Figure 3.
Pri-miRNAs lacking a CPA signal are retained in chromatin, whereas ENE-containing pri-miRNAs are released. (A) Schematic of primers used for PCR in B and C. (B and C) Nuclear location of pri-miRNAs. Cells transfected with constructs diagramed in Fig. 2 A for pri-let-7 (B) or pri-lin-4 (C) were fractionated into released, nucleoplasmic RNAs (supernatant [S]) and chromatin-associated RNAs (pellet [P]). Fractionated RNA was reverse transcribed and amplified by PCR. β-actin pre-mRNA and spliced mRNA were amplified as controls for fractionation efficiency.