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Meiotic disturbances in F1 hybrids and their progenies are still major problems in wide hybridization. To investigate the genome affinity reflected in chromosome pairing and segregation, we studied chromosome behaviors during meiosis in two interspecific F1 hybrids [O. minuta × O. australiensis (Om × Oa, BCE genome) and Oa × O. ridleyi (Or, EHJ genome)] by using both traditional staining methods and genomic in situ hybridization (GISH). GISH analysis has been successfully performed on mitotic chromosomes to distinguish different Oryza genomes, but relatively fewer systematic analyses of meiotic chromosomes of interspecific hybrids have been reported. In the hybrids, highly irregular chromosome behaviors through meiosis resulted in producing microspores with unbalanced genome. At diakinesis of these two hybrids, most chromosomes present as univalent, with low frequency as bivalents and occasionally as trivalents. In a pollen mother cell, 2 to 8 bivalents and 0 to 4 trivalents were observed in the hybrid Oa × Or, and 1 to 8 bivalents and 0 to 5 trivalents were observed in the hybrid Om × Oa. GISH results indicated that 51.52% bivalents in Oa × Or and 79.65% bivalents in Om × Oa involved allosyndetic association, which indicates that recombination and introgression should be possible if viable backcrosses can be recovered even from triploid hybrids. In this study, we revealed that the meiotic disturbance due to low affinities between parental genomes is the major reason for the sterility of these two triploid interspecific hybrids. The two hybrids showing vigor in reproductive growth are potential genetic resources in future breeding programs. A better understanding of genomic affinities between these distant Oryza species can facilitate planning an effective breeding program by using wide hybridization, and efficient and routine GISH analysis is helpful to monitor alien introgression in the process.

Wheat (Triticum aestivum L.) is an important crop and requires long day and short night to flower. To study the molecular mechanism of photoperiodic regulation of flowering in this species, we isolated a wheat TaGI1 gene, an ortholog of GIGANTEA (GI) in Arabidopsis. RNA blot hybridization revealed that TaGI1 is expressed in leaves in a rhythmic manner under long day and short day conditions and its rhythmic expression is regulated by photoperiods and circadian clocks. Further study demonstrated that the TaGI1 rhythmic expression in the leaves of seedlings is initiated by photoperiods, implying that TaGI1 does not show circadian regulation until after being entrained in a light/dark cycle. Interestingly, TaGI1 mRNA was detected in adaxial epidermal cells right above the vascular bundles of leaves, suggesting that the localization of TaGI1 transcripts in leaves may function to regulate flowering in response to photoperiods. Since overexpression of TaGI1 altered flowering time in wild type and complemented the gi mutant in Arabidopsis, it confirmed that TaGI1 is an ortholog of GI in Arabidopsis.