Lineage tracing quantification reveals symmetric stem cell division in drosophila male germline stem cells

Cellular and Molecular Bioengineering

Volumn 6, Issue 4, 2013, Pages 441-448

  Salzmann, Viktoria ^a   Inaba, Mayu ^a   Cheng, Jun ^b   Yamashita, Yukiko M ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b University of Illinois at Chicago   (United States)

Author keywords

Asymmetric division; Dedifferentiation; Drosophila; Niche; Stem cells

Indexed keywords

MOESIN; UVOMORULIN;

ANIMAL CELL; ARTICLE; CELL DIVISION; CELL FUNCTION; CONTROLLED STUDY; DROSOPHILA MELANOGASTER; GERM CELL; GERMLINE STEM CELL; MALE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; TESTIS;

DROSOPHILA MELANOGASTER;

EID: 84890311421     PISSN: 18655025     EISSN: 18655033     Source Type: Journal    
DOI: 10.1007/s12195-013-0295-6     Document Type: Article

References (25)

1. Ameres, S. L., and P. D. Zamore. Diversifying microRNA sequence and function. Nat. Rev. Mol. Cell Biol. 14(8):475-488, 2013. doi: 10.1038/nrm3611.
2. Aravin, A. A., R. Sachidanandam, A. Girard, K. Fejes-Toth, and G. J. Hannon. Developmentally regulated piRNA clusters implicate MILI in transposon control. Science 316:744-747, 2007. doi: 10.1126/science.1142612.
3. Boyle, M., C. Wong, M. Rocha, and D. L. Jones. Decline in self-renewal factors contributes to aging of the stem cell niche in the Drosophila testis. Cell Stem Cell 1:470-478, 2007.
4. Brawley, C., and E. Matunis. Regeneration of male germline stem cells by spermatogonial dedifferentiation in vivo. Science 304:1331-1334, 2004.
5. Cheng, J., et al. Centrosome misorientation reduces stem cell division during ageing. Nature 456:599-604, 2008.
6. Jin, Z., et al. Differentiation-defective stem cells outcompete normal stem cells for niche occupancy in the Drosophila ovary. Cell Stem Cell 2:39-49, 2008.
7. Kai, T., and A. Spradling. Differentiating germ cells can revert into functional stem cells in Drosophila melanogaster ovaries. Nature 428:564-569, 2004.
8. Kiger, A. A., D. L. Jones, C. Schulz, M. B. Rogers, and M. T. Fuller. Stem cell self-renewal specified by JAK-STAT activation in response to a support cell cue. Science 294:2542-2545, 2001.
9. Klein, A. M., T. Nakagawa, R. Ichikawa, S. Yoshida, and B. D. Simons. Mouse germ line stem cells undergo rapid and stochastic turnover. Cell Stem Cell 7:214-224, 2010. doi: 10.1016/j.stem.2010.05.017.
10. Leatherman, J. L., and S. Dinardo. Zfh-1 controls somatic stem cell self-renewal in the Drosophila testis and nonautonomously influences germline stem cell self-renewal. Cell Stem Cell 3:44-54, 2008.
11. Leatherman, J. L., and S. Dinardo. Germline self-renewal requires cyst stem cells and stat regulates niche adhesion in Drosophila testes. Nat. Cell Biol. 12:806-811, 2010. doi: 10.1038/ncb2086.
12. Li, C., et al. Collapse of germline piRNAs in the absence of Argonaute3 reveals somatic piRNAs in flies. Cell 137:509-521, 2009. doi: 10.1016/j.cell.2009.04.027.
13. Minestrini, G., A. S. Harley, and D. M. Glover. Localization of Pavarotti-KLP in living Drosophila embryos suggests roles in reorganizing the cortical cytoskeleton during the mitotic cycle. Mol. Biol. Cell 14:4028-4038, 2003.
14. Nakagawa, T., Y. Nabeshima, and S. Yoshida. Functional identification of the actual and potential stem cell compartments in mouse spermatogenesis. Dev. Cell 12:195-206, 2007.
15. Nakagawa, T., M. Sharma, Y. Nabeshima, R. E. Braun, and S. Yoshida. Functional hierarchy and reversibility within the murine spermatogenic stem cell compartment. Science 328:62-67, 2010. doi: 10.1126/science.1182868.
16. Rogers, G. C., et al. Two mitotic kinesins cooperate to drive sister chromatid separation during anaphase. Nature 427:364-370, 2004. doi: 10.1038/nature02256.
17. Sheng, X. R., C. M. Brawley, and E. L. Matunis. Dedifferentiating spermatogonia outcompete somatic stem cells for niche occupancy in the Drosophila testis. Cell Stem Cell 5:191-203, 2009. doi: 10.1016/j.stem.2009.05. 024.
18. Sheng, X. R., and E. Matunis. Live imaging of the Drosophila spermatogonial stem cell niche reveals novel mechanisms regulating germline stem cell output. Development 138:3367-3376, 2011. doi: 10.1242/dev.065797.
19. Snippert, H. J., et al. Intestinal crypt homeostasis results from neutral competition between symmetrically dividing Lgr5 stem cells. Cell 143:134-144, 2010. doi: 10.1016/j.cell.2010.09.016.
20. Tulina, N., and E. Matunis. Control of stem cell self-renewal in Drosophila spermatogenesis by JAK-STAT signaling. Science 294:2546-2549, 2001.
21. Wallenfang, M. R., R. Nayak, and S. DiNardo. Dynamics of the male germline stem cell population during aging of Drosophila melanogaster. Aging Cell 5:297-304, 2006.
22. Yadlapalli, S., J. Cheng, and Y. M. Yamashita. Drosophila male germline stem cells do not asymmetrically segregate chromosome strands. J. Cell Sci. 124:933-939, 2011. doi: 10.1242/jcs.079798.
23. Yadlapalli, S., and Y. M. Yamashita. Chromosome-specific nonrandom sister chromatid segregation during stem-cell division. Nature 498(7453):251-254, 2013. doi: 10.1038/nature12106.
24. Yamashita, Y. M., D. L. Jones, and M. T. Fuller. Orientation of asymmetric stem cell division by the APC tumor suppressor and centrosome. Science 301:1547-1550, 2003.
25. Yamashita, Y. M., A. P. Mahowald, J. R. Perlin, and M. T. Fuller. Asymmetric inheritance of mother versus daughter centrosome in stem cell division. Science 315:518-521, 2007.