Barley possesses an indeterminate "spike"-type inflorescence that forms basic floral structures, called spikelets, in a distichous pattern along its central axis (termed rachis). Each rachis node in the barley spike produces three (one central and two lateral) spikelets.
The end of spikelet primordia initiation along the rachis marks the stage of maximum yield potential. Subsequently, the inflorescence meristem dome starts to collapse, followed by gradual basipetal degeneration of spikelet primordia and spikelets until a specific position along the spike is reached.
"We show that up to 50% of the initiated floral primordia are aborted before anthesis, representing an untapped yield potential," says Prof. Dr. Thorsten Schnurbusch, head of IPK's research group Plant Architecture. "Understanding the molecular underpinnings of spike PTD may thus help improve grain yield in cereals."
A study on this topic is published in The Plant Cell.
Due to its quantitative nature and environmental sensitivity, inflorescence PTD constitutes a complex mechanism affecting final grain number. This mechanism appears to be predictable and heritable, consistent with a developmental program.
Photosynthesis, immature spike greening, and energy metabolism appear to be significant contributors to proper spikelet growth and differentiation, and were restricted to basal and central spike parts. The researchers discovered, however, that the degenerating apical spike region undergoes sugar and amino acid depletion along with enhanced abscisic acid biosynthesis and signaling.
"Moreover, we functionally validated one of the apically expressed transcription factor genes, barley GRASSY TILLERS1 (HvGT1), an ortholog of maize GT1, as a growth repressor of apical spikelet development," emphasizes Nandhakumar Shanmugaraj, first author of the study.
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