos
    Buness, Andreas
    Nerlov, Claus
    O'Carroll, Donal
    JOURNAL OF EXPERIMENTAL MEDICINE, 2017, 214 (06): : 1631 - 1641
  • [5] The regulated elimination of transit-amplifying cells preserves tissue homeostasis during protein starvation in Drosophila testis
    Yang, Heiko
    Yamashita, Yukiko M.
    DEVELOPMENT, 2015, 142 (10): : 1756 - 1766
  • [6] Aging Epidermis Is Maintained by Changes in Transit-Amplifying Cell Kinetics, Not Stem Cell Kinetics
    Winter, Michael C.
    Bickenbach, Jackie R.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (11) : 2541 - 2543
  • [7] CG6015 controls spermatogonia transit-amplifying divisions by epidermal growth factor receptor signaling in Drosophila testes
    Jun Yu
    Qianwen Zheng
    Zhiran Li
    Yunhao Wu
    Yangbo Fu
    Xiaolong Wu
    Dengfeng Lin
    Cong Shen
    Bo Zheng
    Fei Sun
    Cell Death & Disease, 12
  • [8] CG6015 controls spermatogonia transit-amplifying divisions by epidermal growth factor receptor signaling in Drosophila testes
    Yu, Jun
    Zheng, Qianwen
    Li, Zhiran
    Wu, Yunhao
    Fu, Yangbo
    Wu, Xiaolong
    Lin, Dengfeng
    Shen, Cong
    Zheng, Bo
    Sun, Fei
    CELL DEATH & DISEASE, 2021, 12 (05)
  • [9] Regulation of stem cell maintenance and transit amplifying cell proliferation by TGF-β signaling in Drosophila spermatogenesis
    Shivdasani, AA
    Ingham, PW
    CURRENT BIOLOGY, 2003, 13 (23) : 2065 - 2072
  • [10] Could the transit-amplifying stage of stem cell differentiation be the most suited for transplantation purposes?
    Heng, BC
    Cao, T
    MEDICAL HYPOTHESES, 2005, 65 (02) : 412 - 413