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. 2008 Dec;22(12):4126–4135. doi: 10.1096/fj.08-112326

TABLE 1.

Oligonucleotides employed in these studies

Oligonucleotide Sequence
Primers for amplification of miR-377 targets on 3′-UTRsa
 P-miR-377 (left) ACAAAAGTTGCCTTTGTGTGAT
 P-control (left) ACAAATGTAGCGTTAGTCTGTT
 P-oligo-dT (right) TTTTTTTTTTTTTTTTTTTT
qPCR primers
 P-actin (left) AGCCATGTACGTAGCCATCC
 P-actin (right) CTCTCAGCTGTGGTGGTGAA
 P-18S rRNA (left) ATGGCCGTTCTTAGTTGGTG
 P-18S rRNA (right) CGCTGAGCCAGTCAGTGTAG
Primers for ChIP assay
 ChIPmir-377–1 ACACTGTATCCTTGGCAGTGG
 ChIPmir-377–2 GCGGGATTTGGTACTGAAAA
 ChIPmir-377–3 AGGGAAAGGTCAAGGTCAGAA
 ChIPmir-377–4 GGGCAGATGGCTACATATTCT
Probes for in situ hybridizationa
 Probe-miR-377 ACAAAAGTTGCCTTTGTGTGAT
 Probe-control ACAAATGTAGCGTTAGTCTGTT
siRNA
 SOD1 UGAUUGGGAUUGCGCAGUAUU
GGACAAAUUACAGGAUUAAUU
GCAGGGAACCAUCCACUUCUU
AAGAGAGGCAUGUUGGAGAUU
 PAK1 AAGAAGACCUCCAAUAGUAUU
GUAUAUACGAUCUGUGAUU
GAUUGGAGCCGGCAGCAAAUU
CGAAGAAAGAGCUGAUUAUUU
 PPM1A ACAAUAGACUGAACCCUUAUU
UCACCAAUAACCAGGAUUUUU
ACACGGCUGUGAUCGGUUUUU
GCAAGCGGAAUGUAAUUGAUU
PcDNA constructs
 PC-miR-377 (forward) TGCTGAGCAGAGGTTGCCCTTGGTGAATTCGCTTTATTTATGTTGAATCACACAAAGGCAACTTTTGTT
 PC-miR-377 (reverse) CCTGAACAAAAGTTGCCTTTGTGTGATTCAACATAAATAAAGCGAATTCACCAAGGGCAACCTCTGCTC
 PC-miR-337 (forward) TCGAGAAGTTGGGGGGTGGGAACGGCGTCATGCAGGAGTTGATTGCACAGCCATTCAGCTCCTATATGATGCCTTTCTTCACCCCCTTCAA
 PC-miR-337 (reverse) GATCTTGAAGGGGGTGAAGAAAGGCATCATATAGGAGCTGAATGGCTGTGCAATCAACTCCTGCATGACGCCGTTCCCACCCCCCAACTTC
a

Underscores indicate “locked” nucleotides.