A 65-kb deletion survey identifies a distal <i>cis-</i>regulatory region for red-light induction of <i>Ghd7</i>, a key rice floral repressor.

Abstract

The <i>Ghd7</i> (<i>Grain number, plant height, and heading date 7</i>) gene integrates red light signals and circadian rhythms to control floral repression under long-day conditions in rice. CRISPR/Cas9 systems were employed to create a series of deletion mutant lines in the upstream regions of <i>Ghd7</i>, covering a 65-kb genomic region from its transcription start site (TSS). These deletions ranged from 2 to 25 kb in size. Three deletion lines, those from 0 to -3 kb (0/-3 K), -20 to -40 kb (-20/-40 K), and -26 to -30 kb (-26/-30 K) from the TSS, resulted in early flowering, similar to <i>Ghd7</i> knockout lines. The -20/-40 and -26/-30 K lines exhibited a loss of acute <i>Ghd7</i> morning induction. Night-break experiments consistently supported these findings, suggesting that the key <i>cis-</i>regulatory region for red light responses was located within the 3.7-kb region in -26/-30 K. In seedlings of the 0/-3 K deletion line, which retains the -29 to -86 bp region, <i>Ghd7</i> showed a diurnal pattern similar to wild type. This suggests that the deleted region in 0/-3 K is dispensable for both circadian rhythms and red-light responses. Further analyses of two deletion lines within the -26/-30 K region allowed us to narrow down the core <i>cis-</i>regulatory elements, responsive to morning-light signals, within a 228-bp segment located at 28-kb upstream of the TSS in <i>Ghd7</i>.