Abstract

In most eukaryotes, a set of conserved proteins that are collectively termed ZMM proteins (named for molecular zipper 1 [ZIP1], ZIP2, ZIP3, and ZIP4, MutS homologue 4 [MSH4] and MSH5, meiotic recombination 3, and sporulation 16 [SPO16] in yeast [Saccharomyces cerevisiae]) are essential for the formation of the majority of meiotic crossovers (COs). Recent reports indicated that ZIP2 acts together with SPO16 and ZIP4 to control CO formation through recognizing and stabilizing early recombination intermediates in budding yeast. However, whether this mechanism is conserved in plants is not clear. Here, we characterized the functions of SHORTAGE OF CHIASMATA 1 (OsSHOC1; ZIP2 ortholog) and PARTING DANCERS (OsPTD; SPO16 ortholog) and their interactions with other ZMM proteins in rice (Oryza sativa). We demonstrated that disruption of OsSHOC1 caused a reduction of CO numbers to ∼83% of wild-type CO numbers, whereas synapsis and early meiotic recombination steps were not affected. Furthermore, OsSHOC1 interacts with OsPTD, which is responsible for the same set of CO formations as OsSHOC1. In addition, OsSHOC1 and OsPTD are required for the normal loading of other ZMM proteins, and conversely, the localizations of OsSHOC1 and OsPTD were also affected by the absence of OsZIP4 and human enhancer of invasion 10 in rice (OsHEI10). OsSHOC1 interacts with OsZIP4 and OsMSH5, and OsPTD interacts with OsHEI10. Furthermore, bimolecular fluorescence complementation and yeast-three hybrid assays demonstrated that OsSHOC1, OsPTD, OsHEI10, and OsZIP4 were able to form various combinations of heterotrimers. Moreover, statistical and genetic analysis indicated that OsSHOC1 and OsPTD are epistatic to OsHEI10 and OsZIP4 in meiotic CO formation. Taken together, we propose that OsSHOC1, OsPTD, OsHEI10, and OsZIP4 form multiple protein complexes that have conserved functions in promoting class I CO formation.

Highlights

  • In most eukaryotes, a set of conserved proteins that are collectively termed ZMM proteins are essential for the formation of the majority of meiotic crossovers (COs)

  • Compared to HEI10 foci in the wild type at diakinesis (23.3, n 5 13, range 20–27), fewer foci were observed in osshoc1-2 (15.7, n 5 11, range 11–19) and osptd-1 (14.3, n 5 16, range 10–19; Fig. 8, C and D). These results suggest that OsSHOC1 and OsPTD are required for normal localization of OsMER3, OsZIP4, and OsHEI10

  • A further decrease in the number of COs was observed in the double mutant of OsSHOC1 and OsGEN1, the latter of which encodes a resolvase required for class II CO formation (Wang et al, 2017)

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Summary

Introduction

A set of conserved proteins that are collectively termed ZMM proteins (named for molecular zipper 1 [ZIP1], ZIP2, ZIP3, and ZIP4, MutS homologue 4 [MSH4] and MSH5, meiotic recombination 3, and sporulation 16 [SPO16] in yeast [Saccharomyces cerevisiae]) are essential for the formation of the majority of meiotic crossovers (COs). Recent reports indicated that ZIP2 acts together with SPO16 and ZIP4 to control CO formation through recognizing and stabilizing early recombination intermediates in budding yeast Whether this mechanism is conserved in plants is not clear. We propose that OsSHOC1, OsPTD, OsHEI10, and OsZIP4 form multiple protein complexes that have conserved functions in promoting class I CO formation. In budding yeast (Saccharomyces cerevisiae), synaptonemal complex (SC) assembly and interference-sensitive CO formation rely on a group of functionally related proteins consisting of molecular zipper 1 (ZIP1), ZIP2, ZIP3, ZIP4, MutS homologue 4 (MSH4), MSH5, meiotic recombination 3, and sporulation 16 (SPO16; ZMM proteins; Lynn et al, 2007; Shinohara et al, 2008). Osmsh4-osmsh mutants have the greatest reduction in Class I COs of the ZMMs accompanied by complete SC installation and may be required for normal localization of other ZMM proteins on chromosomes, indicating an upstream function (Luo et al, 2013; Zhang et al, 2014)

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