This paper examines the story generation capabilities of generative AI, which are increasingly utilized across various industries. The narrative of the classic novel Don Quixote was input into ChatGPT, a generative AI model, and reconstructed through natural language prompts that applied the MacGuffin technique to create new story structures. The AI-generated narratives, produced in the forms of synopses and scene-by-scene treatments, were compared with the original work to evaluate narrative completeness. Furthermore, the reconstructed narratives were transformed into screenplay and game event formats to assess their potential applications in various media content. The results indicate that generative AI achieved meaningful outcomes in restructuring the original story into a reversal-based narrative using the MacGuffin structure. It also demonstrated sufficient capability to adapt stories for character dialogues and scene direction. Therefore, this paper suggests that generative AI can function as a supportive tool for human writers in the idea development and pre-production stages of screenplay and digital content creation.

게임플레이는 플레이어가 게임과 상호작용을 진행하면서 게임 상황에 대한 판단과 행동의 일련의 과정의 반복이라고 볼 수 있다. 잘 설계된 게임플레이는 플레이어로 하여금 게임에 몰입하도록 유도하며, 지속적으 로 몰입상태를 유지할 수 있도록 한다. RPG에서 게임플레이의 핵심과정중 하나는 몬스터와 상호작용하는 것이다. 일반적인 RPG의 몬스터는 패턴플레이로 구성되어 반복적으로 플레이가 진행되는 상황에서 지루함 을 유발하는 요인으로 작용한다. 이로 인해 게임을 플레이하는 플레이어중 고 레벨 플레이어는 레벨업을 위 해 습득해야 하는 경험치의 양의 증가로 인해 같은 필드에서 같은 몬스터를 오랜 시간동안 플레이하는 것 이 일반적이어서 시간이 지날수록 투자한 시간과 성취욕구 사이에서 만족도가 떨어지는 문제점이 발생한다. 본 연구에서는 플레이어의 성장과정에서 몬스터가 제공하는 정보에 대한 위계의 설정을 통하여 플레이어의 인지과정에 패턴의 변수를 인식하게 하여 다양한 게임플레이가 가능하도록 하며 이를 바탕으로 플로우 (Flow) 과정에서 경험하는 지루함의 요소를 극복하고 지속적으로 몰입과정을 느낄 수 있도록 한다.

Genome sequencing researches for considerable numbers of crops and wild plants are being developed. Cytogenetic researches according to chromosome number and size are essential to confirm and comprehend ploidy level and genome size before genome sequencing project is actually conducted. Cytogenetic researches on six food crop plants were carried out by DAPI staining and fluorescence in situ hybridization (FISH) method. Fagopyrum esculentum Moench showed 2n=2x=16, each chromosome length of 1.42㎛ to 1.77㎛, total chromosome length of 13.31㎛, and karyotypic formula of 2n=8m; Phaseolus angularis W.F. Wight, 2n=2x=22, 2.01㎛ to 3.84㎛, total 28.03㎛, 2n=9m+2sm, Perilla frutescens var. japonica Hara, 2n=2x=40, 1.73㎛ to 2.76㎛, total 44.36㎛, 2n=5m+13sm+2st. Chromosome sizes of the other three species such as, Panicum miliaceum L., 2n=2x=36, total chromosome length of 30.83㎛, Sesamum indicum L., 2n=2x=26, 27.39㎛, lpomoea batatas L., 2n=2x=30, total 33.51㎛ were too small for each chromosome type to be identified and analyzed. The result of FISH analysis using 5S and 45S rDNA probe showed species-specific chromosome locations in the genome. These preliminary analyses were carried out to decide which food crop to prioritize for genome sequencing. This work was supported by the “Cooperative Research Program for Agriculture Science & Technology Development (No.PJ009837), Rural Development Administration, Republic of Korea.

Cryopreservation has been known as an efficient method for long-term preservation of clonally propagated plants, and several cryopreservation methods have been developed. Among them, a droplet-vitrification method for potato using axillary shoot tips in vitro has been established previously. In this study, we have optimized the procedure in which explants were submitted to a step-wise pre-culture in liquid sucrose-enriched medium (0.3 and 0.7 M for 7 and 17 h, respectively). The pre-cultured explants were dehydrated with PVS3 (w/v, 50% glycerol + 50% sucrose) for 90 min or modified PVS2 vitrification solution (w/v, 37.5% glycerol + 15% DMSO + 15.0% ethylene glycol + 22.5% sucrose) for 30 min. This two dehydration solutions produced post-cryopreservation regeneration percentages of 57.2% and 80.9%, respectively. We also compared a new post-culture medium (0.1 mg L ･ -1 GA3, 0.1 mg L ･ -1 kinetin) with the conventional one (0.15 mg L ･ -1 IAA, 0.2 mg L ･ -1 zeatin, 0.05 mg L ･ -1 GA3); the shooting initiation rates were 80.9% and 43.5%, respectively. The results suggest that the modified droplet-vitrification protocol described in this study is more effective, easier to implement, and more economical than the droplet-vitrification protocols currently used for potato.