The findings establish seeds as a transcriptionally complex organ with high cell type heterogeneity and provide a basis for investigating the differentiation of diverse cell layers and spatial transcript profiles.
Abstract
• Seeds are complex reproductive organs consisting of diverse maternal and filial tissues. During development, the embryo and specialized tissues for nutrient storage required for seed germination and early seedling establishment emerge. • To explore the cellular diversity and differentiation of seeds, we performed single cell RNA-sequencing on heart stage Arabidopsis seeds and identified 20,097 cells that were grouped into ≥21 distinct cell clusters. 20 of the 21 clusters were spatially assigned by combining bioinformatic analysis, imaging reporter fusion marker lines, and spatial transcriptomics. • Our analysis revealed a high degree of differentiation of epidermal cell and inner cell layers along the rotational and axial seed axes, highlighting the importance of cell position and ontogenesis. We identified unexpected spatial domains, including a cluster marked by abscission zone-specific transcripts, and a nucellar cluster shaped by developmentally programmed cell death. Surprisingly, embryo and endosperm showed similarities in transcript profiles despite distinct and complementary functions. • In summary, our findings establish seeds as a transcriptionally complex organ with high cell type heterogeneity and provide a basis for investigating the differentiation of diverse cell layers and spatial transcript profiles.
This study provides a single-cell resolution framework for understanding early rice seed development, identifies the embryo-endosperm interface as an important cellular domain associated with embryogenesis, and offers a valuable resource for dissecting the molecular basis of seed formation in rice and related cereals.
Yingxiang Liu, Haoyuan Wang, Min Xu et al.· Journal of Integrative Plant...· 0 citations
There is a dominant view that plants are shaped by the ability of their outermost cell layers to resist or yield to pressure from internal tissues. During stem development, outer tissues originate from the tunica layers of the shoot meristem, while inner tissues are produced by the rib zone (RZ), named after its distinctive pattern of transverse cell divisions. Despite over a century of studies, the interplay between inner and outer tissues in shaping the stem remains unclear. Here, we show that mutations in a subfamily of IQ domain (IQD) genes disrupt the orientation of cell divisions in the RZ and increase stem diameter in Arabidopsis. Measurements of cell geometry, growth of marked cell clones, tissue-specific expression, and subcellular localization all support the idea that these IQD proteins reduce longitudinal cell divisions in the RZ, limiting the build-up of vertical cell files in inner tissues and the concomitant radial growth of the stem. Thus, the characteristic orientation of cell divisions in the RZ is important for shaping the stem, and the genetic control of organ shape can be exerted in inner plant tissues.
Bryony Yates, Emma McKechnie-Welsh, Nico Mol et al.· Current Biology· 1 citation
The domestication of maize from teosinte involved dramatic remodeling of the ear, yet the cellular and genetic bases of this transformation remain unclear. Here, we generate a single-nucleus and spatial transcriptome atlas of developing maize and teosinte ears. Comparative analysis reveals divergence in cob-associated cell types, with enhanced cytokinin signaling and reduced growth-inhibitory signals collectively driving cob thickening and enlargement in maize. We further demonstrate that domestication expanded the spatial expression domain of key transcription factors in maize meristem cells, enhancing the potential for increasing kernel number. Additionally, we verified a major domestication gene, ZmSPD1, in which two nonsynonymous SNPs differentiate maize from teosinte and alter jasmonic acid (JA) levels in the ear, thereby suppressing spikelet abortion to effectively double kernel production. These findings provide a cell-resolved mechanistic framework for how cob architecture and kernel number were shaped during maize domestication, offering new insights into the formation of key agronomic traits.
Yuebin Wang, Ruijie Mao, Yu Liu et al.· bioRxiv· 0 citations
ERECTA signaling is identified as a local brake on embryonic stomatal cell maturation, discovering another way to push precocious stomatal cell maturation that results in a complex, partially mature cell state that provide insights into the limitations on cell embryonic cell maturation.
Yadhusankar Sasidharan, Vijay Suryavanshi, Pablo González-Suárez et al.· bioRxiv· 0 citations
This review synthesizes recent progress across diverse plant species and tissues, showing that gene expression is not only cell-type specific but also tightly organized by position within organs and developmental niches, establishing spatial gene expression as a fundamental organizing principle of plant development and physiology.
Yiqing Wang, Zhengzhi Tan, Nicole A Freeman et al.· Plant Communications· 0 citations