Table 1.
Primers | DNA sequences |
---|---|
qRT-PCR GnRH sense | 5′ CCCTTTGACTTTCACATCC 3′ |
qRT-PCR GnRH antisense | 5′ GGGTTCTGCCATTTGATCCAC 3′ |
qRT-PCR Otx2 sense | 5′-GCAGAGGTCCTATCCCATGA-3′ (Larder and Mellon, 2009) |
qRT-PCR Otx2 antisense | 5′-CTGGGTGGAAAGAGAAGCTG-3′ (Larder and Mellon, 2009) |
qRT-PCR 18S sense | 5′-TGGTTGATCCTGCCAGTAG-3′ |
qRT-PCR 18S antisense | 5′-CGACCAAAGGAACCATAACT- 3′ |
Otx-2 mutant sense | 5′-GCGAGAATTACCGGCGCCAAAGAACTTTTTCG-3′ |
Otx-2 mutant antisense | 5′-GCTTTTTCAAGAAACCGCGGCCATTAAGAGCG-3′ |
Otx-2 binding site at the KsRE (−3005/−3000 bp) | |
Sense | 5′-CAGAGCTGATGGAAACCACA-3′ |
Antisense | 5′-AGGAAACCACACCCAACAAG-3′ |
Otx-2 binding site at the nKsRE (−2418/−2413 bp) | |
Sense | 5′-GGCTTGATTATAGCCACCAGGAAAGG-3′ |
Antisense | 5′-GACATGCCACTCTCCTGA-3′ |
Otx-2 binding site at the NSE (−319/−252 bp) | |
Sense | 5′-TCCCTGTGAGTTTTTCAGTGTG-3′ |
Antisense | 5′-GCAGCACAGCCCATAGTCTT-3′ |
Negative control primers (−1858/−1567 bp) | |
Sense | 5-′TGAGATGAACAGCCCACAAA-3′ |
Antisense | 5′-TGCTCAGTCCTCATGACAGG-3′ |
Mutated sequences are underlined.