Rice microtubule-associated protein OsMAP65-3.1, but not OsMAP65-3.2, plays a critical role in phragmoplast microtubule organization in cytokinesis

In plants, MAP65 preferentially cross-links the anti-parallel microtubules (MTs) and plays an important role for cytokinesis. However, the functions of MAP65 isoforms in rice ( Oryza sativa. L) are largely unknown. Here, we identified two MAP65-3 homologs in rice, OsMAP65-3.1 and OsMAP65-3.2. We fou...

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Veröffentlicht in:Frontiers in plant science 2022-10, Vol.13, p.1030247-1030247
Hauptverfasser: Lin, Xiaoli, Xiao, Yu, Song, Yongping, Gan, Cong, Deng, Xingguang, Wang, Peng, Liu, Jialong, Jiang, Zhishu, Peng, Limei, Zhou, Dahu, He, Xiaopeng, Bian, Jianmin, Zhu, Changlan, Liu, Bo, He, Haohua, Xu, Jie
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Sprache:eng
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Zusammenfassung:In plants, MAP65 preferentially cross-links the anti-parallel microtubules (MTs) and plays an important role for cytokinesis. However, the functions of MAP65 isoforms in rice ( Oryza sativa. L) are largely unknown. Here, we identified two MAP65-3 homologs in rice, OsMAP65-3.1 and OsMAP65-3.2. We found that both OsMAP65-3.1 and OsMAP65-3.2 were similar in dimerization and location to AtMAP65-3, and the expression of either rice genes driven by the AtMAP65-3 promoter suppressed the cytokinesis failure and growth defect of atmap65-3 . However, OsMAP65-3.1 with native promoter also recovered the atmap65-3 , but OsMAP65-3.2 with its own promoter had no effects. OsMAP65-3.1 but not OsMAP65-3.2 was actively expressed in tissues enriched with dividing cells. R1R2R3-Myb (MYB3R) transcription factors directly bound to the OsMAP65-3.1 promoter but not that of OsMAP65-3.2 . Furthermore, osmap65-3.2 had no obvious phenotype, while either osmap65-3.1 or osmap65-3.1(+/-) was lethal. The eminent MTs around the daughter nuclei and cytokinesis defects were frequently observed in OsMAP65-3.1 -defective plants. Taken together, our findings suggest that OsMAP65-3.1 , rather than OsMAP65-3.2 , plays essential roles in rice cytokinesis resulting from their differential expression which were passably directly regulated by OsMYB3Rs.
ISSN:1664-462X
1664-462X
DOI:10.3389/fpls.2022.1030247