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Table 1 Primer sequences used in this study.

From: Sp1/Sp3 and DNA-methylation contribute to basal transcriptional activation of human podoplanin in MG63 versus Saos-2 osteoblastic cells

Name

Sequence (5'→3') a

Experiment b

hPP rev (+207/+178)

CACATCGTTCCCGTTGAGTTGTTGCTCTCC

RT-PCR

hPP 1 (+1/+19)

AACTGCAAAGTTTGCTGTC

RT-PCR

hPP 2 (-16/+3)

CGCTCGGAAAGTTCTCAAC

RT-PCR

hPP 3 (-35/-17)

GAGAGATAAATGCTGACTC

RT-PCR

hPP 4 (-52/-33)

CTCCCCCGCCTCCTCGGGA

RT-PCR

hPP 5 (-68/-50)

CTTGCGGCCGACCCCGCTC

RT-PCR

hPP 6 (-83/-65)

CCGGACGGAGACCACCTTG

RT-PCR

hPP 7 (-97/-79)

CGGGCCTAGCGCGCCCGGA

RT-PCR

hPP 8 (-108/-90)

GAGCCCGAGGGCGGGCCTA

RT-PCR

hPP 9 (-125/-107)

TTGGCGCCGGCCAAACAGA

RT-PCR

hPP rev (+114/+96)

AGCCTGGAGGAGCGCGAC

RT-PCR

FII (-1885/-1866)

GCAATGAGCTCATCCACTAACTCCTTCATCC

Cloning, LA

F I (-857/-840)

GCAATGAGCTCACGTAAGTTCTCTGGTTG

Cloning, LA

RII (-783/-803)

GCAATCTCGAGAATCCTCACTTTACTGGTTTA

Cloning

RI (+154/+171)

GCAATCTCGAGCCGAGCAGCAAGATTCTG

Cloning, LA

F1 (-1642/-1616)

TTGAATAAAGCGGGCCATC

LA

F2 (-1378/-1360)

TCATCTTCTAGGTTCAGGT

LA

F3 (-1104/-1086)

ACAATCTCTCCTGTGATTC

LA

F4 (-666/-658)

ACAGCATCGCAGCGCTGGA

LA

F5 (-498/480)

ACCAGCGCGGGCCGCCTCT

LA

F6 (-361/-343)

CACTTCTGCCCATAACAAG

LA

F7 (-261/-243)

AACCCCGTTTGTTGCATGT

LA

F8 (-232/-214)

CCTCCTGTTGTTGAGCAGA

LA

F9 (-186/-168)

AGTCCTGGCGGCCCCCGCA

LA

F10 (-159/-141)

CCTGTAACTTTAAACCTGG

LA

F11 (-114/-96)

CAAACAGAGCCCGAGGGCG

LA

F12 (-76/-58)

GAGACCACCTTGCGGCCGA

LA

F13 (-38/-20)

CGGGAGAGATAAATGCTGA

LA

F14 (-26/-8)

ATGCTGACTCCGCTCGGAA

LA

fp 1

CCGCTCCCCCGCCTCCT CGGGA

EMSA

fp 1 mut

CCGCTCCA CATAA TCCTCGGGA

Mutation

fp 2

GAGCCCGAGGGCGGG CCTAGCG

EMSA

fp 2 mut

GAGCCCGAT GATAA GCCTAGCG

Mutation

fp 3

GATCATCGTTTTGGCGCCGGC CAA

EMSA

fp 4

CAGATGACGGCCAACTTTTTTTGTTTTTAAGCCATCAAA

EMSA

fp 5

CCAAACTCCCCCCACC AGCCAG

EMSA

fp 5 mut

CCAAACTCTA CAG ACCAGCCAG

Mutation

fp 6

TTTTCAAAACTGCCAAAGCC

EMSA

fp 7

CACCGCTTGGCCCGGCCTAATCC

EMSA

fp 7 mut

CACCGCTTGGAT CTTG CCTAATCC

Mutation

fp 8

GGACACAGGTTTGCGACCAGGACGGT

EMSA

Bis-fwd 1

GTTAGGGTTTGTAGTTTTGGTGG

BS

Bis-rev 1

CACCACAACCACAAACCCAACCT

BS

Bis-fwd 2

GAGGGTGAATTAGGTTTGGAAGGGG

BS

Bis-rev 2

CAACCCACACTAATCAATTACACCC

BS

Bis-fwd 3

GAGTTGTTGGTTTTATTTGGTTTAGGAGGGTGAG

BS

Bis-rev 3

CTATTCTACTTATATATAACTCCAAAATCACACAC

BS

  1. a Sequences protected in DNase I footprinting are underlined; mutated nucleotides are indicated in bold italics.
  2. b RT-PCR, reverse transcription PCR; LA, Luciferase assay; EMSA, electrophoretic mobility shift assay; BS, bisulfite sequencing.