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Y1v1hoptum fm7c

The Y1v1hopTum/FM7c is a stock of Drosophila melanogaster, the common fruit fly. This stock contains a balancer chromosome, FM7c, which is used to maintain the Y1v1hopTum mutation. The Y1v1hopTum mutation is located on the X chromosome and is associated with the tumor suppressor gene.

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2 protocols using y1v1hoptum fm7c

1

Genetic Fly Lines for Developmental Analysis

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Flies were raised on standard media. Crosses were raised at 25°C unless otherwise noted. 10xstat92E-GFP (BL#26197) [22 (link)], UAS-eGFP (BL#5430), UAS-eGFP (BL#5431), hsflp122;;Ubi-RFP,FRT79 (made from BL#34498), y1v1hopTum/FM7c (BL#8492; referred to as hopTum-l), act5c-GAL4/CyO (BL#4414), UAS-MYR-RFP/CyO (BL#7118), hml-GAL4 (BL#30139) and stat06346 (BL# 11681) were obtained from Bloomington Drosophila Stock Center, Bloomington, IN. UAS-hipkRNAi (VDRC ID#108254, [23 (link)]) was obtained from Vienna Drosophila Resource Center, Vienna, Austria. Also used were dpp-GAL4/TM6B [24 (link)], os,y (a gift from Norbert Perrimon), UAS-Stat92E-GFP/Cyo and UAS-Stat92E-MYC/Cyo,wg-lacZ (a gift from James Castelli-Gair Hombria, [25 (link),26 (link)], PD-lacZ (a gift from Henry Sun; referred to as upd1-lacZ hereon after, Tsai and Sun, 2004 [27 (link)]), ywhsflp,tub-GAL4,UAS-GFP,6X MYC-NLS; UAS-y+;tub-GAL80,FRT2A/TM6B (a gift from Gary Struhl), ywhsflp122;sp/Cyo;TM2/TM6B, UAS-HA-hipk1M, UAS-HA-hipk3M, hipk4,FRT79/TM6B [28 (link)], UAS-HA-hipkWT-attP40, UAS-MYR-HA-hipk-attP40, UAS-NLS-HA-hipk-attP40 (made in this study). act5c-GAL4/CyO and UAS-MYR-RFP/CyO were recombined to generate act5c-GAL4, UAS-MYR-RFP/CyO. hipk4, FRT79/TM6B and 10xstat92E-GFP/TM6B were recombined to generate hipk4, FRT79,10xstat92E-GFP/TM6B.
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2

Drosophila Genetic Manipulation Techniques

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The CG9989 (sid) RNAi line was obtained from the Fly Stocks of National Institute of Genetics (NIG-FLY, Japan). The W1118, y1v1 hopTum/FM7c, and W1118;Df(3R)Exel6209,P{XP-U}Exel6209/TM6B,Tb1 were obtained from Bloomington Drosophila Stock Center at Indiana University. The ubiquitin-GAL4 line was kindly provided by Dr. Utpal Banerjee at University of California, Los Angeles and the UAS-dicer line was obtained from Dr. Kyung-An Han at The University of Texas at El Paso. The UAS-sid line was generated by BestGene (Chino Hills, CA). Additionally, sid knock down and ubiquitous over expression lines were generated using standard genetic methods by crossing of flies carrying the UAS-sid RNAi, UAS-sid, W/Ubiquitin-GAL4;Df(3R)Exel6209,P{XP-U}Exel6209/UAS-sid RNAi, Ubiquitin-GAL4;UAS-sid RNAi, Ubiquitin-GAL4;UAS-sid and Ubiquitin-GAL4;UAS-dicer;UAS-sid RNAi. All flies were maintained in standard corn meal/agar medium (110 g sucrose, 52 g cornmeal, 27.4 g yeast, 7 g agar, 2.4 g methyl p-hydroxybenzoate/8.5 ml ethanol, and 1.5 g propionic acid/L) at 25°C except that the temperature was increased to 29°C during septic infection. Flies were kept in humidified incubators programmed for 12 hour day/night periods.
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