PIRL6 knockdown disrupts female gametogenesis. A, Simplified diagram summarizing selected aspects of Arabidopsis female gametophyte development at the indicated developmental stages (Christensen et al., 1998), pictured with the micropyle at top and the chalazal end at bottom. The embryo sac is represented as a white oval and constituent nuclei as black circles. Adjacent sporophytic tissues are included: light gray, nucellus; dark gray, inner integument. A, Antipodal cell nuclei in their characteristic triangular configuration; CC, central cell nucleus; DN, distal nucellus region; M, megaspore nucleus. B, Ovules from ovaries at postmitotic developmental stages, cleared as whole mounts in Hoyer’s solution and viewed by DIC microscopy. The micropylar region (MP) of each ovule is labeled to indicate the orientation of the image. Parent plants were hemizygous for the PIRL6-KD construct, and embryo sacs segregated approximately 50% for PIRL6 knockdown. The top row shows a wild-type ovule (WT) and three examples of segregating PIRL6-KD ovules from FG6 stage ovaries. Antipodal cells (ACs), a large vacuole (V), the central cell (CC), and the cluster of egg cell and synergids (E+S) were discernible in segregating wild-type ovules (nuclei are not visible in the selected focal plane). PIRL6-KD embryo sacs each feature single, apparently mitotically arrested cells (white arrows) with large nuclei, surrounded by an abnormally persistent, sharply defined distal nucellus layer (DN). Integument (IN) layers fully envelope the PIRL6-KD gametophytes, despite their developmental arrest as single cells (in contrast to the integuments flanking the wild-type single-cell FG1 ovule shown in Fig. 2B). The bottom row shows wild-type and PIRL6-KD ovules from FG5 stage ovaries. Yet-undifferentiated cells produced by mitotic divisions (Cs) and an initiating central vacuole (iV) are discernible in the FG5 wild-type ovule. PIRL6-KD embryo sacs resembled those observed in PIRL6-KD FG6 ovaries, with single, arrested cells (white arrows) enveloped by a persistent distal nucleus (DN) and expanded integuments (IN) that resembled those of wild-type ovules. Bars = 10 µm.