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. 2011 Apr 26;6(4):e18853. doi: 10.1371/journal.pone.0018853

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Chen et al.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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(A) Multiple species alignment of the promoter region of sphinx. Top panel indicates relative position of INE-1 element (green line), 265 bp region (orange bar) used in GFP transformation and additional 802 bp (pink bar) for 1067bp construct. Lower panel: sequence conservation of promoter region, black shade indicates conserved region. (B). Segregating sites in D. melanogaster. The nucleotide positions from the transcription start site are indicated in the first column. The second column shows the consensus nucleotides. The dots indicate that the nucleotides are identical to those of the consensus. The blue color represents the common haplotype. The first row contains the line numbers that were sequenced: 1. TWN.4 2. Yep2 3. Yep25 4. Ok17 5. HG84 6. Yep10 7. NFS 8. La79 9. TWN30 10. TWN35 11. TWN38 12. ZS30 13. ZS56 14. TWN 27.