Figure 1.
Identification and characterization of circMYBL2 in FLT3-ITD+ AML. (A) Identification of circRNAs having significant differences (P < .01) in FLT3-ITD+ AML compared with FLT3-ITD– AML. (B) Differential expression of circMYBL2 between FLT3-ITD+ and FLT3-ITD– AML patient samples. (C) Structures of the MYBL2 genome and transcript. circMYBL2 is produced by exons 8-9. (D) Identity of the junction point of circMYBL2. (E) RNase R treatment confirmed the circular form of circMYBL2. (F-G) Identification of circMYBL2 cytoplasmic distribution by qRT-PCR analysis and FISH. MTOC1 and MALAT1 were used as the cytoplasmic and nuclear markers, respectively. Cy3 dye and DAPI stain; original magnification ×63. DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.

Identification and characterization of circMYBL2 in FLT3-ITD+ AML. (A) Identification of circRNAs having significant differences (P < .01) in FLT3-ITD+ AML compared with FLT3-ITD AML. (B) Differential expression of circMYBL2 between FLT3-ITD+ and FLT3-ITD AML patient samples. (C) Structures of the MYBL2 genome and transcript. circMYBL2 is produced by exons 8-9. (D) Identity of the junction point of circMYBL2. (E) RNase R treatment confirmed the circular form of circMYBL2. (F-G) Identification of circMYBL2 cytoplasmic distribution by qRT-PCR analysis and FISH. MTOC1 and MALAT1 were used as the cytoplasmic and nuclear markers, respectively. Cy3 dye and DAPI stain; original magnification ×63. DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.

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