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

Table 7.

In Silico Promoter Analysis of the 5 Zyxin-Dependent Candidate Genes for Putative PyPu Binding Sites

Gene Matrix Start End C.S M.S Sequence
CyclinE2 V$HSF1.04 −663 −687 1 0.851 caaagcttctctgggagcTTCTctg
ITGA8 V$HSF1.04 −3817 −3841 1 0.791 gttgaagcctcaggatccTTCTctc
V$HSF1.04 −3522 −3546 1 0.761 accccttatgaaggaaacTTCTctc
MMP13 V$HSF1.04 −3761 −3785 0.85 0.838 tttacatattcttaaaatTTCAatc
RGS5 V$HSF1.04 −3577 −3601 0.973 0.805 tagagataatctccaaagTTCCatg
V$HSF1.04 −2489 −2513 1 0.779 tggggtccttcttgttggTTCTatg
V$HSF1.04 −1621 −1645 1 0.775 tgcaggctgtcctcaaacTTCTgtt
V$HSF1.04 −236 −260 1 0.789 gggcatgtttctggtggcTTCTgtc

In silico promoter analysis of the 5 zyxin-dependent candidate genes for putative PyPu binding sites. Putative binding sites which remotely resemble the PyPu box are tabulated. The HSF has some similarity to the PyPu sequence but a prominent and reproducible stretch of pyrimidines was not detectable compared to that observed in ECs.4 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; ECs, endothelial cells; HSF, heat shock factor; ITGA8, integrin α8; M.S, matrix similarity; MMP13, matrix metalloproteinase 13; RGS5, regulator of G-protein signaling 5.