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. Author manuscript; available in PMC: 2010 Apr 16.
Published in final edited form as: Curr Genet. 2008 Oct 3;54(6):283–299. doi: 10.1007/s00294-008-0217-7

Table 1.

Oligonucleotides used in this study

Gene Forward primera (5′ to 3′) Reverse primer (5′ to 3′) Product
(bp)
(a) Degenerate primer pairs used to amplify fragments of reference genes
act1 GTIGCICCIGARGARCAYCCI ACRTCIACRTCRCAYTTCAT 548
gpd1 GTIAARATHGTIAAYGAYAAYTT GCIACIACISWITRYTCIGGYTT 873
tef1 GTCCTCAGTCTTGTCATTTTTTTTCCT GGAGGGGCCTGTCTGTGGGAC 906
sar1 CTCGACAAYGCCGGAAAGAC TTGCCAAGGATGACAAAGGGG 833
28S GGAACCTTTCCCCACTTC AGTACCCGCTGAACTTAA 1,461
(b) Primer pairs used for quantification of transcripts by real-time PCR
gpr1 TTGATCCAGACCTTCATGCCAGC CATAAAAGGCCGCGACACGAA
gpr2 CTGCCCTCGTGTACATCTTCC GCCTTCAGATGAGTGAAAGTCG
gpr3 GCCAGCATTGGAACCATCATCG CCCAACACCAGATCGTAGCTCCA
gpr4 ATTCTAACTGGAGCCTGGTC GTACTTTGTGGCTCTGGTTG
act1 GCACGGAATCGCTCGTTG TTCTCCACCCCGCCAAGC
gpd1 CGTCGTAGTCCTTGTGGTTGACACC TCCTCCCACGGTCTCTTCAAGG
sar1 CTCGACAATGCCGGAAAGACCA TTGCCAAGGATGACAAAGGGG
tef1 TACTTCCCAGGCTGACTGCGCTAT GGAGGGGCCTGTCTGTGGGAC
28S TTTGAGTAAGAGCATACGGGGCC GTTGATACATTCGAATGCCCACGT
a

R = A or G, Y = C or T, I = inosine (panel A)