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Polat, I.

Publications and source records attributed to Polat, I..

2 recordsLinked to original sources

A premitotic polarity program patterns the grass leaf epidermis

Transverse asymmetric cell divisions (ACDs) in grass leaf epidermal development produce large basal pavement cells and small apical specialised cells. These "patterning divisions" generate the long-short epidermal cell pattern that is distinctive of grasses. Here, we show that patterning divisions require premitotic basal polarisation of Bd-POLAR-LIKE1 (BdPL1) in the model grass Brachypodium distachyon. Loss of BdPL1 disrupted division-plane orientation and postmitotic cell-size asymmetry in all cell files, which resulted in epidermal patterning defects. Ectopic expression analyses demonstrated that BdPL1 polarisation was independent of cellular context and sufficient to promote supernumerary transverse divisions. Furthermore, the developmental regulators BdBREVIS RADIX-solo and BdYODA1 formed a post-division polarity domain enforcing cell fate asymmetry independently of BdPL1. We propose that the premitotic BdPL1 module enforces physical cell-division asymmetry contributing to medio-lateral patterning of cell types, whereas the postmitotic BdBRX-solo/ BdYDA1 module enforces within-file cell fate asymmetry. Together, they robustly pattern the grass leaf epidermis.

plant biology↗

Qualitative rather than quantitative phosphoregulation shapes the end of meiosis I in budding yeast

Exit from mitosis is brought about by dramatic changes in the phosphoproteome landscape. A drop in Cyclin-dependent kinase (Cdk), the master regulatory kinase, and activation of counteracting phosphatases such as Cdc14 in budding yeast, results in ordered substrate dephosphorylation, allowing entry into a new cell cycle and replication licensing. In meiosis however, two cell divisions have to be executed without intermediate DNA replication, implying that global phosphorylation and dephosphorylation have to be adapted to the challenges of meiosis. Using a global time-resolved phosphoproteomics approach in budding yeast, we compared the phosphoproteome landscape between mitotic exit and the transition from meiosis I to meiosis II. We found that unlike exit from mitosis, Cdk phosphomotifs remain mostly stably phosphorylated at the end of meiosis I, whereas a majority of Cdk-unrelated motifs are reset by dephosphorylation. However, inducing an artificial drop of Cdk at metaphase of meiosis I leads to ordered substrate dephosphorylation, comparable to mitosis, indicating that phosphoregulation of substrates at the end of meiosis I is thus mainly qualitatively rather than quantitatively ordered.

cell biology↗