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Table 7 Verification of FPC contig assembly by PCR amplicons designed hybridization markers.

From: Genomic tools development for Aquilegia: construction of a BAC-based physical map

Marker

Homology

Primer sequences

# positive hits (# contigsa)

# positive hits with expected amplicons

Aq_SR_Ctg_2

mlp-like protein 28

Fwd AGGTGATGGAACCTGTGAGG Rev CACAATCCATGTCACCAAGC

14 (3 +3sb)

14

Aq_SR_Ctg_8

No homology

Fwd GGCTATATCCACCAGGCTGA Rev AAGGGCCAGCACTTTATCCT

12 (3)

10

Aq_SR_Ctg_22

Late embryogenesis-abundant protein

Fwd ATCATCCAACCTTGCGTTGT Rev GGGACCGGAACTATCCAAAT

12 (2)

12

Aq_SR_Ctg_30

Ubiquitin-conjugating enzyme E2

Fwd GCCCAAATCAAGAAACCAGA Rev CCTTTATGGACCCTGGATCA

8 (1)

8

Aq_SR_Ctg_118

putative staygreen protein

Fwd TGGGGTCCACTTAAAGATGC Rev GAGTTGGTTGGTTTGGTTCC

5 (3)

5

Aq_SR_Ctg_127

universal stress protein 1

Fwd AGTAACTGGGCAAGCAGCAT Rev ATGGTGATGCAAGGGAAAAA

6 (2)

6

Aq_SR_Ctg_133

ethylene-responsive transcriptional co-activator)

Fwd ATCGCATCGTCATCAAACAA Rev TTCAGCAGGCGTACGACGAG

4 (2)

3

Aq_SR_Ctg_144

Benzodiazepine receptor-related

Fwd ACACTACGACATGCCAACCA Rev TAGCCCAGCCCAACAAATAG

2 (1)

2

  1. aThe number of contigs where the positively hybridized BACs were located
  2. bMarker Aq_SR_Ctg_2 also hybridized to 3 singletons other than 11 clones in 3 different contigs