spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.



Fig. 6. Mio localizes to oocyte nuclei. (A) Western blot analysis of ovarian protein extracts. The {alpha}Mio antibody recognizes a single band that coincides with the predicted molecular size of Mio, 98.6 kDa in extract from wild type (WT) and the Mio overexpression line (UASp-mio). Additionally, the antibody recognizes a slightly smaller protein (asterisk) in mio2 ovarian extracts. mio2 is predicted to encode a truncated Mio protein of 92.6 kDa. The last lane is a higher contrast picture of the mio2 extract. (B) A wild-type ovariole stained with {alpha}Mio. (C) Faint Mio signal is detected in two cells of a cyst in region 2a. The pattern is often not symmetric, with one nucleus (large arrow) frequently having a brighter signal. In region 2b and region 3, the staining is restricted to a single cell and dramatically increases in intensity (arrows). (D) C(3)G localization in the same germarium as depicted in C. Small box denotes magnified region-2b nucleus stained with {alpha}Mio (red) and {alpha}C(3)G (green). Arrows and arrowheads indicate {alpha}Mio-positive cells in B and {alpha}C(3)G-positive cells in D. E is a diagram showing the stages and localization of Mio (red) and C(3)G (green) in the germarium depicted in C and D. The Mio protein colocalizes to the nuclei that stain most intensely with {alpha}C(3)G in region 2a (large arrowheads and arrows). However, the overlay of a region 2b nucleus demonstrates that the Mio protein has a different distribution than the SC component C(3)G (small box).





Right arrow Return to article