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. 2020 Mar 30;13:188. doi: 10.1186/s13104-020-05035-z

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Sequences of tested Ugt86Dd alleles. The top panel shows a fraction of exon 2 from the gene. The leftmost “T” (rightmost “C”) corresponds to position 3R: 11127665 (3R: 11127626) in Release 6 of the D. melanogaster reference genome. The bottom panel shows the predicted polypeptide sequences resulting from strains containing deletions. The “TAC” codon results in the “Y” amino acid (both highlighted in yellow). A3 and A4 are inbred, but wild-derived, strains [3]. A4-Ugt86Dd^wt, A4-Ugt86Dd^Del1, and A4-Ugt86Dd^Del11 were generated by Highfill et al. [6]. Four versions of A4-Ugt86Dd^Del22 (13H, 17B, 23C, and 26I) are identical for this region of the genome, and are new to the present study