Figure 6.

Steady-state mRNA levels at two convergent transcription units in wild-type and DCL2KO cells. (A) and (B) Total RNA was prepared from wild-type and dcl2−/− cells and analyzed by Northern hybridization with a probe specific for the genes indicated below the read distribution. See additional file 3 for sequences of the hybridization probes. The hybridization was quantitated by PhosphorImager analysis, normalized to the loading control (tRNA) and expressed as a ratio between dcl2−/− and wt.

Tschudi et al. BMC Genomics 2012 13:427   doi:10.1186/1471-2164-13-427
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