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논문 기본 정보

자료유형
학술저널
저자정보
Park Jie Eun (Soonchunhyang University) Patnaik Bharat Bhusan (Soonchunhyang University) Sang Min Kyu (Soonchunhyang University) Song Dae Kwon (Soonchunhyang University) Jeong Jun Yang (Soonchunhyang University) Hong Chan Eui (Soonchunhyang University) Kim Yong Tae (Soonchunhyang University) Shin Hyeon Jun (Soonchunhyang University) Ziwei Liu (Soonchunhyang University) Patnaik Hongray Howrelia (Soonchunhyang University) Hwang Hee Ju (Soonchunhyang University) Park So Young (Nakdonggang National Institute of Biological Resources) Kang Se Won (Korea Research Institute of Bioscience and Biotechnology (KRIBB)) Ko Jung Ho (Korean National Police University) Lee Jun Sang (Soonchunhyang University) Park Hong Seog (Research Institute, GnC BIO Co., LTD) Jo Yong Hun (Soonchunhyang University) Han Yeon Soo (Chonnam National University) Lee Yong Seok (Soonchunhyang University)
저널정보
한국유전학회 Genes & Genomics Genes and Genomics Vol.46 No.7
발행연도
2024.7
수록면
851 - 870 (20page)
DOI
10.1007/s13258-024-01511-z

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Background The Bradybaenidae snail Karaftohelix adamsi is endemic to Korea, with the species tracked from Island Ulleung in North Gyeongsang Province of South Korea. K. adamsi has been classified under the Endangered Wildlife Class II species of Korea and poses a severe risk of extinction following habitat disturbances. With no available information at the DNA (genome) or mRNA (transcriptome) level for the species, conservation by utilizing informed molecular resources seems difficult. Objective In this study, we used the Illumina short-read sequencing and Trinity de novo assembly to draft the reference transcriptome of K. adamsi. Results After assembly, 13,753 unigenes were obtained of which 10,511 were annotated to public databases (a maximum of 10,165 unigenes found homologs in PANM DB). A total of 6,351, 3,535, 358, and 3,407 unigenes were ascribed to the functional categories under KOG, GO, KEGG, and IPS, respectively. The transcripts such as the HSP 70, aquaporin, TLR, and MAPK, among others, were screened as putative functional resources for adaptation. DNA transposons were found to be thickly populated in comparison to retrotransposons in the assembled unigenes. Further, 2,164 SSRs were screened with the promiscuous presence of dinucleotide repeats such as AC/GT and AG/CT. Conclusion The transcriptome-guided discovery of molecular resources in K. adamsi will not only serve as a basis for functional genomics studies but also provide sustainable tools to be utilized for the protection of the species in the wild. Moreover, the development of polymorphic SSRs is valuable for the identification of species from newer habitats and cross-species genotyping.

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