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. 2009 Jan;133(1):17–27. doi: 10.1085/jgp.200810133

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© 2009 Ingleby et al.

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jgp.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

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Figure 1. — Editing of the Shaker locus. (A) The Shaker locus transcription unit is shown with numbered exons (yellow), constitutive splice sites (solid lines), alternative splice sites (broken lines), and stop codons (asterisks). The position of conserved elements predicted to direct editing, e1–e3, is shown in red. (B) The position of Shaker editing sites 1–4 is depicted on a generic cartoon of Kv channel topology. (C) Developmental profile of editing in whole animals for sites 1–4 is shown for larval, pupal, and adult stages. Color code as in B.