Table 2.
Minor satellite | Major satellite | X141 | |
WT (OS25) | 0.4 ± 0.1 | 1.8 ± 0.5 | 1.8 ± 0.3 |
Eed KO | 7.2 ± 6.5† | 18.5 ± 17.0† | 1.8 ± 0.2 |
Dnmt1 KO | 0.3 ± 0.1 | 2.1 ± 0.0 | 2.0 ± 1.3 |
Dnmt3a/3b DKO | 0.1 ± 0.0 | 5.7 ± 2.4 | 1.5 ± 0.9 |
G9a WT | 0.1 ± 0.0 | 0.7 ± 0.1 | 0.5 ± 0.7 |
G9a KO | 0.4 ± 0.4 | 1.0 ± 0.2 | ND |
Suv39 h1/h2 WT | 4.9 ± 0.8 | 2.5 ± 1. 6 | 1.1 ± 0.3 |
Suv39 h1/h2 DKO | 4.0 ± 1.3 | 2.2 ± 0.7 | 2.1 ± 0.5 |
Dicer WT | 0.2 ± 0.0 | 4.1 ± 0.0 | 2.7 ± 0.0 |
Dicer KO | 0.9 ± 0.6 | 17.4 ± 5.5 | 4.1 ± 1.2 |
C2C12 dif | 100 | 100 | 100 |
*Levels of repeat sequence RNA were normalized to a house keeping gene (Ube) and expressed as a percentage of the levels detected in differentiated mouse myocytes derived from C2C12 (C2C12 dif), samples in which high levels of major and minor satellite transcripts have previously been detected [56]. Controls without reverse transcriptase were analyzed in parallel to dismiss contamination with genomic DNA.
†Four independent samples showed variable but increased transcript levels: major satellite, 8.2%, 8.7%, 13.4%, and 43.8% of C2C12; minor satellite, 2.6%, 7.1%, 11.8%, and 13.8% of C2C12. ND, none detected.