A cytological framework of female meiosis in Arabidopsis

preprint OA: closed
📄 Open PDF Full text JSON View at publisher

Abstract

Summary Female and male meiosis often differ in many aspects, such as their duration and the frequency as well as the positioning of crossovers. However, studying female meiosis is often very challenging and thus, much less is known about female versus male meiosis in many species including plants. To approach this gap, we have developed a live-cell imaging system for female meiocytes in Arabidopsis. This allowed us to obtain a temporally resolved cytological framework of female meiosis in the wildtype that serves as a guiding system for future studies. Here, we have applied this imaging system to study mutants in cyclin- dependent kinase inhibitors, in which a designated female meiocyte undergoes several mitotic divisions before entering meiosis. This enabled us to address when a meiocyte is committed to meiosis, a key question during reproductive development and in particular for the analysis of apomictic species in which meiosis is skipped. Highlights Establishment of a live-cell imaging system captures dynamic features of female meiosis. Identification of cytological landmarks ensures robust assignment of meiotic stages. Time-lapse imaging enables quantitative dissection of meiotic phases. Application of the framework reveals great plasticity in the commitment to meiosis.
Full text 1,374 characters · extracted from oa-doi-fallback · click to expand
Summary Female and male meiosis often differ in many aspects, such as their duration and the frequency as well as the positioning of crossovers. However, studying female meiosis is often very challenging and thus, much less is known about female versus male meiosis in many species including plants. To approach this gap, we have developed a live-cell imaging system for female meiocytes in Arabidopsis. This allowed us to obtain a temporally resolved cytological framework of female meiosis in the wildtype that serves as a guiding system for future studies. Here, we have applied this imaging system to study mutants in cyclin- dependent kinase inhibitors, in which a designated female meiocyte undergoes several mitotic divisions before entering meiosis. This enabled us to address when a meiocyte is committed to meiosis, a key question during reproductive development and in particular for the analysis of apomictic species in which meiosis is skipped. Highlights Establishment of a live-cell imaging system captures dynamic features of female meiosis. Identification of cytological landmarks ensures robust assignment of meiotic stages. Time-lapse imaging enables quantitative dissection of meiotic phases. Application of the framework reveals great plasticity in the commitment to meiosis. Competing Interest Statement The authors have declared no competing interest.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00