Fig. S4
- ID
- ZDB-FIG-120209-24
- Publication
- Zhang et al., 2012 - Zebrafish Models for Dyskeratosis Congenita Reveal Critical Roles of p53 Activation Contributing to Hematopoietic Defects through RNA Processing
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Deficiencies of both dkc1 and nola1 lead to the defects of rRNA processing. (A) Schematic figure modified from previous report [29] shows the overview of rRNA processing. (B) A significant decrease of a precursor strand generating ITS1 and 18 S rRNA was detected in the lanes probed with ITS1 in both dkc1 morphant and nola1 mutant compared with wild type controls (arrows in a and b). The total amount of 18 S rRNA was reduced significantly as shown in the lanes probed with 18 S rRNA probe. The intensity of staining of 18 S rRNA relative to the background was measured using ImageJ program. In contrast, no obvious difference was detected in the lanes probed with ITS2 probe. |