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Files in this Data Supplement:
Fig. S1. Broad low-level expression of Sens in AWM and PWM before the precursors of the mechanosensory and the PWM bristle are selected. (A-A″) Double-staining of an A101-lacZ pupal wing at 2 hours APF for β-Gal (green) and Sens (red). Anterior is to the left. At this stage, the AWM chemosensory pIs are selected and co-express high levels of Sens and β-Gal. Two bands of low-level Sens expression persist along the WM.
Fig. S2. Sens is expressed in PWM bristle precursors. (A-A″) Close-up of the PWM of an 8- to 10-hour APF A101-lacZ pupa stained for β-Gal (green) and Sens (red). Sens expression is refined to single cells in the two rows of PWM precursors (compare with Fig. S1). Sens and β-Gal colocalize in these precursors.
Fig. S3. Overexpression of the anti-apoptotic protein P35 does not rescue the sens mutant phenotype in WM mechanosensory organs. (A) A MARCM sens clone that overexpresses P35. Note that the bristle loss is not rescued. (B,B′) Close-up view of the AWM of a 24- to 30-hour APF pupa with a MARCM sens clone overexpressing P35. Nuclear GFP (blue) marks the mutant tissue. Note that none of the sens mutant cells express Elav (red).
Fig. S4. Overexpression of da is able to induce high levels of Sens in single cells in the absence of the ASC. (A-A′) A MARCM Df(1)sc-B57 clone in the thorax (green) expressing da under the control of Eq-GAL4, stained with anti-Sens (red) and anti-Da (green) antibodies. Da staining identifies the ASC clone. Note that similar to the wild-type tissue, Sens accumulates in single cells, the presumptive pI cells, upon overexpression of da in ASC clones.
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