Abstract

The extraordinarily long stigmatic silks of corn (Zea mays L.) are critical for grain production but the biology of their growth and emergence from husk leaves has remained underexplored. Accordingly, gene expression was assayed for inbreds 'B73' and 'Mo17' across five contiguous silk sections. Half of the maize genes (∼20,000) are expressed in silks, mostly in spatiotemporally dynamic patterns. In particular, emergence triggers strong differential expression of ∼1,500 genes collectively enriched for gene ontology terms associated with abiotic and biotic stress responses, hormone signaling, cell-cell communication, and defense metabolism. Further, a meta-analysis of published maize transcriptomic studies on seedling stress showed that silk emergence elicits an upregulated transcriptomic response that overlaps strongly with both abiotic and biotic stress responses. Although the two inbreds revealed similar silk transcriptomic programs overall, genotypic expression differences were observed for 5,643 B73-Mo17 syntenic gene pairs and collectively account for>50% of genome-wide expression variance. Coexpression clusters, including many based on genotypic divergence, were identified and interrogated via ontology-term enrichment analyses to generate biological hypotheses for future research. Ultimately, dissecting how gene expression changes along the length of silks and between husk-encased and emerged states offers testable models for silk development and plant response to environmental stresses.

Highlights

  • As stigmatic organs, maize silks are required for ovule fertilization, which occurs ∼7 × 1015 times annually as part of global corn grain production

  • transcript-length-normalized reads per million reads (RPKM) values were computed with the corresponding reference genome in each case

  • Examination of these data indicates that similar numbers of genes were expressed in the two inbreds in each of the five silk sections

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Summary

Introduction

Maize silks are required for ovule fertilization, which occurs ∼7 × 1015 times annually as part of global corn grain production. Maize yields depend on the successful emergence of silks from the husk leaves that protectively encase the ear (Bolaños & Edmeades, 1996) and on the sustained viability of silks for pollen reception under harsh environmental conditions after emergence (Bassetti & Westgate, 1993). To overcome the first of these challenges, silks grow more than 1 cm d–1 for 10 to 15 d until emergence from the husk leaves, after which cellular elongation continues at lesser rates (Fuad-Hassan, Tardieu, & Turc, 2008). Silks exhibit a high level of phenotypic variability in emergence rates across diverse germplasm under drought (Bolaños & Edmeades, 1996), as well as differences in susceptibility to different pathogens (Lübberstedt, Klein, & Melchinger, 1998) and pests (Abel, Wilson, Wiseman, White, & Davis, 2000; Lopez et al, 2019). The composition of many specialized metabolites varies among cultivars, including maysin (Byrne et al, 1996; Szalma, Buckler, Snook, & McMullen, 2005) and cuticular lipids (Dennison et al, 2019; Loneman et al, 2017; Perera et al, 2010)

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