The determination of spike architecture is critical to grain yield in wheat (Triticum aestivum), yet the underlying mechanisms remain largely unknown. Here, we measured 51 traits associated with spike architecture and floral development in 197 wheat accessions with photoperiod sensitive and insensitive alleles. We included five distinct allele combinations at the Photoperiod-1 (Ppd-1) loci. A systematic dissection of all recorded phenotypes revealed connections between floral development, spike architecture and grain yield. Modifying the durations of spikelet primordia initiation did not necessarily affect spikelet number. In addition, Ppd-1 loci clearly influenced rachis dry weight, pointing to the rachis vascular system as a potential target for higher yield. Ppd-1 displayed opposite effects on the durations of pre and post-anthesis phases. Ppd-1 controlled carpel size, but not anther size. Finally, the photoperiod-insensitive alleles of Ppd-1 triggered floral degeneration. In parallel, we profiled the spike transcriptome at six stages and four positions in three Ppd-1 genotypes which consists of 234 samples. Integrating phenotypic and expression data suggested that loss of function in Ppd-1 loci delayed floral degeneration by regulating autophagy and extended floret development by regulating genes in different families. Therefore, we concluded that Ppd-1 remodels spike architecture by regulating floral development in wheat. Appleyard, 1987). During WA stage, the meristematic dome initiates 7-9 floret primordia within each individual spikelet (1-3 primordia fewer than the maximum number) (Kirby and Appleyard, 1987). The lemmas of florets 1 and 2 at the base of the spikelet completely enclose the anther and ovary (Kirby and Appleyard, 1987). At the GA stage, the meristematic dome completes the initiation of floret primordia, so that after this stage no more floret primordia will be produced ; the glumes almost completely cover all but the tips of the florets. The spike length peaks at the YA stage (Guo et al., 2018); glumes are fully formed, and the lemmas of the first three florets are visible. At the TP stage, the first awn is visible (Zadoks et al., 1974), at HD stage, half of the spike emerges from the last leaf blade (Zadoks et al., 1974). Finally, at the AN stage, yellow anthers appear along the spike (Zadoks et al., 1974).Spike architecture is a complicated trait, that is determined by multiple factors. Spike fertility index (i.e. the ratio between grain number per spike and weight of spike chaff) is a critical metric of assimilate distribution between grains and spike chaff (e.g. glume, lemma, palea, rachis). Grain number per spikelet along the main inflorescence also influences spike shape. Spikelet density (the ratio between spike length and spikelet number) also indicates spike compactness. Spikelet fertility (the ratio between fertile and total spikelet number) informs on the proportion of aborted spikelets. In addition, grain size traits (thousand-kernel weight-TKW, grain area, grain width, grain le...