Figure 5.
Figure 5. Inhibition of DNA methylation results in reactivation of IgH transcription. (A) Map of the VH region showing the location of primers used for RT-PCR analysis of IgH expression. Location of the forward primer in the leader regions enables the discrimination between spliced mRNA and genomic DNA contamination. V indicates variable; D, diversity; and J, joining. (B) Detection of Ig transcription in cHL cells by RT-PCR. L428, L1236, and KM-H2 cells were incubated for 72 hours in the presence of the indicated concentrations of 5-aza-dC. Total RNA was extracted from 1 × 106 cells and converted to cDNA. The specifically amplified products were detected by ethidium bromide staining on agarose gels. Sizes of the PCR products are indicated in Table 1.

Inhibition of DNA methylation results in reactivation of IgH transcription. (A) Map of the VH region showing the location of primers used for RT-PCR analysis of IgH expression. Location of the forward primer in the leader regions enables the discrimination between spliced mRNA and genomic DNA contamination. V indicates variable; D, diversity; and J, joining. (B) Detection of Ig transcription in cHL cells by RT-PCR. L428, L1236, and KM-H2 cells were incubated for 72 hours in the presence of the indicated concentrations of 5-aza-dC. Total RNA was extracted from 1 × 106 cells and converted to cDNA. The specifically amplified products were detected by ethidium bromide staining on agarose gels. Sizes of the PCR products are indicated in Table 1.

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