Identification of Tissue-Specific MicroRNAs from Mouse

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Identification of Tissue-Specific MicroRNAs from Mouse Mariana Lagos-Quintana, Reinhard Rauhut, Abdullah Yalcin, Jutta Meyer, Winfried Lendeckel, Thomas Tuschl Current Biology Volume 12, Issue 9, Pages 735-739 (April 2002) DOI: 10.1016/S0960-9822(02)00809-6

Figure 1 Northern Blot Analysis of Tissue-Specific miRNAs Total RNA from different mouse tissues was blotted and probed with a 5′-radiolabeled oligodeoxynucleotide complementary to the indicated miRNA. Equal loading of total RNA on the gel was verified by ethidium bromide staining prior to transfer; the band representing tRNAs is shown. The foldback precursors are indicated with capital “L.” Mouse brains were dissected into midbrain (mb), cortex (cx), and cerebellum (cb). The rest of the brain (rb) was also used. Other tissues were heart (ht), lung (lg), liver (lv), colon (co), small intestine (si), pancreas (pc), spleen (sp), kidney (kd), skeletal muscle (sm), stomach (st); H, human HeLa SS3 cells. Current Biology 2002 12, 735-739DOI: (10.1016/S0960-9822(02)00809-6)

Figure 2 Potential Orthologs of lin-4 stRNA (A) Sequence alignment of C. elegans lin-4 stRNA with mouse miR-125a and miR-125b and the D. melanogaster miR-125. Differences are highlighted by gray boxes. (B) Northern blot of total RNA isolated from staged populations of D. melanogaster, probed for miR-125. E, embryo; L, larval stage; P, pupae; A, adult; S2, Schneider-2 cells. Current Biology 2002 12, 735-739DOI: (10.1016/S0960-9822(02)00809-6)