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Summary  Sexual reproduction in flowering plants offers a number of remarkable aspects to developmental biologists. First, the spore mother cells – precursors of the plant reproductive lineage – are specified late in development, as opposed to precocious germline isolation during embryogenesis in most animals. Second, unlike in most animals where meiosis directly produces gametes, plant meiosis entails the differentiation of a multicellular, haploid gametophyte, within which gametic as well as non‐gametic accessory cells are formed. These observations raise the question of the factors inducing and  modus operandi  of cell fate transitions that originate in floral tissues and gametophytes, respectively. Cell fate transitions in the reproductive lineage imply cellular reprogramming operating at the physiological, cytological and transcriptome level, but also at the chromatin level. A number of observations point to large‐scale chromatin reorganization events associated with cellular differentiation of the female spore mother cells and of the female gametes. These include a reorganization of the heterochromatin compartment, the genome‐wide alteration of the histone modification landscape, and the remodeling of nucleosome composition. The dynamic expression of  DNA  methyltransferases and actors of small  RNA  pathways also suggest additional, global epigenetic alterations that remain to be characterized. Are these events a cause or a consequence of cellular differentiation, and how do they contribute to cell fate transition? Does chromatin dynamics induce competence for immediate cellular functions (meiosis, fertilization), or does it also contribute long‐term effects in cellular identity and developmental competence of the reproductive lineage? This review attempts to review these fascinating questions.

Chromatin dynamics during cellular differentiation in the female reproductive lineage of flowering plants