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Table 2 Names and sequences of the oligonucleoides used in the present work

From: Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans Progressiva

Name

Sequence of oligonucleotides used in this work

LTR-1F

CAAGTACTGTTACAGGACCC

Sph-1F

TGCTCCCACCTACTCCATCC

Prom-3Frev

GCCATGGGAGCTTACAGTG

067-F/REV

GAGGCGGAGTGCGAGGCAGC

6R

CGAAGGCAGCTAACTGTATC

1.2-F

(AGCTGGTACC)AGCCCCTCCATGCTTATTTC

0.7-F

(AGCTGGTACC)GCTCATAGCTTCCAC

0.6-F

(AGCTGGTACC)GGAGGAAATGATGTGTTGCTG

0.3-F

(AGCTGGTACC)GAAGTTTATTCTGCCC

0.16-F

(AGCTGGTACC)GCTGCAGCCACCGCAG

0.072-F

(AGCTGGTACC)CCGCAGAGTTCC

 

Oligonucleotides for site-directed mutagenesis

Fr072mut-F

CACCGCCCCGAACCGAACCGCGCCGAACCGCGCCGCG

Fr072mut-R

CGCGGCGCGGTTCGGCGCGGTTCGGTTCGGGGCGGTG

 

Oligonucleotides for EMSA

GC-emsa F

GCCCCGCCCCGCCCCGCGCCGCCCCGCG

GC-emsa R

GGCGCGGGGCGGCGCGGGGCGGGGCGGGG

GCmut-emsa F

GCCCCGAACCGAACCGCGCCGAACCGCG

GCmut-emsa R

GGCGCGGTTCGGCGCGGTTCGGTTCGGGG

  1. (agctggtacc) Extrabases and Kpn-1 recognition site (italic) to facilitate PCR products subcloning in the pGL3-basic Luciferase expression vector.