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. 2020 Nov 16;11:600820. doi: 10.3389/fpls.2020.600820

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Copyright © 2020 Fu, Wang, Shen, Zhang, Higgins and Liang.

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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DMC1and RAD51A are not able to load on meiotic chromosomes in osbrca2-1. (A) Immunolocalization of DMC1 (red) and OsREC8 (green) in wild-type and osbrca2-1 meiocytes at zygotene. (B) Immunolocalization of RAD51A (red) and OsREC8 (green) in wild-type and osbrca2-1 meiocytes at zygotene. (C) Statistical analysis of the number of OsDMC1 foci per cell in wild type (n = 28) and osbrca2-1 mutants (n = 26). (D) Statistical analysis of the number of OsRAD51A foci per cell in wild type (n = 33) and osbrca2-1 mutants (n = 32). All values represent the mean ± SD, ^***p < 0.0001, Student’s t tests. Bars = 2 μm.