Significance: Maize was domesticated from teosinte in Southern Mexico roughly 9,000 years ago. Maize originally was sensitive to photoperiod and required short-day conditions to flower. Thus, the reduced sensitivity to photoperiod is prerequisite for maize spread to long-day temperate regions. A gene encoding a CCT domain-containing protein, ZmCCT , was found by many researchers to modulate photoperiod sensitivity. The current study shows that insertion of a CACTA-like transposon into the ZmCCT promoter can suppress the ZmCCT expression remarkably and thus attenuates maize sensitivity under long-day conditions. The transposable element (TE) insertion event occurred in a tropical maize plant and has been selected for and accumulated as maize adapted to vast long-day environments. This selection leaves behind a TE-related linkage disequilibrium block with the very-low-nucleotide variations.

In rice (Oryza sativa), the presence of a dominant Badh2 allele encoding betaine aldehyde dehydrogenase (BADH2) inhibits the synthesis of 2-acetyl-1-pyrroline (2AP), a potent flavor component in rice fragrance. By contrast, its two recessive alleles, badh2-E2 and badh2-E7, induce 2AP formation. Badh2 was found to be transcribed in all tissues tested except for roots, and the transcript was detected at higher abundance in young, healthy leaves than in other tissues. Multiple Badh2 transcript lengths were detected, and the complete, full-length Badh2 transcript was much less abundant than partial Badh2 transcripts. 2AP levels were significantly reduced in cauliflower mosaic virus 35S-driven transgenic lines expressing the complete, but not the partial, Badh2 coding sequences. In accordance, the intact, full-length BADH2 protein (503 residues) appeared exclusively in nonfragrant transgenic lines and rice varieties. These results indicate that the full-length BADH2 protein encoded by Badh2 renders rice nonfragrant by inhibiting 2AP biosynthesis. The BADH2 enzyme was predicted to contain three domains: NAD binding, substrate binding, and oligomerization domains. BADH2 was distributed throughout the cytoplasm, where it is predicted to catalyze the oxidization of betaine aldehyde, 4-aminobutyraldehyde (AB-ald), and 3-aminopropionaldehyde. The presence of null badh2 alleles resulted in AB-ald accumulation and enhanced 2AP biosynthesis. In summary, these data support the hypothesis that BADH2 inhibits 2AP biosynthesis by exhausting AB-ald, a presumed 2AP precursor.

Summary: A major resistance quantitative trait locus, qRfg1, significantly enhances maize resistance to Gibberella stalk rot, a devastating disease caused by Fusarium graminearum. However, the underlying molecular mechanism remains unknown. We adopted a map‐based cloning approach to identify the resistance gene at qRfg1 and examined the dynamic epigenetic changes during qRfg1‐mediated maize resistance to the disease. A CCT domain‐containing gene, ZmCCT, is the causal gene at the qRfg1 locus and a polymorphic CACTA‐like transposable element (TE1) c. 2.4 kb upstream of ZmCCT is the genetic determinant of allelic variation. The non‐TE1 ZmCCT allele is in a poised state, with predictive bivalent chromatin enriched for both repressive (H3K27me3/H3K9me3) and active (H3K4me3) histone marks. Upon pathogen challenge, this non‐TE1 ZmCCT allele was promptly induced by a rapid yet transient reduction in H3K27me3/H3K9me3 and a progressive decrease in H3K4me3, leading to disease resistance. However, TE1 insertion in ZmCCT caused selective depletion of H3K4me3 and enrichment of methylated GC to suppress the pathogen‐induced ZmCCT expression, resulting in disease susceptibility. Moreover, ZmCCT‐mediated resistance to Gibberella stalk rot is not affected by photoperiod sensitivity. This chromatin‐based regulatory mechanism enables ZmCCT to be more precise and timely in defense against F. graminearum infection.