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Progress on cell lineage analysis in Drosophila melanogaster

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  • Shanghai Key Laboratory for Signaling and Diseases Research, School of Life Science and Technology, Tongji University, Shanghai 200092, China

Received date: 2011-11-23

  Revised date: 2011-12-30

  Online published: 2012-07-25

Abstract

Lineage analysis of a single cell provides a powerful mean to delineate its functions during animal development, which, however, has been hindered by the complex nature of tissues that consist of many different types of cells with divergent morphologies, structures and functions. Mosaic technique and various labeling methods have provided ideal genetic tools for such studies. In this review, we described seven lineage analysis techniques that have been generally applied in Drosophila melanogaster, including FRT-mediated mitotic recombination, MARCM (Mosaic analysis with a repressible cell marker), TSG (Twin spot generator), Twin-spot MARCM, Q-MARCM (Q system-based MARCM), Cou-pled MARCM, and G-TRACE (Gal4 technique for real-time and clonal expression). These techniques enable researchers to perform genetic manipulations at a single cell level, and trace its development in complicated systems such as the nervous system. These methods may also be applied to lineage analysis in other model organisms.

Cite this article

ZHANG Shi-Ping, XUE Lei . Progress on cell lineage analysis in Drosophila melanogaster[J]. Hereditas(Beijing), 2012 , 34(7) : 819 -828 . DOI: 10.3724/SP.J.1005.2012.00819

References

[1] Luo LQ, Zong H. Single neuron labeling and genetic manipulation. Nat Neurosci, 2001, 4(Suppl.): 1158-1159.
[2] Blair SS. Engrailed expression in the anterior lineage compartment of the developing wing blade of Drosophila. Development, 1992, 115(1): 21-33.
[3] Xu T, Rubin GM. Analysis of genetic mosaics in developing and adult Drosophila tissues. Development, 1993, 117(4): 1223-1237.
[4] Stern C. Somatic crossing over and segregation in Drosophila melanogaster. Genetics, 1936, 21(6): 625-730.
[5] Broach JR, Hicks JB. Replication and recombination functions associated with the yeast plasmid, 2μ circle. Cell, 1980, 21(2): 501-508.
[6] Golic KG, Lindquist S. The FLP recombinase of yeast catalyzes site-specific recombination in the Drosophila genome. Cell, 1989, 59(3): 499-509.
[7] Blair SS. Genetic mosaic techniques for studying Drosophila development. Development, 2003, 130(21): 5065-5072.
[8] Lee T, Luo LQ. Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morpho-genesis. Neuron, 1999, 22(3): 451-461.
[9] Brand AH, Perrimon N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development, 1993, 118(2): 401-415.
[10] Ma J, Ptashne M. The carboxy-terminal 30 amino acids of GAL4 are recognized by GAL80. Cell, 1987, 50(1): 137-142.
[11] Lee T, Luo LQ. Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development. Trends Neurosci, 2001, 24(5): 251-254.
[12] Griffin R, Sustar A, Bonvin M, Binari R, del Valle Rodriguez A, Hohl AM, Bateman JR, Villalta C, Heffern E, Grunwald D, Bakal C, Desplan C, Schubiger G, Wu CT, Perrimon N. The twin spot generator for differential Drosophila lineage analysis. Nat Methods, 2009, 6(8): 600- 602.
[13] Zong H, Espinosa JS, Su HH, Muzumdar MD, Luo LQ. Mosaic analysis with double markers in mice. Cell, 2005, 121(3): 479-492.
[14] Campbell RE, Tour O, Palmer AE, Steinbach PA, Baird GS, Zacharias DA, Tsien RY. A monomeric red fluores-cent protein. Proc Natl Acad Sci USA, 2002, 99(12): 7877-7882.
[15] Cormack BP, Valdivia RH, Falkow S. FACS-optimized mutants of the green fluorescent protein (GFP). Gene, 1996, 173(1): 33-38.
[16] Lai SL, Awasaki T, Ito K, Lee T. Clonal analysis of Drosophila antennal lobe neurons: diverse neu-ronal architectures in the lateral neuroblast lineage. Development, 2008, 135(17): 2883-2893.
[17] Jefferis GSXE, Marin EC, Stocker RF, Luo LQ. Target neuron prespecification in the olfactory map of Drosophila. Nature, 2001, 414(6860): 204-208.
[18] Lee T. New genetic tools for cell lineage analysis in Drosophila. Nat Methods, 2009, 6(8): 566-568.
[19] Yu HH, Chen CH, Shi L, Huang YL, Lee T. Twinspot MARCM to reveal the developmental origin and identity of neurons. Nat Neurosci, 2009, 12(7): 947-953.
[20] Potter CJ, Tasic B, Russler EV, Liang L, Luo LQ. The Q system: a repressible binary system for transgene expression, lineage tracing, and mosaic analysis. Cell, 2010, 141(3): 536-548.
[21] Potter CJ, Luo LQ. Using the Q system in Drosophila melanogaster. Nat Protoc, 2011, 6(8): 1105-1120.
[22] Struhl G, Basler K. Organizing activity of wingless protein in Drosophila. Cell, 1993, 72(4): 527-540.
[23] Evans CJ, Olson JM, Ngo KT, Kim E, Lee NE, Kuoy E, Patananan AN, Sitz D, Tran P, Do MT, Yackle K, Ces-pedes A, Hartenstein V, Call GB, Banerjee U. G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila. Nat Methods, 2009, 6(8): 603-605.
[24] Pastrana E. A toolset for the proficient geneticist. Nat Methods, 2010, 7(7): 488-489.
[25] Bate M. The development of Drosophila melanogaster. New York: Cold Spr
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