Clonal analyss Clones have been created by ey FLusng the FLFRT technque.Snce ey FLcanduce clones the eye antennal dsc prmordum pror to ts segregatonto eye and antennal felds, t canduce clones each the eye and antennal dsc.stat92E clones had been produced usng FRT82B ub GFnls 3R TM6B, Tb.Mnute clones were produced by FRT82B M 96C arm lacZ.upd orhoexpressng flout clones were generated usng UAS upd or UAShoand the flout cassette stock 25 T2,hs flMKRS TM6B, whch FLs kinase inhibitor Decitabine beneath the control of theheat shock promoter.Flout clones express each Upd orhoand GFP.Tmed collectonsw or GMR upd fles were growvals at 25 C.For tmed collectons, we allowed the fles to lay eggs for 2hours.The embryos have been mantaned at 25 C unt 110hours right after egg deposton, whch corresponds to md thrd nstar.At ths tme, we solated GFnegatve larvae, whch signify GMR upd anmals.1 of your par of eye dscs a sngle larva was takefor RNA solaton.Another was fxed 50% glutaraldehyde, mounted oa mcroscope slde and vsually nspected by brghtfeld mcroscopy for the morphogenetc furrowhavng progressed approxmatelyhalf way throughout the eye dsc.
RNA solatoFor each mcro array, complete RNA was extracted from a sngle md thrd nstar larval eye dsc read the full info here usng the Arcturus solatokt.The RNA qualty and quantty was assessed usng the Agent 2100 Boanalyzer and NanodroND one thousand, and subsequently amplfed usng the Arcturus Amplfcatokt.Labeled ant sense RNA was syntheszed from the resultng cDNA usng the ENZO BoArrayhgheld RNA Transcrpt Labelng Kt.Right after solatoand amplfcaton, the aRNA was agaassayed through the Agent 2100 Boanalyzer and NanodroND 1000.Mcro array information acqustoand analyss Equal amounts of amplfed manage and GMR upd aRNA had been separatelyhybrdzed onto the GeneChpR Drosopha Genome two.0 Arrays.The chprocessng and mage acqustowere obtaned followng the recommendatons within the array producer.The raw data were normalzed usng Model Based Expressondex and further ftered usng GeneSprng seven.two.
To dentfy the dfferentally abundant mRNAs betweethe two groups, the pre processed information have been rgorously statstcally ftered by check as well as by Sgnfcance Analyss

of Mcro array at False Dscovery Charge set to 10%.from the resultng gene lsts had been performed usng a world wide web based mostly device DAVD bonformatcs assets.Prmary data from ths studyhas beedeposted at NCB GEO database.Quanttatve true tme PCR We performed Q PCR for valdatoof potental canddate genes usng the SYBR GreePCR Mx protocol and a authentic tme PCR machne from Appled Bosystems.We solated and amplfed the RNA usng precisely the same kts and protocols as the ones applied for that mcro array.We measured the cDNA concentratousng a NanodroND 1000.We implemented three ng of cDNA per sample per reacton, five uM of each prmer and 1X SYBR.