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. 2021 Jun 8;12:655267. doi: 10.3389/fpls.2021.655267

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Copyright © 2021 Fiol, García-Gómez, Jurado-Ruiz, Alexiou, Howad and Aranzana.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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(A) Alignment of PsMYB10.1 in silico translated proteins from a whole-gene sequence. Conserved amino acids (gray arrows) and signature motifs ([A/S/G]NDV; [R/K]Px[P/A/R]x2[F/Y]) from R2R3-MYB anthocyanin-promoting proteins from Rosaceae were detected in all PsMYB10.1 sequences (Lin-Wang et al., 2010). Conserved motif [D/E]Lx2[R/K]x3Lx6Lx3R indicates a possible interaction with basic-helix-loop-helix (bHLH) proteins. Black arrows indicate key residues in PpMYB10.1 function (Zhou et al., 2018). (B) Polymorphisms found between a356_H1, a356_H3, a470_H2, a470_H4, and a243 upstream sequences: (a) G-box motif in the 44 bp indel; (b) polymorphisms in the R1-motif (Espley et al., 2009); (c) SNP S3_12879559 (Salazar et al., 2017); and (e) 8 bp insertion in exon 1 of a243, 4 bases before an in-frame STOP codon (shadowed). The start codon is marked as (d).