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. 2015 Jun 12;4(6):e001712. doi: 10.1161/JAHA.114.001712

Table 8.

In Silico Promoter Analysis of the 3 MRTF-A-Regulated Zyxin-Dependent Candidate Genes for Putative SRF Binding Sites

Gene Matrix Start End C.S M.S Sequence
CyclinE2 V$SRF.04 −2464 −2482 1 0.865 ctaacccgtTATGgcaaga
ITGA8 V$SRF.03 −2524 −2542 1 0.805 cttcacctatATGGactgc
V$SRF.05 −1053 −1071 1 0.816 ctagcctgagAAGGctgtg
V$SRF.02 −381 −399 1 0.868 tgttcCATAtgcggcgaga
V$SRF.04 −380 −398 1 0.925 ctcgccgcaTATGgaacac
MMP13 V$SRF.04 −2915 −2933 0.901 0.87 tggaccacaTAAGacccaa
V$SRF.02 −1737 −1755 1 0.851 gggctCATAtcagggccca
V$SRF.04 −1736 −1754 1 0.872 gggccctgaTATGagccct
V$SRF.05 −1423 −1441 1 0.838 ttgacctcaaAAGGgggag

In silico promoter analysis of the 3 MRTF-A-regulated zyxin-dependent candidate genes for putative SRF binding sites. Putative SRF binding sites are tabulated. A maximum C.S is obtained when there is a strong match between highly conserved bases of the matrix and the input sequence. A good match to the matrix or the M.S has a value >0.80. Promoter sequences ≈4000 bp upstream of the transcription start site were analyzed for this purpose. C.S indicates core similarity; ITGA8, integrin α8; M.S, matrix similarity; MMP13, matrix metalloproteinase 13; MRTF-A, myocardin-related transcription factor A; SRF, serum response factor.